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adipose tissue
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{{Redirect|Adipose|the fictional creature from Doctor Who|List of Doctor Who universe creatures and aliens (0–9, A–G)#Adipose}}{{see also|Fat}}







factoids
| Image = Illu connective tissues 1.jpg| Caption = Adipose tissue is one of the main types of connective tissue.| Width = | Image2 = | Caption2 = | Latin =| Greek =| Precursor = | System = | Artery = | Vein = | Nerve = | Lymph = }}In biology, adipose tissue, body fat, or simply fat is a loose connective tissue composed mostly of adipocytes.JOURNAL, Birbrair A, Zhang T, Wang ZM, Messi ML, Enikolopov GN, Mintz A, Delbono O, Role of pericytes in skeletal muscle regeneration and fat accumulation, Stem Cells and Development, 22, 16, 2298–314, August 2013, 23517218, 3730538, 10.1089/scd.2012.0647, In addition to adipocytes, adipose tissue contains the stromal vascular fraction (SVF) of cells including preadipocytes, fibroblasts, vascular endothelial cells and a variety of immune cells such as adipose tissue macrophages. Adipose tissue is derived from preadipocytes. Its main role is to store energy in the form of lipids, although it also cushions and insulates the body. Far from being hormonally inert, adipose tissue has, in recent years, been recognized as a major endocrine organ,JOURNAL, Kershaw EE, Flier JS, Adipose tissue as an endocrine organ, The Journal of Clinical Endocrinology and Metabolism, 89, 6, 2548–56, June 2004, 15181022, 10.1210/jc.2004-0395, as it produces hormones such as leptin, estrogen, resistin, and cytokine (especially TNFα). The two types of adipose tissue are white adipose tissue (WAT), which stores energy, and brown adipose tissue (BAT), which generates body heat. The formation of adipose tissue appears to be controlled in part by the adipose gene. Adipose tissue â€“ more specifically brown adipose tissue â€“ was first identified by the Swiss naturalist Conrad Gessner in 1551.JOURNAL, Cannon B, Nedergaard J, Developmental biology: Neither fat nor flesh, Nature, 454, 7207, 947–48, August 2008, 18719573, 10.1038/454947a, 2008Natur.454..947C,

Anatomical features

In humans, adipose tissue is located: beneath the skin (subcutaneous fat), around internal organs (visceral fat), in bone marrow (yellow bone marrow), intermuscular (Muscular system) and in the breast tissue. Adipose tissue is found in specific locations, which are referred to as adipose depots. Apart from adipocytes, which comprise the highest percentage of cells within adipose tissue, other cell types are present, collectively termed stromal vascular fraction (SVF) of cells. SVF includes preadipocytes, fibroblasts, adipose tissue macrophages, and endothelial cells. Adipose tissue contains many small blood vessels. In the integumentary system, which includes the skin, it accumulates in the deepest level, the subcutaneous layer, providing insulation from heat and cold. Around organs, it provides protective padding. However, its main function is to be a reserve of lipids, which can be oxidised to meet the energy needs of the body and to protect it from excess glucose by storing triglycerides produced by the liver from sugars, although some evidence suggests that most lipid synthesis from carbohydrates occurs in the adipose tissue itself.JOURNAL, Aarsland A, Chinkes D, Wolfe RR, Hepatic and whole-body fat synthesis in humans during carbohydrate overfeeding, The American Journal of Clinical Nutrition, 65, 6, 1774–82, June 1997, 9174472,weblink 10.1093/ajcn/65.6.1774, Adipose depots in different parts of the body have different biochemical profiles. Under normal conditions, it provides feedback for hunger and diet to the brain.

Mice

File:Fatmouse.jpg|right|thumb|The obese mouse on the left has large stores of adipose tissue. It is unable to produce the hormone leptinleptinMice have eight major adipose depots, four of which are within the abdominal cavity. The paired gonadal depots are attached to the uterus and ovaries in females and the epididymis and testes in males; the paired retroperitoneal depots are found along the dorsal wall of the abdomen, surrounding the kidney, and, when massive, extend into the pelvis. The mesenteric depot forms a glue-like web that supports the intestines and the omental depot (which originates near the stomach and spleen) and - when massive - extends into the ventral abdomen. Both the mesenteric and omental depots incorporate much lymphoid tissue as lymph nodes and milky spots, respectively. The two superficial depots are the paired inguinal depots, which are found anterior to the upper segment of the hind limbs (underneath the skin) and the subscapular depots, paired medial mixtures of brown adipose tissue adjacent to regions of white adipose tissue, which are found under the skin between the dorsal crests of the scapulae. The layer of brown adipose tissue in this depot is often covered by a "frosting" of white adipose tissue; sometimes these two types of fat (brown and white) are hard to distinguish. The inguinal depots enclose the inguinal group of lymph nodes. Minor depots include the pericardial, which surrounds the heart, and the paired popliteal depots, between the major muscles behind the knees, each containing one large lymph node.BOOK, Pond, Caroline M., vanc, The Fats of Life, Cambridge University Press, 1998, 978-0-521-63577-6, Of all the depots in the mouse, the gonadal depots are the largest and the most easily dissected,JOURNAL, Cinti S, The adipose organ, Prostaglandins, Leukotrienes, and Essential Fatty Acids, 73, 1, 9–15, July 2005, 15936182, 10.1016/j.plefa.2005.04.010, comprising about 30% of dissectible fat.JOURNAL, Bachmanov AA, Reed DR, Tordoff MG, Price RA, Beauchamp GK, Nutrient preference and diet-induced adiposity in C57BL/6ByJ and 129P3/J mice, Physiology & Behavior, 72, 4, 603–13, March 2001, 11282146, 3341942, 10.1016/S0031-9384(01)00412-7, Alexander Bachmanov,

Obesity

In an obese person, excess adipose tissue hanging downward from the abdomen is referred to as a panniculus. A panniculus complicates surgery of the morbidly obese individual. It may remain as a literal "apron of skin" if a severely obese person quickly loses large amounts of fat (a common result of gastric bypass surgery). This condition cannot be effectively corrected through diet and exercise alone, as the panniculus consists of adipocytes and other supporting cell types shrunken to their minimum volume and diameter.{{citation needed|date=January 2011}} Reconstructive surgery is one method of treatment.{{citation needed|date=January 2017}}

Visceral fat{{Anchor|Abdominal fat}}

File:Abdominal obesity in men.jpg|thumb|240px|Abdominal obesityAbdominal obesity{{See also|Abdominal obesity}}Visceral fat or abdominal fatFat on the Inside: Looking Thin is Not Enough, By Fiona Haynes, About.com (also known as organ fat or intra-abdominal fat) is located inside the abdominal cavity, packed between the organs (stomach, liver, intestines, kidneys, etc.). Visceral fat is different from subcutaneous fat underneath the skin, and intramuscular fat interspersed in skeletal muscles. Fat in the lower body, as in thighs and buttocks, is subcutaneous and is not consistently spaced tissue, whereas fat in the abdomen is mostly visceral and semi-fluid.WEB,weblink Abdominal fat and what to do about it, September 2005, Visceral fat more of a health concern than subcutaneous fat, President & Fellows of Harvard College, Visceral fat is composed of several adipose depots, including mesenteric, epididymal white adipose tissue (EWAT), and perirenal depots. Visceral fat is often expressed in terms of its area in cm2 (VFA, visceral fat area).JOURNAL, Nagai M, Komiya H, Mori Y, Ohta T, Kasahara Y, Ikeda Y, Estimating visceral fat area by multifrequency bioelectrical impedance, Diabetes Care, 33, 5, 1077–79, May 2010, 20150289, 2858179, 10.2337/dc09-1099, An excess of visceral fat is known as central obesity, or "belly fat", in which the abdomen protrudes excessively. New developments such as the Body Volume Index (BVI) are specifically designed to measure abdominal volume and abdominal fat. Excess visceral fat is also linked to type 2 diabetes,JOURNAL, Montague CT, O'Rahilly S, The perils of portliness: causes and consequences of visceral adiposity, Diabetes, 49, 6, 883–88, June 2000, 10866038, 10.2337/diabetes.49.6.883, insulin resistance,JOURNAL, Kern PA, Ranganathan S, Li C, Wood L, Ranganathan G, Adipose tissue tumor necrosis factor and interleukin-6 expression in human obesity and insulin resistance, American Journal of Physiology. Endocrinology and Metabolism, 280, 5, E745–51, May 2001, 11287357, 10.1152/ajpendo.2001.280.5.e745, inflammatory diseases,JOURNAL, Marette A, Molecular mechanisms of inflammation in obesity-linked insulin resistance, International Journal of Obesity and Related Metabolic Disorders, 27 Suppl 3, S46–48, December 2003, 14704744, 10.1038/sj.ijo.0802500, and other obesity-related diseases.JOURNAL, Mokdad AH, Ford ES, Bowman BA, Dietz WH, Vinicor F, Bales VS, Marks JS, Prevalence of obesity, diabetes, and obesity-related health risk factors, 2001, JAMA, 289, 1, 76–79, January 2003, 12503980, 10.1001/jama.289.1.76, 6, Likewise, the accumulation of neck fat (or cervical adipose tissue) has been shown to be associated with mortality.JOURNAL, Maresky HS, Sharfman Z, Ziv-Baran T, Gomori JM, Copel L, Tal S, Anthropometric Assessment of Neck Adipose Tissue and Airway Volume Using Multidetector Computed Tomography: An Imaging Approach and Association With Overall Mortality, Medicine, 94, 45, e1991, November 2015, 26559286, 4912280, 10.1097/MD.0000000000001991, Several studies have suggested that visceral fat can be predicted from simple anthropometric measures,JOURNAL, Brown JC, Harhay MO, Harhay MN, Anthropometrically predicted visceral adipose tissue and blood-based biomarkers: a cross-sectional analysis, European Journal of Nutrition, 57, 1, 191–198, 2016, 27614626, 5513780, 10.1007/s00394-016-1308-8, and predicts mortality more accurately than body mass index or waist circumference.JOURNAL, Brown JC, Harhay MO, Harhay MN, Anthropometrically-predicted visceral adipose tissue and mortality among men and women in the third national health and nutrition examination survey (NHANES III), American Journal of Human Biology, 29, 1, e22898, 2017, 27427402, 5241265, 10.1002/ajhb.22898, Men are more likely to have fat stored in the abdomen due to sex hormone differences. Female sex hormone causes fat to be stored in the buttocks, thighs, and hips in women.WEB, Estrogen causes fat to be stored around the pelvic region, hips, butt and thighs (pelvic region), Reduce Abdominal Fat,weblink WEB,weblink Waistline Worries: Turning Apples Back Into Pears,weblink" title="web.archive.org/web/20090609161936weblink">weblink 2009-06-09, healthywomen.org, yes, When women reach menopause and the estrogen produced by the ovaries declines, fat migrates from the buttocks, hips and thighs to the waist;Researchers think that the lack of estrogen at menopause plays a role in driving our fat northward. See: WEB,weblink A Matter of Fat,weblink" title="web.archive.org/web/20070315044431weblink">weblink 2007-03-15, Andrews, Michelle, 2006-12-01, Yahoo Health, Women's Health, later fat is stored in the abdomen.High-intensity exercise is one way to effectively reduce total abdominal fat.JOURNAL, Irving BA, Davis CK, Brock DW, Weltman JY, Swift D, Barrett EJ, Gaesser GA, Weltman A, Effect of exercise training intensity on abdominal visceral fat and body composition, Medicine and Science in Sports and Exercise, 40, 11, 1863–72, November 2008, 18845966, 2730190, 10.1249/MSS.0b013e3181801d40, JOURNAL, Coker RH, Williams RH, Kortebein PM, Sullivan DH, Evans WJ, Influence of exercise intensity on abdominal fat and adiponectin in elderly adults, Metabolic Syndrome and Related Disorders, 7, 4, 363–68, August 2009, 19196080, 3135883, 10.1089/met.2008.0060, One study suggests at least 10 MET-hours per week of aerobic exercise is required for visceral fat reduction.JOURNAL, Ohkawara K, Tanaka S, Miyachi M, Ishikawa-Takata K, Tabata I, A dose-response relation between aerobic exercise and visceral fat reduction: systematic review of clinical trials, International Journal of Obesity, 31, 12, 1786–97, December 2007, 17637702, 10.1038/sj.ijo.0803683,

Epicardial fat

Epicardial adipose tissue (EAT) is a particular form of visceral fat deposited around the heart and found to be a metabolically active organ that generates various bioactive molecules, which might significantly affect cardiac function.JOURNAL, Mazurek T, Zhang L, Zalewski A, Mannion JD, Diehl JT, Arafat H, Sarov-Blat L, O'Brien S, Keiper EA, Johnson AG, Martin J, Goldstein BJ, Shi Y, Human epicardial adipose tissue is a source of inflammatory mediators, Circulation, 108, 20, 2460–66, November 2003, 14581396, 10.1161/01.CIR.0000099542.57313.C5, etal, Marked component differences have been observed in comparing EAT with subcutaneous fat, suggesting a depot specific impact of stored fatty acids on adipocyte function and metabolism.JOURNAL, Pezeshkian M, Noori M, Najjarpour-Jabbari H, Abolfathi A, Darabi M, Darabi M, Shaaker M, Shahmohammadi G, Fatty acid composition of epicardial and subcutaneous human adipose tissue, Metabolic Syndrome and Related Disorders, 7, 2, 125–31, April 2009, 19422139, 10.1089/met.2008.0056, etal,

Subcutaneous fat

{{See also|Body fat percentage}}(File:Blausen 0012 AdiposeTissue.png|thumb|Micro-anatomy of subcutaneous fat)Most of the remaining nonvisceral fat is found just below the skin in a region called the hypodermis.BOOK, Katja, Hoehn, Elaine N., Marieb, vanc, Anatomy & Physiology, 2008, Pearson/Benjamin Cummings, San Francisco, Calif., 978-0-8053-0094-9, 3rd, This subcutaneous fat is not related to many of the classic obesity-related pathologies, such as heart disease, cancer, and stroke, and some evidence even suggests it might be protective.JOURNAL, Porter SA, Massaro JM, Hoffmann U, Vasan RS, O'Donnel CJ, Fox CS, Abdominal subcutaneous adipose tissue: a protective fat depot?, Diabetes Care, 32, 6, 1068–75, June 2009, 19244087, 2681034, 10.2337/dc08-2280, The typically female (or gynecoid) pattern of body fat distribution around the hips, thighs, and buttocks is subcutaneous fat, and therefore poses less of a health risk compared to visceral fat.WEB,weblink Belly fat in women: Taking – and keeping – it off, MayoClinic.com, 2013-06-08, 2013-12-02, Like all other fat organs, subcutaneous fat is an active part of the endocrine system, secreting the hormones leptin and resistin.The relationship between the subcutaneous adipose layer and total body fat in a person is often modelled by using regression equations. The most popular of these equations was formed by Durnin and Wormersley, who rigorously tested many types of skinfold, and, as a result, created two formulae to calculate the body density of both men and women. These equations present an inverse correlation between skinfolds and body density—as the sum of skinfolds increases, the body density decreases.JOURNAL, Brodie D, Moscrip V, Hutcheon R, Body composition measurement: a review of hydrodensitometry, anthropometry, and impedance methods, Nutrition, 14, 3, 296–310, March 1998, 9583375, 10.1016/S0899-9007(97)00474-7, Factors such as sex, age, population size or other variables may make the equations invalid and unusable, and, {{As of|2012|lc=y}}, Durnin and Wormersley's equations remain only estimates of a person's true level of fatness. New formulae are still being created.

Marrow fat

Marrow fat, also known as marrow adipose tissue (MAT), is a poorly understood adipose depot that resides in the bone and is interspersed with hematopoietic cells as well as bony elements. The adipocytes in this depot are derived from mesenchymal stem cells (MSC) which can give rise to fat cells, bone cells as well as other cell types. The fact that MAT increases in the setting of calorie restriction/ anorexia is a feature that distinguishes this depot from other fat depots.JOURNAL, Devlin MJ, Cloutier AM, Thomas NA, Panus DA, Lotinun S, Pinz I, Baron R, Rosen CJ, Bouxsein ML, Caloric restriction leads to high marrow adiposity and low bone mass in growing mice, Journal of Bone and Mineral Research, 25, 9, 2078–88, September 2010, 20229598, 3127399, 10.1002/jbmr.82, JOURNAL, Cawthorn WP, Scheller EL, Parlee SD, Pham HA, Learman BS, Redshaw CM, Sulston RJ, Burr AA, Das AK, Simon BR, Mori H, Bree AJ, Schell B, Krishnan V, MacDougald OA, Expansion of Bone Marrow Adipose Tissue During Caloric Restriction Is Associated With Increased Circulating Glucocorticoids and Not With Hypoleptinemia, Endocrinology, 157, 2, 508–21, February 2016, 26696121, 4733126, 10.1210/en.2015-1477, JOURNAL, Bredella MA, Fazeli PK, Miller KK, Misra M, Torriani M, Thomas BJ, Ghomi RH, Rosen CJ, Klibanski A, Increased bone marrow fat in anorexia nervosa, The Journal of Clinical Endocrinology and Metabolism, 94, 6, 2129–36, June 2009, 19318450, 2690416, 10.1210/jc.2008-2532, Exercise regulates MAT, decreasing MAT quantity and diminishing the size of marrow adipocytes.JOURNAL, Styner M, Pagnotti GM, McGrath C, Wu X, Sen B, Uzer G, Xie Z, Zong X, Styner MA, Rubin CT, Rubin J, Exercise Decreases Marrow Adipose Tissue Through ß-Oxidation in Obese Running Mice, Journal of Bone and Mineral Research, 32, 8, 1692–702, August 2017, 28436105, 5550355, 10.1002/jbmr.3159, JOURNAL, Styner M, Pagnotti GM, Galior K, Wu X, Thompson WR, Uzer G, Sen B, Xie Z, Horowitz MC, Styner MA, Rubin C, Rubin J, Exercise Regulation of Marrow Fat in the Setting of PPARγ Agonist Treatment in Female C57BL/6 Mice, Endocrinology, 156, 8, 2753–61, August 2015, 26052898, 4511140, 10.1210/en.2015-1213, JOURNAL, Styner M, Thompson WR, Galior K, Uzer G, Wu X, Kadari S, Case N, Xie Z, Sen B, Romaine A, Pagnotti GM, Rubin CT, Styner MA, Horowitz MC, Rubin J, Bone marrow fat accumulation accelerated by high fat diet is suppressed by exercise, Bone, 64, 39–46, July 2014, 24709686, 4041820, 10.1016/j.bone.2014.03.044, The exercise regulation of marrow fat suggests that it bears some physiologic similarity to other white adipose depots. Moreover, increased MAT in obesity further suggests a similarity to white fat depots.

Ectopic fat

Ectopic fat is the storage of triglycerides in tissues other than adipose tissue, that are supposed to contain only small amounts of fat, such as the liver, skeletal muscle, heart, and pancreas. This can interfere with cellular functions and hence organ function and is associated with insulin resistance in type-2 diabetes.JOURNAL, Snel M, Jonker JT, Schoones J, Lamb H, de Roos A, Pijl H, Smit JW, Meinders AE, Jazet IM, Ectopic fat and insulin resistance: pathophysiology and effect of diet and lifestyle interventions, International Journal of Endocrinology, 2012, 1–18, 2012, 22675355, 3366269, 10.1155/2012/983814, It is stored in relatively high amounts around the organs of the abdominal cavity, but is not to be confused with visceral fat.The specific cause for the accumulation of ectopic fat is unknown. The cause is likely a combination of genetic, environmental, and behavioral factors that are involved in excess energy intake and decreased physical activity. Substantial weight loss can reduce ectopic fat stores in all organs and this is associated with an improvement of the function of that organ.In the latter case, non-invasive weight loss interventions like diet or exercise can decrease ectopic fat (particularly in heart and liver) in overweight or obese children and adults.JOURNAL, Hens W, Vissers D, Hansen D, Peeters S, Gielen J, Van Gaal L, Taeymans J, The effect of diet or exercise on ectopic adiposity in children and adolescents with obesity: a systematic review and meta-analysis, Obesity Reviews, 18, 11, 1310–22, 2017, 28913977, 10.1111/obr.12577, JOURNAL, Hens W, Taeyman J, Cornelis J, Gielen J, Van Gaal L, Vissers D, The Effect of Lifestyle Interventions on Excess Ectopic Fat Deposition Measured by Noninvasive Techniques in Overweight and Obese Adults: A Systematic Review and Meta-Analysis, Journal of Physical Activity & Health, 13, 6, 671–94, 2016, 26694194, 10.1123/jpah.2015-0560,

Physiology

Free fatty acids (FFAs) are liberated from lipoproteins by lipoprotein lipase (LPL) and enter the adipocyte, where they are reassembled into triglycerides by esterifying them onto glycerol. Human fat tissue contains about 87% lipids.{{Citation needed|date=April 2016}}There is a constant flux of FFAs entering and leaving adipose tissue. The net direction of this flux is controlled by insulin and leptin—if insulin is elevated, then there is a net inward flux of FFA, and only when insulin is low can FFA leave adipose tissue. Insulin secretion is stimulated by high blood sugar, which results from consuming carbohydrates.{{Citation needed|date=December 2017}}In humans, lipolysis (hydrolysis of triglycerides into free fatty acids) is controlled through the balanced control of lipolytic B-adrenergic receptors and a2A-adrenergic receptor-mediated antilipolysis.Fat cells have an important physiological role in maintaining triglyceride and free fatty acid levels, as well as determining insulin resistance. Abdominal fat has a different metabolic profile—being more prone to induce insulin resistance. This explains to a large degree why central obesity is a marker of impaired glucose tolerance and is an independent risk factor for cardiovascular disease (even in the absence of diabetes mellitus and hypertension).JOURNAL, Dhaliwal SS, Welborn TA, 2009, Central obesity and multivariable cardiovascular risk as assessed by the Framingham prediction scores, Am J Cardiol, 103, 10, 1403–07, 10.1016/j.amjcard.2008.12.048, 19427436, Studies of female monkeys at Wake Forest University (2009) discovered that individuals suffering from higher stress have higher levels of visceral fat in their bodies. This suggests a possible cause-and-effect link between the two, wherein stress promotes the accumulation of visceral fat, which in turn causes hormonal and metabolic changes that contribute to heart disease and other health problems.NEWS,weblinkweblink" title="archive.is/20131220014233weblink">weblink December 20, 2013, no, Fat-Bellied Monkeys Suggest Why Stress Sucks, Time magazine, Time, Alice, Park, vanc, 2009-08-08, 2013-12-19, Recent advances in biotechnology have allowed for the harvesting of adult stem cells from adipose tissue, allowing stimulation of tissue regrowth using a patient's own cells. In addition, adipose-derived stem cells from both human and animals reportedly can be efficiently reprogrammed into induced pluripotent stem cells without the need for feeder cells.JOURNAL, Sugii S, Kida Y, Kawamura T, Suzuki J, Vassena R, Yin YQ, Lutz MK, Berggren WT, Izpisúa Belmonte JC, Evans RM, Human and mouse adipose-derived cells support feeder-independent induction of pluripotent stem cells, Proceedings, 107, 8, 3558–63, February 2010, 20133714, 2840462, 10.1073/pnas.0910172106, 2010PNAS..107.3558S, 6, The use of a patient's own cells reduces the chance of tissue rejection and avoids ethical issues associated with the use of human embryonic stem cells.JOURNAL, Atzmon G, Yang XM, Muzumdar R, Ma XH, Gabriely I, Barzilai N, Differential gene expression between visceral and subcutaneous fat depots, Hormone and Metabolic Research = Hormon- und Stoffwechselforschung = Hormones et Metabolisme, 34, 11–12, 622–28, November 2002, 12660871, 10.1055/s-2002-38250, A growing body of evidence also suggests that different fat depots (i.e. abdominal, omental, pericardial) yield adipose-derived stem cells with different characteristics.JOURNAL, Baglioni S, Cantini G, Poli G, Francalanci M, Squecco R, Di Franco A, Borgogni E, Frontera S, Nesi G, Liotta F, Lucchese M, Perigli G, Francini F, Forti G, Serio M, Luconi M, Functional differences in visceral and subcutaneous fat pads originate from differences in the adipose stem cell, PLOS One, 7, 5, e36569, 4 May 2012, 22574183, 3344924, 10.1371/journal.pone.0036569, 2012PLoSO...736569B, These depot-dependent features include proliferation rate, immunophenotype, differentiation potential, gene expression, as well as sensitivity to hypoxic culture conditions.JOURNAL, Russo V, Yu C, Belliveau P, Hamilton A, Flynn LE, Comparison of human adipose-derived stem cells isolated from subcutaneous, omental, and intrathoracic adipose tissue depots for regenerative applications, Stem Cells Translational Medicine, 3, 2, 206–17, February 2014, 24361924, 3925056, 10.5966/sctm.2013-0125, Adipose tissue is the greatest peripheral source of aromatase in both males and females,{{Citation needed|date=July 2013}} contributing to the production of estradiol.Adipose derived hormones include: Adipose tissues also secrete a type of cytokines (cell-to-cell signalling proteins) called adipokines (adipose cytokines), which play a role in obesity-associated complications. Perivascular adipose tissue releases adipokines such as adiponectin that affect the contractile function of the vessels that they surround.JOURNAL, Löhn M, Dubrovska G, Lauterbach B, Luft FC, Gollasch M, Sharma AM, Periadventitial fat releases a vascular relaxing factor, FASEB Journal, 16, 9, 1057–63, July 2002, 12087067, 10.1096/fj.02-0024com,

Brown fat

Brown fat or brown adipose tissue (BAT) is a specialized form of adipose tissue important for adaptive thermogenesis in humans and other mammals. BAT can generate heat by "uncoupling" the respiratory chain of oxidative phosphorylation within mitochondria through tissue-specific expression of uncoupling protein 1 (UCP1). BAT is primarily located around the neck and large blood vessels of the thorax, where may effectively act in heat exchange. BAT is robustly activated upon cold exposure by the release of catecholamines from sympathetic nerves that results in UCP1 activation. BAT activation may also occur in response to overfeeding.JOURNAL, Busiello RA, Savarese S, Lombardi A, Mitochondrial uncoupling proteins and energy metabolism, Frontiers in Physiology, 6, 36, 36, 2015, 25713540, 4322621, 10.3389/fphys.2015.00036, UCP1 activity is stimulated by long chain fatty acids that are produced subsequent to β-adrenergic receptor activation.JOURNAL, Cannon B, Nedergaard J, Brown adipose tissue: function and physiological significance, Physiological Reviews, 84, 1, 277–359, January 2004, 14715917, 10.1152/physrev.00015.2003, UCP1 is proposed to function as a fatty acid proton symporter, although the exact mechanism has yet to be elucidated.JOURNAL, Fedorenko A, Lishko PV, Kirichok Y, Mechanism of fatty-acid-dependent UCP1 uncoupling in brown fat mitochondria, Cell, 151, 2, 400–13, October 2012, 23063128, 3782081, 10.1016/j.cell.2012.09.010, In contrast, UCP1 is inhibited by ATP, ADP, and GTP.JOURNAL, Azzu V, Brand MD, The on-off switches of the mitochondrial uncoupling proteins, Trends in Biochemical Sciences, 35, 5, 298–307, May 2010, 20006514, 3640847, 10.1016/j.tibs.2009.11.001, Attempts to simulate this process pharmacologically have so far been unsuccessful. Techniques to manipulate the differentiation of "brown fat" could become a mechanism for weight loss therapy in the future, encouraging the growth of tissue with this specialized metabolism without inducing it in other organs.Until recently, brown adipose tissue was thought to be primarily limited to infants in humans, but new evidence has now overturned that belief. Metabolically active tissue with temperature responses similar to brown adipose was first reported in the neck and trunk of some human adults in 2007,JOURNAL, Nedergaard J, Bengtsson T, Cannon B, Unexpected evidence for active brown adipose tissue in adult humans, American Journal of Physiology. Endocrinology and Metabolism, 293, 2, E444–52, August 2007, 17473055, 10.1152/ajpendo.00691.2006, and the presence of brown adipose in human adults was later verified histologically in the same anatomical regions.JOURNAL, Virtanen KA, Lidell ME, Orava J, Heglind M, Westergren R, Niemi T, Taittonen M, Laine J, Savisto NJ, Enerbäck S, Nuutila P, Functional brown adipose tissue in healthy adults, The New England Journal of Medicine, 360, 15, 1518–25, April 2009, 19357407, 10.1056/NEJMoa0808949, 6, JOURNAL, van Marken Lichtenbelt WD, Vanhommerig JW, Smulders NM, Drossaerts JM, Kemerink GJ, Bouvy ND, Schrauwen P, Teule GJ, Cold-activated brown adipose tissue in healthy men, The New England Journal of Medicine, 360, 15, 1500–08, April 2009, 19357405, 10.1056/NEJMoa0808718, 6, JOURNAL, Cypess AM, Lehman S, Williams G, Tal I, Rodman D, Goldfine AB, Kuo FC, Palmer EL, Tseng YH, Doria A, Kolodny GM, Kahn CR, Identification and importance of brown adipose tissue in adult humans, The New England Journal of Medicine, 360, 15, 1509–17, April 2009, 19357406, 2859951, 10.1056/NEJMoa0810780, 6,

Beige fat and WAT browning

(File:Adipocyte types.jpg|right|thumb|Morphology of three different classes of adipocytes)Browning of WAT, also referred to as "beiging", occurs when adipocytes within WAT depots develop features of BAT. Beige adipocytes take on a multilocular appearance (containing several lipid droplets) and increase expression of uncoupling protein 1 (UCP1).JOURNAL, Harms M, Seale P, Brown and beige fat: development, function and therapeutic potential, Nature Medicine, 19, 10, 1252–63, October 2013, 24100998, 10.1038/nm.3361, In doing so, these normally energy-storing adipocytes become energy-releasing adipocytes.The calorie-burning capacity of brown and beige fat has been extensively studied as research efforts focus on therapies targeted to treat obesity and diabetes. The drug 2,4-dinitrophenol, which also acts as a chemical uncoupler similarly to UCP1, was used for weight loss in the 1930s. However, it was quickly discontinued when excessive dosing led to adverse side effects including hyperthermia and death. β3 agonists, like CL316,243, have also been developed and tested in humans. However, the use of such drugs has proven largely unsuccessful due to several challenges, including varying species receptor specificity and poor oral bioavailability.JOURNAL, Cypess AM, Kahn CR, Brown fat as a therapy for obesity and diabetes, Current Opinion in Endocrinology, Diabetes and Obesity, 17, 2, 143–49, April 2010, 20160646, 3593105, 10.1097/MED.0b013e328337a81f, Cold is a primary regulator of BAT processes and induces WAT browning. Browning in response to chronic cold exposure has been well documented and is a reversible process. A study in mice demonstrated that cold-induced browning can be completely reversed in 21 days, with measurable decreases in UCP1 seen within a 24-hour period.JOURNAL, Gospodarska E, Nowialis P, Kozak LP, Mitochondrial turnover: a phenotype distinguishing brown adipocytes from interscapular brown adipose tissue and white adipose tissue, The Journal of Biological Chemistry, 290, 13, 8243–55, March 2015, 25645913, 4375480, 10.1074/jbc.M115.637785, A study by Rosenwald et al. revealed that when the animals are re-exposed to a cold environment, the same adipocytes will adopt a beige phenotype, suggesting that beige adipocytes are retained.JOURNAL, Rosenwald M, Perdikari A, Rülicke T, Wolfrum C, Bi-directional interconversion of brite and white adipocytes, Nature Cell Biology, 15, 6, 659–67, June 2013, 23624403, 10.1038/ncb2740, Transcriptional regulators, as well as a growing number of other factors, regulate the induction of beige fat. Four regulators of transcription are central to WAT browning and serve as targets for many of the molecules known to influence this process.JOURNAL, Lo KA, Sun L, Turning WAT into BAT: a review on regulators controlling the browning of white adipocytes, Bioscience Reports, 33, 5, 711–19, September 2013, 23895241, 3764508, 10.1042/BSR20130046, These include peroxisome proliferator-activated receptor gamma (PPARγ), PR domain containing 16 (PRDM16),JOURNAL, Harms MJ, Ishibashi J, Wang W, Lim HW, Goyama S, Sato T, Kurokawa M, Won KJ, Seale P, Prdm16 is required for the maintenance of brown adipocyte identity and function in adult mice, Cell Metabolism, 19, 4, 593–604, April 2014, 24703692, 4012340, 10.1016/j.cmet.2014.03.007, peroxisome proliferator-activated receptor gamma coactivator 1 alpha (PGC-1α), and Early B-Cell Factor-2 (EBF2).JOURNAL, Wang W, Kissig M, Rajakumari S, Huang L, Lim HW, Won KJ, Seale P, Ebf2 is a selective marker of brown and beige adipogenic precursor cells, Proceedings, 111, 40, 14466–71, October 2014, 25197048, 4209986, 10.1073/pnas.1412685111, 2014PNAS..11114466W, JOURNAL, Kissig M, Shapira SN, Seale P, SnapShot: Brown and Beige Adipose Thermogenesis, Cell, 166, 1, 258–258.e1, June 2016, 27368105, 5478388, 10.1016/j.cell.2016.06.038, JOURNAL, Shapira SN, Lim HW, Rajakumari S, Sakers AP, Ishibashi J, Harms MJ, Won KJ, Seale P, EBF2 transcriptionally regulates brown adipogenesis via the histone reader DPF3 and the BAF chromatin remodeling complex, Genes & Development, 31, 7, 660–73, April 2017, 28428261, 5411707, 10.1101/gad.294405.116, The list of molecules that influence browning has grown in direct proportion to the popularity of this topic and is constantly evolving as more knowledge is acquired. Among these molecules are irisin and fibroblast growth factor 21 (FGF21), which have been well-studied and are believed to be important regulators of browning. Irisin is secreted from muscle in response to exercise and has been shown to increase browning by acting on beige preadipocytes.JOURNAL, Boström P, Wu J, Jedrychowski MP, Korde A, Ye L, Lo JC, Rasbach KA, Boström EA, Choi JH, Long JZ, Kajimura S, Zingaretti MC, Vind BF, Tu H, Cinti S, Højlund K, Gygi SP, Spiegelman BM, A PGC1-α-dependent myokine that drives brown-fat-like development of white fat and thermogenesis, Nature, 481, 7382, 463–68, January 2012, 22237023, 3522098, 10.1038/nature10777, 2012Natur.481..463B, FGF21, a hormone secreted mainly by the liver, has garnered a great deal of interest after being identified as a potent stimulator of glucose uptake and a browning regulator through its effects on PGC-1α. It is increased in BAT during cold exposure and is thought to aid in resistance to diet-induced obesityJOURNAL, Ohta H, Itoh N, Roles of FGFs as Adipokines in Adipose Tissue Development, Remodeling, and Metabolism, Frontiers in Endocrinology, 5, 18, 18, 2014, 24605108, 3932445, 10.3389/fendo.2014.00018, FGF21 may also be secreted in response to exercise and a low protein diet, although the latter has not been thoroughly investigated.JOURNAL, Fenzl A, Kiefer FW, Brown adipose tissue and thermogenesis, Hormone Molecular Biology and Clinical Investigation, 19, 1, 25–37, July 2014, 25390014, 10.1515/hmbci-2014-0022, JOURNAL, Laeger T, Henagan TM, Albarado DC, Leanne Redman, Redman LM, Bray GA, Noland RC, Münzberg H, Hutson SM, Gettys TW, Schwartz MW, Morrison CD, FGF21 is an endocrine signal of protein restriction, The Journal of Clinical Investigation, 124, 9, 3913–22, September 2014, 25133427, 4153701, 10.1172/JCI74915, Data from these studies suggest that environmental factors like diet and exercise may be important mediators of browning. In mice, it was found that beiging can occur through the production of methionine-enkephalin peptides by type 2 innate lymphoid cells in response to interleukin 33.JOURNAL, Brestoff, Jonathan R., Kim, Brian S., Saenz, Steven A., Stine, Rachel R., Monticelli, Laurel A., Sonnenberg, Gregory F., Thome, Joseph J., Farber, Donna L., Lutfy, Kabirullah, 12 March 2015, Group 2 innate lymphoid cells promote beiging of white adipose tissue and limit obesity, Nature, En, 519, 7542, 242–246, 10.1038/nature14115, 25533952, 1476-4687, 4447235, 2015Natur.519..242B,

Genomics and bioinformatics tools to study browning

Due to the complex nature of adipose tissue and a growing list of browning regulatory molecules, great potential exists for the use of bioinformatics tools to improve study within this field. Studies of WAT browning have greatly benefited from advances in these techniques, as beige fat is rapidly gaining popularity as a therapeutic target for the treatment of obesity and diabetes.DNA microarray is a bioinformatics tool used to quantify expression levels of various genes simultaneously, and has been used extensively in the study of adipose tissue. One such study used microarray analysis in conjunction with Ingenuity IPA software to look at changes in WAT and BAT gene expression when mice were exposed to temperatures of 28 and 6 Â°C.JOURNAL, Rosell M, Kaforou M, Frontini A, Okolo A, Chan YW, Nikolopoulou E, Millership S, Fenech ME, MacIntyre D, Turner JO, Moore JD, Blackburn E, Gullick WJ, Cinti S, Montana G, Parker MG, Christian M, Brown and white adipose tissues: intrinsic differences in gene expression and response to cold exposure in mice, American Journal of Physiology. Endocrinology and Metabolism, 306, 8, E945–64, April 2014, 24549398, 3989735, 10.1152/ajpendo.00473.2013, The most significantly up- and downregulated genes were then identified and used for analysis of differentially expressed pathways. It was discovered that many of the pathways upregulated in WAT after cold exposure are also highly expressed in BAT, such as oxidative phosphorylation, fatty acid metabolism, and pyruvate metabolism. This suggests that some of the adipocytes switched to a beige phenotype at 6 Â°C. Mössenböck et al. also used microarray analysis to demonstrate that insulin deficiency inhibits the differentiation of beige adipocytes but does not disturb their capacity for browning.JOURNAL, Inagaki T, Sakai J, Kajimura S, Transcriptional and epigenetic control of brown and beige adipose cell fate and function, Nature Reviews Molecular Cell Biology, 17, 8, 480–95, August 2016, 27251423, 4956538, 10.1038/nrm.2016.62, These two studies demonstrate the potential for the use of microarray in the study of WAT browning.RNA sequencing (RNA-Seq) is a powerful computational tool that allows for the quantification of RNA expression for all genes within a sample. Incorporating RNA-Seq into browning studies is of great value, as it offers better specificity, sensitivity, and a more comprehensive overview of gene expression than other methods. RNA-Seq has been used in both human and mouse studies in an attempt characterize beige adipocytes according to their gene expression profiles and to identify potential therapeutic molecules that may induce the beige phenotype. One such study used RNA-Seq to compare gene expression profiles of WAT from wild-type (WT) mice and those overexpressing Early B-Cell Factor-2 (EBF2). WAT from the transgenic animals exhibited a brown fat gene program and had decreased WAT specific gene expression compared to the WT mice.JOURNAL, Stine RR, Shapira SN, Lim HW, Ishibashi J, Harms M, Won KJ, Seale P, EBF2 promotes the recruitment of beige adipocytes in white adipose tissue, Molecular Metabolism, 5, 1, 57–65, January 2016, 26844207, 4703852, 10.1016/j.molmet.2015.11.001, Thus, EBF2 has been identified as a potential therapeutic molecule to induce beiging.Chromatin immunoprecipitation with sequencing (ChIP-seq) is a method used to identify protein binding sites on DNA and assess histone modifications. This tool has enabled examination of epigenetic regulation of browning and helps elucidate the mechanisms by which protein-DNA interactions stimulate the differentiation of beige adipocytes. Studies observing the chromatin landscapes of beige adipocytes have found that adipogenesis of these cells results from the formation of cell specific chromatin landscapes, which regulate the transcriptional program and, ultimately, control differentiation. Using ChIP-seq in conjunction with other tools, recent studies have identified over 30 transcriptional and epigenetic factors that influence beige adipocyte development.

Genetics

The thrifty gene hypothesis (also called the famine hypothesis) states that in some populations the body would be more efficient at retaining fat in times of plenty, thereby endowing greater resistance to starvation in times of food scarcity. This hypothesis, originally advanced in the context of glucose metabolism and insulin resistance, has been discredited by physical anthropologists, physiologists, and the original proponent of the idea himself with respect to that context, although according to its developer it remains "as viable as when [it was] first advanced" in other contexts.BOOK, Speakerman, John R., vanc, Genetics of Obesity: Five Fundamental Problems with the Famine Hypothesis, Fantuzzi G, Mazzone T, Adipose Tissue and Adipokines in Health and Disease, 221–236, Humana Press, 2007, 10.1007/978-1-59745-370-7_17, 978-1-58829-721-1, Nutrition and Health, JOURNAL, Neel JV, The study of natural selection in primitive and civilized human populations. 1958, Human Biology, 61, 5–6, 781–810; discussion 811–23, 1989, 2699601, In 1995, Jeffrey Friedman, in his residency at the Rockefeller University, together with Rudolph Leibel, Douglas Coleman et al. discovered the protein leptin that the genetically obese mouse lacked.BOOK, Shell E, The Hungry Gene: The Inside Story of the Obesity Industry, Atlantic Monthly Press, January 1, 2002, Chapter 4: On the Cutting Edge, 978-1-4223-5243-4, JOURNAL, Pelleymounter MA, Cullen MJ, Baker MB, Hecht R, Winters D, Boone T, Collins F, Effects of the obese gene product on body weight regulation in ob/ob mice, Science, 269, 5223, 540–43, July 1995, 7624776, 10.1126/science.7624776, 1995Sci...269..540P, 6, Leptin is produced in the white adipose tissue and signals to the hypothalamus. When leptin levels drop, the body interprets this as a loss of energy, and hunger increases. Mice lacking this protein eat until they are four times their normal size.Leptin, however, plays a different role in diet-induced obesity in rodents and humans. Because adipocytes produce leptin, leptin levels are elevated in the obese. However, hunger remains, and—when leptin levels drop due to weight loss—hunger increases. The drop of leptin is better viewed as a starvation signal than the rise of leptin as a satiety signal.BOOK, Eric, Ravussin, Steven R., Smith, vanc, Chapter 11: Role of the Adipocyte in Metabolism and Endocrine Function, Gordon C, Weir, J. Larry, Jameson, Leslie J., De Groot, Endocrinology Adult and Pediatric, Diabetes Mellitus and Obesity, 2013, 6th, 978-0-323-22154-2, Elsevier Health Sciences, {{page needed|date=May 2012}} However, elevated leptin in obesity is known as leptin resistance. The changes that occur in the hypothalamus to result in leptin resistance in obesity are currently the focus of obesity research.JOURNAL, Morris DL, Rui L, Recent advances in understanding leptin signaling and leptin resistance, American Journal of Physiology. Endocrinology and Metabolism, 297, 6, E1247–59, December 2009, 19724019, 2793049, 10.1152/ajpendo.00274.2009, Gene defects in the leptin gene (ob) are rare in human obesity.JOURNAL, Carlsson B, Lindell K, Gabrielsson B, Karlsson C, Bjarnason R, Westphal O, Karlsson U, Sjöström L, Carlsson LM, Obese (ob) gene defects are rare in human obesity, Obesity Research, 5, 1, 30–35, January 1997, 9061713, 10.1002/j.1550-8528.1997.tb00280.x, 6, {{as of|2010|July|}}, only 14 individuals from five families have been identified worldwide who carry a mutated ob gene (one of which was the first ever identified cause of genetic obesity in humans)—two families of Pakistani origin living in the UK, one family living in Turkey, one in Egypt, and one in AustriaJOURNAL, Montague CT, Farooqi IS, Whitehead JP, Soos MA, Rau H, Wareham NJ, Sewter CP, Digby JE, Mohammed SN, Hurst JA, Cheetham CH, Earley AR, Barnett AH, Prins JB, O'Rahilly S, Congenital leptin deficiency is associated with severe early-onset obesity in humans, Nature, 387, 6636, 903–8, June 1997, 9202122, 10.1038/43185, 1997Natur.387..903M, JOURNAL, Strobel A, Issad T, Camoin L, Ozata M, Strosberg AD, A leptin missense mutation associated with hypogonadism and morbid obesity, Nature Genetics, 18, 3, 213–15, March 1998, 9500540, 10.1038/ng0398-213, JOURNAL, Gibson WT, Farooqi IS, Moreau M, DePaoli AM, Lawrence E, O'Rahilly S, Trussell RA, Congenital leptin deficiency due to homozygosity for the Delta133G mutation: report of another case and evaluation of response to four years of leptin therapy, The Journal of Clinical Endocrinology and Metabolism, 89, 10, 4821–26, October 2004, 15472169, 10.1210/jc.2004-0376, JOURNAL, Mazen I, El-Gammal M, Abdel-Hamid M, Amr K, A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient, Molecular Genetics and Metabolism, 97, 4, 305–08, August 2009, 19427251, 10.1016/j.ymgme.2009.04.002, JOURNAL, Fischer-Posovszky P, von Schnurbein J, Moepps B, Lahr G, Strauss G, Barth TF, Kassubek J, Mühleder H, Möller P, Debatin KM, Gierschik P, Wabitsch M, A new missense mutation in the leptin gene causes mild obesity and hypogonadism without affecting T cell responsiveness, The Journal of Clinical Endocrinology and Metabolism, 95, 6, 2836–40, June 2010, 20382689, 10.1210/jc.2009-2466, —and two other families have been found that carry a mutated ob receptor.JOURNAL, Clément K, Vaisse C, Lahlou N, Cabrol S, Pelloux V, Cassuto D, Gourmelen M, Dina C, Chambaz J, Lacorte JM, Basdevant A, Bougnères P, Lebouc Y, Froguel P, Guy-Grand B, A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction, Nature, 392, 6674, 398–401, 1998, 9537324, 10.1038/32911, 1998Natur.392..398C, JOURNAL, Pankov YA, Adipose tissue as an endocrine organ regulating growth, puberty, and other physiological functions, Biochemistry. Biokhimiia, 64, 6, 601–09, 1999, 10395972, Others have been identified as genetically partially deficient in leptin, and, in these individuals, leptin levels on the low end of the normal range can predict obesity.JOURNAL, Farooqi IS, Keogh JM, Kamath S, Jones S, Gibson WT, Trussell R, Jebb SA, Lip GY, O'Rahilly S, Partial leptin deficiency and human adiposity, Nature, 414, 6859, 34–35, November 2001, 11689931, 10.1038/35102112, 2001Natur.414...34F, Several mutations of genes involving the melanocortins (used in brain signaling associated with appetite) and their receptors have also been identified as causing obesity in a larger portion of the population than leptin mutations.JOURNAL, Farooqi IS, O'Rahilly S, Mutations in ligands and receptors of the leptin-melanocortin pathway that lead to obesity, Nature Clinical Practice Endocrinology & Metabolism, 4, 10, 569–77, October 2008, 18779842, 10.1038/ncpendmet0966,

Physical properties

Adipose tissue has a density of ~0.9 g/ml.JOURNAL, Farvid MS, Ng TW, Chan DC, Barrett PH, Watts GF, Association of adiponectin and resistin with adipose tissue compartments, insulin resistance and dyslipidaemia, Diabetes, Obesity & Metabolism, 7, 4, 406–13, July 2005, 15955127, 10.1111/j.1463-1326.2004.00410.x, {{Registration required}} Thus, a person with more adipose tissue will float more easily than a person of the same weight with more muscular tissue, since muscular tissue has a density of 1.06 g/ml.JOURNAL, Urbanchek MG, Picken EB, Kalliainen LK, Kuzon WM, Specific force deficit in skeletal muscles of old rats is partially explained by the existence of denervated muscle fibers, The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 56, 5, B191–97, May 2001, 11320099, 10.1093/gerona/56.5.B191,weblink

Body fat meter

{{See also|Bioelectrical impedance analysis}}A body fat meter is a widely available tool used to measure the percentage of fat in the human body. Different meters use various methods to determine the body fat to weight ratio. They tend to under-read body fat percentage.In contrast with clinical tools, one relatively inexpensive type of body fat meter uses the principle of bioelectrical impedance analysis (BIA) in order to determine an individual's body fat percentage. To achieve this, the meter passes a small, harmless, electric current through the body and measures the resistance, then uses information on the person's weight, height, age, and sex to calculate an approximate value for the person's body fat percentage. The calculation measures the total volume of water in the body (lean tissue and muscle contain a higher percentage of water than fat), and estimates the percentage of fat based on this information. The result can fluctuate several percentage points depending on what has been eaten and how much water has been drunk before the analysis. Before bioelectrical impedance analysis machines were developed, there were many different ways in analyzing body composition such as skin fold methods using calipers, underwater weighing, whole body air displacement plethysmography (ADP) and DXA.

Animal studies

Within the fat (adipose) tissue of CCR2 deficient mice, there is an increased number of eosinophils, greater alternative Macrophage activation, and a propensity towards type 2 cytokine expression. Furthermore, this effect was exaggerated when the mice became obese from a high fat diet.JOURNAL, Bolus WR, Gutierrez DA, Kennedy AJ, Anderson-Baucum EK, Hasty AH, CCR2 deficiency leads to increased eosinophils, alternative macrophage activation, and type 2 cytokine expression in adipose tissue, Journal of Leukocyte Biology, 98, 4, 467–77, October 2015, 25934927, 4763864, 10.1189/jlb.3HI0115-018R,weblink 2016-09-08,weblink" title="web.archive.org/web/20170509015901weblink">weblink 2017-05-09, yes,

Gallery

Image:Gray940.png|Diagrammatic sectional view of the skin (magnified).
Image:Yellow adipose tissue in paraffin section - lipids washed out.jpg|White adipose tissue in paraffin section
Image:Body Fat meter.jpg|Electronic instrument of body fat meter

See also

References

{{Reflist}}

Further reading

  • {{MeshNumber|A10.165.114|Adipose+tissue}}
  • ENCYCLOPEDIA, Stock, M. J., Cinti, S., vanc, Encyclopedia of Food Sciences and Nutrition, 29–34, 2003, 10.1016/B0-12-227055-X/00008-0, Adipose Tissue / Structure and Function of Brown Adipose Tissue, 978-0-12-227055-0,
  • ENCYCLOPEDIA, Vernon, R. G., Flint, D. J., vanc, Encyclopedia of Food Sciences and Nutrition, 23–29, 2003, 10.1016/B0-12-227055-X/00007-9, Adipose Tissue / Structure and Function of White Adipose Tissue, 978-0-12-227055-0,

External links

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