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Bone marrow adipose tissue

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Switzerland in 2017 (BMA2017). The statues were then signed at the fourth international meeting, held in 2018 again in Lille (BMA2018). As discussed in the following section, there have since been three further international meetings, held in Odense, Denmark in 2019 (BMA2019), virtually in 2020 (BMA2020), and in Athens, Greece in 2022 (BMA2022). The first BMAS Summer School was held virtually in the summer of 2021.
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meeting was a great success and led to a second international meeting (BMA2016) in August 2016 held in Rotterdam, The Netherlands. Both meetings were a success in that they for the first time brought together scientists and physicians from different backgrounds (bone metabolism, cancer, obesity and diabetes) to share ideas and advance research into, and our understanding of, the patho/physiological role of BMAds.
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This success led to a network of researchers discussing the formation of a new society, focusing on bone marrow adiposity (BMA). This network worked together in 2016–2017 to lay the foundations for this society, which was then discussed further during the third international meeting held in Lausanne,
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Because of the increasing interest in BMAT from both researchers and clinicians, in 2018 The International Bone Marrow Adiposity Society (BMAS) was founded. Work to build the society began in Lille, France in 2015, when the first International Meeting on Bone Marrow Adiposity (BMA2015) was held. The
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This figure demonstrates the use of the osmium- μCT method with advanced image processing to quantify BMAT. In this figure, running exercise is shown to suppress BMAT despite PPARγ agonist. Fat binder osmium is imaged via μCT (A ) in n =5 per group overlaid images. Quantification of osmium as BMAT/
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of osmium-bound lipid volume (in mm) relative to bone volume. This technique provides reproducible quantification and visualization of BMAT, enabling the ability to consistently quantify changes in BMAT with diet, exercise, and agents that constrain precursor lineage allocation. Although the osmium
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Several studies have also analysed BMAT function in vivo using positron emission tomography - computed tomography (PET-CT) combined with the tracer 18F-Fluorodeoxyglucose (FDG). This allows glucose uptake, a measure of metabolic activity, to be quantified in living organisms, including humans. Two
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therapies. BMAT decreases in anaemia, leukaemia, and hypertensive heart failure; in response to hormones such as oestrogen, leptin, and growth hormone; with exercise-induced weight loss or bariatric surgery; in response to chronic cold exposure; and in response to pharmacological agents such as
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This figure demonstrates the use of MRI imaging (9.4T scanner) along with advanced image processing to quantify BMAT. The images and graph demonstrate that BMAT is higher in obese compared with lean mice. B6 mice were fed HFD from age 4 wk until age 16 wk. BMAT was quantified by MRI. A) n=10
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quantification can be used to purify adipocytes from the stromal vascular fraction of most fat depots. Early research with such machinery cited adipocytes as too large and fragile for cytometer-based purification, rendering them susceptible to lysis; however, recent advances have been made to
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was published in 2014; Now, exercise regulation of BMAT has been confirmed in a human, adding clinical importance. Several studies demonstrated exercise reduction of BMAT which occurs along with an increase in bone quantity. Since exercise increases bone quantity, reduces BMAT and increases
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have published three position papers relating to nomenclature, methodologies and biobanking for BMA research. These working groups remain active, with other working groups also focussing on clinical and translational issues, public engagement, and young researchers (Next Generation BMAS)
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method is quantitatively precise, osmium is toxic and cannot be compared across batched experiments. Recently, researchers developed and validated a 9.4T MRI scanner technique that allows localization and volumetric (3D) quantification that can be compared across experiments, as in.
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recent studies found that, unlike brown adipose tissue, BMAT does not increase glucose uptake in response to cold exposure, demonstrating that BMAT is functionally distinct from BAT. The full extent of BMAT's impact on systemic metabolic homeostasis remains to be determined.
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Rosen CJ, Ackert-Bicknell CL, Adamo ML, Shultz KL, Rubin J, Donahue LR, et al. (November 2004). "Congenic mice with low serum IGF-I have increased body fat, reduced bone mineral density, and an altered osteoblast differentiation program".
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and cannot adequately quantify the volume of fat in the marrow. Nevertheless, histological techniques and fixation make possible visualization of BMAT, quantification of BMAd size, and BMAT's association with the surrounding
3785:"Reporting Guidelines, Review of Methodological Standards, and Challenges Toward Harmonization in Bone Marrow Adiposity Research. Report of the Methodologies Working Group of the International Bone Marrow Adiposity Society" 3664:
Scheller EL, Troiano N, Vanhoutan JN, Bouxsein MA, Fretz JA, Xi Y, et al. (2014). "Use of Osmium Tetroxide Staining with Microcomputerized Tomography to Visualize and Quantify Bone Marrow Adipose Tissue in Vivo".
277:+ marrow MSC is separated from non-bone fat storage by larger expression of bone transcription factors", and likely indicates a different fat phenotype. Recently, BMAT was noted to "produce a greater proportion of 257:(VAT) is a distinct type of WAT that is "proportionally associated with negative metabolic and cardiovascular morbidity", regenerates cortisol, and recently has been tied to decreased bone formation Both types of 321:
also decrease BMAT while increasing bone density, supporting an inverse relationship between bone quantity and BMAT. During aging, bone quantity declines and fat redistributes from subcutaneous to
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Meunier P, Aaron J, Edouard C, Vignon G (October 1971). "Osteoporosis and the replacement of cell populations of the marrow by adipose tissue. A quantitative study of 84 iliac bone biopsies".
205:. A notable exception occurs in the setting of caloric restriction: exercise suppression of BMAT does not yield an increase in bone formation and even appears to cause bone loss. Indeed, 2866:"Aging activates adipogenic and suppresses osteogenic programs in mesenchymal marrow stroma/stem cells: the role of PPAR-gamma2 transcription factor and TGF-beta/BMP signaling pathways" 1040:"Standardised Nomenclature, Abbreviations, and Units for the Study of Bone Marrow Adiposity: Report of the Nomenclature Working Group of the International Bone Marrow Adiposity Society" 4178: 387:
In order to understand the physiology of BMAT, various analytic methods have been applied. BMAds are difficult to isolate and quantify because they are interspersed with bony and
4205: 3286:"Mechanical loading down-regulates peroxisome proliferator-activated receptor gamma in bone marrow stromal cells and favors osteoblastogenesis at the expense of adipogenesis" 527:
Representative distal femur histologic section of a 16-week-old C57BL/6 mouse after 6 weeks of calorie restriction demonstrating an increased quantity of marrow adipocytes.
3836:"Guidelines for Biobanking of Bone Marrow Adipose Tissue and Related Cell Types: Report of the Biobanking Working Group of the International Bone Marrow Adiposity Society" 3885:
Hardouin P, Marie PJ, Rosen CJ (December 2016). "New insights into bone marrow adipocytes: Report from the First European Meeting on Bone Marrow Adiposity (BMA 2015)".
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expression or decreased Wnt10b. Thus, bone fragility, osteoporosis, and osteoporotic fractures are thought to be linked to mechanisms which promote BMAT accumulation.
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based on the inverse relationship between bone and BMAT in bone-fragile osteoporotic states. An increase in BMAT is noted in osteoporosis clinical studies measured by
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is associated with lower osteogenic and greater adipogenic biasing of MSC. This aging-related biasing of MSC away from osteoblast lineage may represent higher basal
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Masuzaki H, Paterson J, Shinyama H, Morton NM, Mullins JJ, Seckl JR, Flier JS (December 2001). "A transgenic model of visceral obesity and the metabolic syndrome".
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fat. However, more-recent functional and -omics studies have shown that BMAT is a unique adipose depot that is molecularly and functionally distinct to WAT or BAT.
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BMAT increases in states of bone fragility. BMAT is thought to result from preferential MSC differentiation into an adipocyte, rather than osteoblast lineage in
171:, rather than osteoblast, lineage in the setting of osteoporosis. Since BMAT is increased in the setting of obesity and is suppressed by endurance exercise, or 2588:"Quantification of vertebral bone marrow fat content using 3 Tesla MR spectroscopy: reproducibility, vertebral variation, and applications in osteoporosis" 2355:"Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential" 439:-based marrow density measurements. A volumetric method to identify, quantify, and localize BMAT in rodent bone has been recently developed, requiring 953:"Effects of rosiglitazone vs metformin on circulating osteoclast and osteogenic precursor cells in postmenopausal women with type 2 diabetes mellitus" 302: 334: 2257:"Abdominal fat is associated with lower bone formation and inferior bone quality in healthy premenopausal women: a transiliac bone biopsy study" 478:
bone volume in the whole femur is shown. a, significant due to Rosi. b, significant due to exercise. Rosi=rosiglizaone, CTL=control, E=exercise.
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Recent advances in cell surface and intracellular marker identification and single-cell analyses led to greater resolution and high-throughput
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Representative distal femur histologic section of a 16-week-old healthy C57BL/6 mouse demonstrating a typical quantity of marrow adipocytes.
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mitigate this; nevertheless, this methodology continues to pose technical challenges and is inaccessible to much of the research community.
363:, a microenvironment that contains cells and secreted factors that promote appropriate renewal and differentiation of HSC. The study of the 4182: 3374:
Majka SM, Miller HL, Helm KM, Acosta AS, Childs CR, Kong R, Klemm DJ (2014). "Analysis and Isolation of Adipocytes by Flow Cytometry".
1512:"Mechanical Signals As a Non-Invasive Means to Influence Mesenchymal Stem Cell Fate, Promoting Bone and Suppressing the Fat Phenotype" 2539:"Osteoporosis is associated with increased marrow fat content and decreased marrow fat unsaturation: a proton MR spectroscopy study" 2447:"Bone marrow adipose tissue is an endocrine organ that contributes to increased circulating adiponectin during caloric restriction" 84: 1299:"A High Fat Diet Increases Bone Marrow Adipose Tissue (MAT) But Does Not Alter Trabecular or Cortical Bone Mass in C57BL/6J Mice" 424: 306: 132: 2494:
Duque G, Li W, Adams M, Xu S, Phipps R (May 2011). "Effects of risedronate on bone marrow adipocytes in postmenopausal women".
3103:"Short-term exposure to low-carbohydrate, high-fat diets induces low bone mineral density and reduces bone formation in rats" 1011: 869:"Transforming growth factor beta2 inhibits adipocyte differentiation induced by skeletal unloading in rat bone marrow stroma" 17: 2686:"Effects of sex and age on bone microstructure at the ultradistal radius: a population-based noninvasive in vivo assessment" 351:
cells (also known as blood cells) reside in the bone marrow along with BMAds. These hematopoietic cells are derived from
3468:"Vertebral bone marrow fat is positively associated with visceral fat and inversely associated with IGF-1 in obese women" 197:
expression of markers of fatty acid oxidation in bone, BMAT is thought to be providing needed fuel for exercise-induced
2915:"Wnt10b deficiency results in age-dependent loss of bone mass and progressive reduction of mesenchymal progenitor cells" 1091:"Adipocyte differentiation of bone marrow-derived mesenchymal stem cells: cross talk with the osteoblastogenic program" 3682: 3391: 2112:
Wronska A, Kmiec Z (June 2012). "Structural and biochemical characteristics of various white adipose tissue depots".
355:(HSC) which give rise to diverse cells: cells of the blood, immune system, as well as cells that break down bone ( 2069:
Tilg H, Moschen AR (October 2006). "Adipocytokines: mediators linking adipose tissue, inflammation and immunity".
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has been used with success to quantify vertebral BMAT in humans, it is difficult to employ in laboratory animals.
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Tchkonia T, Morbeck DE, Von Zglinicki T, Van Deursen J, Lustgarten J, Scrable H, et al. (October 2010).
1617:"Exercise and Diet: Uncovering Prospective Mediators of Skeletal Fragility in Bone and Marrow Adipose Tissue" 209:
availability appears to be a factor in the ability of exercise to regulate BMAT. Another exception occurs in
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Wronski TJ, Morey ER (1982-01-01). "Skeletal abnormalities in rats induced by simulated weightlessness".
376: 310: 238: 1758:"Bone marrow fat has brown adipose tissue characteristics, which are attenuated with aging and diabetes" 1297:
Doucette CR, Horowitz MC, Berry R, MacDougald OA, Anunciado-Koza R, Koza RA, Rosen CJ (September 2015).
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has published hundreds of presentations and articles on BMAT featured in the ASBMR annual meetings, The
175:, it is likely that BMAT physiology, in the setting of mechanical input/exercise, approximates that of 762:
Fazeli PK, Horowitz MC, MacDougald OA, Scheller EL, Rodeheffer MS, Rosen CJ, Klibanski A (March 2013).
658: 428: 3517:"VDR haploinsufficiency impacts body composition and skeletal acquisition in a gender-specific manner" 1867:"Bone marrow adipose tissue does not express UCP1 during development or adrenergic-induced remodeling" 3718:"Human Bone Marrow Adipose Tissue is a Metabolically Active and Insulin-Sensitive Distinct Fat Depot" 3564:
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Rubin MR, Manavalan JS, Agarwal S, McMahon DJ, Nino A, Fitzpatrick LA, Bilezikian JP (October 2014).
1353:"Exercise Regulation of Marrow Fat in the Setting of PPARγ Agonist Treatment in Female C57BL/6 Mice" 3834:
Lucas S, Tencerova M, von der Weid B, Andersen TL, Attané C, Behler-Janbeck F, et al. (2021).
3566:"Marrow fat and preadipocyte factor-1 levels decrease with recovery in women with anorexia nervosa" 3054:"Bone marrow adipocytes promote the regeneration of stem cells and haematopoiesis by secreting SCF" 1810:"Bone marrow adipose tissue is a unique adipose subtype with distinct roles in glucose homeostasis" 820:"Exercise Degrades Bone in Caloric Restriction, Despite Suppression of Marrow Adipose Tissue (MAT)" 3325:
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1924:"Bone marrow adipocytes resist lipolysis and remodeling in response to β-adrenergic stimulation" 1705:
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1248:"Changes in Skeletal Integrity and Marrow Adiposity during High-Fat Diet and after Weight Loss" 67: 4122:
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444: 436: 164: 153: 2637:"Effects of estrogen therapy on bone marrow adipocytes in postmenopausal osteoporotic women" 1971:
Attané C, Estève D, Chaoui K, Iacovoni JS, Corre J, Moutahir M, et al. (January 2020).
1666:"Energy Deficiency Suppresses Bone Turnover in Exercising Women With Menstrual Disturbances" 1151:"The Role of Bone Marrow Fat in Skeletal Health: Usefulness and Perspectives for Clinicians" 678:
Cohen A, Dempster DW, Stein EM, Nickolas TL, Zhou H, McMahon DJ, et al. (August 2012).
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superimposed group average images are shown B) BMAT normalized to bone volume in each group.
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Tratwal J, Labella R, Bravenboer N, Kerckhofs G, Douni E, Scheller EL, et al. (2020).
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contain excess energy, indicating a clear evolutionary advantage during times of scarcity.
234: 230: 176: 3615:"Differential effects of exercise on tibial shaft marrow density in young female athletes" 3142:
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1707:"Exercise Increases Bone in SEIPIN Deficient Lipodystrophy, Despite Low Marrow Adiposity" 124: 3244: 2735:"Age-related changes in trabecular architecture differ in female and male C57BL/6J mice" 2168: 1882: 1825: 1115: 1090: 1038:
Bravenboer N, Bredella MA, Chauveau C, Corsi A, Douni E, Ferris WF, et al. (2020).
4232: 4150: 4123: 4099: 4072: 4048: 4021: 3997: 3970: 3946: 3921: 3862: 3835: 3811: 3784: 3742: 3717: 3693: 3674: 3590: 3565: 3541: 3516: 3492: 3467: 3402: 3383: 3351: 3326: 3261: 3228: 3168: 3144:"Sclerostin antibody inhibits skeletal deterioration due to reduced mechanical loading" 3143: 3078: 3053: 3029: 3004: 2939: 2914: 2890: 2865: 2800: 2775: 2710: 2685: 2661: 2636: 2612: 2587: 2568: 2519: 2471: 2446: 2427: 2379: 2354: 2330: 2305: 2281: 2256: 2255:
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1223: 1198: 1128: 1066: 1039: 1017: 1003: 898: 844: 819: 788: 763: 704: 679: 372: 254: 3229:"Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment" 1463:"Combating osteoporosis and obesity with exercise: leveraging cell mechanosensitivity" 1461:
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285:", suggesting an endocrine function for this depot, akin, but different, from that of 4247: 4155: 4104: 4053: 4002: 3971:"Brief Report From the 3rd International Meeting on Bone Marrow Adiposity (BMA 2017)" 3951: 3902: 3867: 3816: 3747: 3698: 3678: 3646: 3641: 3595: 3546: 3497: 3448: 3407: 3387: 3356: 3307: 3266: 3209: 3173: 3124: 3083: 3034: 2985: 2962:
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1411:"Exercise Decreases Marrow Adipose Tissue Through ß-Oxidation in Obese Running Mice" 902: 88:
Bone marrow adipocytes are derived from mesenchymal stem cell (MSC) differentiation.
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techniques have been developed as a means to visualize and quantify BMAT. Although
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Styner M, Thompson WR, Galior K, Uzer G, Wu X, Kadari S, et al. (July 2014).
163:, among other cell types. Thus, it is thought that BMAT results from preferential 2037: 1989: 1972: 420: 364: 360: 318: 274: 156: 1756:
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2462: 2208:"Determinants of bone microarchitecture and mechanical properties in obese men" 1939: 1890: 1833: 1773: 1632: 1214: 885: 868: 625: 448: 412: 396: 391:
elements. Until recently, qualitative measurements of BMAT have relied on bone
214: 128: 108: 4140: 4089: 4073:"Report From the 6th International Meeting on Bone Marrow Adiposity (BMA2020)" 3852: 3532: 3052:
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Methods for Quantification of Bone Marrow Adipose Tissue (BMAT)
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BMAds secrete factors that promote HSC renewal in most bones.
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The first study to demonstrate exercise regulation of BMAT in
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950: 3465: 3324: 3226: 1558: 3922:"Meeting report of the 2016 bone marrow adiposity meeting" 3765: 3424: 1970: 1803: 1801: 866: 677: 340: 281:– an adipokine associated with improved metabolism – than 3669:. Methods in Enzymology. Vol. 537. pp. 123–39. 3378:. Methods in Enzymology. Vol. 537. pp. 281–96. 1148: 726: 249:
and inflammatory markers which have both positive (e.g.,
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Scheller EL, McGee-Lawrence ME, Lecka-Czernik B (2021).
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Logo for The International Bone Marrow Adiposity Society
2536: 2401: 2205: 1864: 1798: 1460: 1408: 1245: 115:. It increases in states of low bone density, such as 4019: 1350: 1088: 540:
The International Bone Marrow Adiposity Society (BMAS)
224: 4181:. University of Michigan. 3 July 2014. Archived from 3373: 379:, there is interest in improving the renewal of HSC. 3722:
The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
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The Journal of Clinical Endocrinology and Metabolism
2961: 1755: 1509: 1089:Muruganandan S, Roman AA, Sinal CJ (January 2009). 3884: 3002: 2585: 643:features many presentations and articles on BMAT. 3766:"The International Bone Marrow Adiposity Society" 2303: 992:Cawthorn W (2020). "Bone Marrow Adipose Tissue". 273:location, and its adipocyte origin from at least 229:BMAT has been reported to have qualities of both 4214: 998:. Oxford, UK: Academic Press. pp. 156–177. 3920:van der Eerden B, van Wijnen A (October 2017). 3427:"Flow cytometric analysis of mature adipocytes" 425:proton magnetic resonance spectroscopy (1H-MRS) 2493: 2304:Wu J, Cohen P, Spiegelman BM (February 2013). 606:American Society for Bone and Mineral Research 140:bisphosphonates, teriparatide, and metformin. 3051: 918:Metabolic Bone Disease & Related Research 2776:"Fat tissue, aging, and cellular senescence" 2111: 915: 313:reduces BMAT. Antiresorptive therapies like 221:is possible, even with minimal BMAT stores. 2822: 2068: 729:Clinical Orthopaedics and Related Research 265:as by a group of proteins that help BAT's 4208:. Society for Endocrinology. Winter 2017. 4149: 4139: 4098: 4088: 4047: 4037: 4020:Penel G, Kerckhofs G, Chauveau C (2019). 3996: 3986: 3945: 3861: 3851: 3810: 3800: 3741: 3692: 3667:Methods of Adipose Tissue Biology, Part A 3640: 3630: 3589: 3540: 3491: 3442: 3401: 3376:Methods of Adipose Tissue Biology, Part A 3350: 3301: 3260: 3167: 3118: 3077: 3028: 2979: 2938: 2889: 2840: 2799: 2750: 2709: 2660: 2611: 2554: 2470: 2378: 2329: 2280: 2231: 2045: 2019: 1988: 1947: 1898: 1841: 1781: 1732: 1722: 1681: 1640: 1586: 1576: 1535: 1486: 1434: 1376: 1322: 1273: 1263: 1222: 1166: 1114: 1065: 1055: 968: 884: 843: 787: 703: 419:To improve quantification of BMAT, novel 404:, milieu of cells, and secreted factors. 375:. As such cancers are often treated with 371:in order to improve therapy for multiple 991: 547: 292: 83: 764:"Marrow fat and bone--new perspectives" 534: 341:Maintenance of hematopoietic stem cells 14: 4215: 187: 2592:Journal of Magnetic Resonance Imaging 2543:Journal of Magnetic Resonance Imaging 1610: 1608: 1606: 1456: 1454: 1404: 1402: 1400: 1398: 1396: 1346: 1344: 1342: 1192: 1190: 1188: 1186: 3570:Journal of Bone and Mineral Research 3148:Journal of Bone and Mineral Research 3107:Journal of Bone and Mineral Research 2968:Journal of Bone and Mineral Research 2919:Journal of Bone and Mineral Research 2739:Journal of Bone and Mineral Research 2690:Journal of Bone and Mineral Research 1565:Journal of Bone and Mineral Research 1415:Journal of Bone and Mineral Research 1095:Cellular and Molecular Life Sciences 873:Journal of Bone and Mineral Research 824:Journal of Bone and Mineral Research 813: 811: 809: 807: 635: 616:Journal of Bone and Mineral Research 359:). HSC renewal occurs in the marrow 225:Relationships to other types of fat 213:, a condition with reduced overall 24: 4170: 3675:10.1016/b978-0-12-411619-1.00007-0 3384:10.1016/b978-0-12-411619-1.00015-x 1603: 1451: 1393: 1339: 1183: 1004:10.1016/B978-0-12-801238-3.11207-3 25: 4259: 2823:Kassem M, Marie PJ (April 2011). 804: 2882:10.1111/j.1474-9728.2004.00127.x 2842:10.1111/j.1474-9726.2011.00669.x 2792:10.1111/j.1474-9726.2010.00608.x 2404:Journal of Cellular Biochemistry 2126:10.1111/j.1748-1716.2012.02409.x 741:10.1097/00003086-197110000-00021 657: This article incorporates 652: 595:BMA Summer School 2021 (virtual) 577:BMA2016 (Rotterdam, Netherlands) 568: 518: 502: 485: 468: 431:provides BMAT assessment in the 429:Magnetic resonance imaging (MRI) 4115: 4064: 4013: 3962: 3913: 3878: 3827: 3776: 3758: 3709: 3657: 3606: 3557: 3508: 3459: 3418: 3367: 3318: 3277: 3220: 3184: 3135: 3094: 3045: 2996: 2955: 2906: 2857: 2816: 2767: 2726: 2677: 2628: 2579: 2530: 2487: 2438: 2395: 2346: 2297: 2248: 2199: 2148: 2105: 2062: 2020:Ye R, Scherer PE (April 2013). 2013: 1964: 1915: 1858: 1749: 1698: 1657: 1552: 1503: 1290: 1239: 1082: 580:BMA2017 (Lausanne, Switzerland) 3521:Calcified Tissue International 3009:Cell Death and Differentiation 1303:Journal of Cellular Physiology 985: 944: 909: 860: 755: 720: 671: 447:imaging, followed by advanced 382: 45:Musculoskeletal (or locomotor) 13: 1: 3938:10.1080/21623945.2017.1313374 2359:Stem Cell Reviews and Reports 1467:Nature Reviews. Endocrinology 646: 592:BMA2020 (virtual BMA meeting) 269:role. BMAT, by its "specific 182: 131:such as that which occurs in 2038:10.1016/j.molmet.2013.04.001 1990:10.1016/j.celrep.2019.12.089 1621:Current Osteoporosis Reports 995:Encyclopedia of Bone Biology 930:10.1016/0221-8747(82)90011-X 367:is relevant to the field of 99:), sometimes referred to as 7: 395:, which is subject to site 377:bone marrow transplantation 311:postmenopausal osteoporosis 154:mesenchymal stem cell (MSC) 10: 4264: 4128:Frontiers in Endocrinology 4077:Frontiers in Endocrinology 4026:Frontiers in Endocrinology 3975:Frontiers in Endocrinology 3899:10.1016/j.bone.2015.11.013 3840:Frontiers in Endocrinology 3789:Frontiers in Endocrinology 3206:10.1016/j.bone.2004.07.008 2641:Osteoporosis International 2496:Osteoporosis International 2463:10.1016/j.cmet.2014.06.003 2071:Nature Reviews. Immunology 1940:10.1016/j.bone.2018.01.016 1891:10.1038/s41598-019-54036-x 1834:10.1038/s41467-020-16878-2 1774:10.1016/j.bone.2011.06.016 1711:Frontiers in Endocrinology 1633:10.1007/s11914-020-00634-y 1252:Frontiers in Endocrinology 1215:10.1016/j.bone.2014.03.044 1044:Frontiers in Endocrinology 886:10.1359/jbmr.2002.17.4.668 263:brown adipose tissue (BAT) 261:substantially differ from 217:stores: exercise- induced 143: 93:Bone marrow adipose tissue 30:Bone marrow adipose tissue 4141:10.3389/fendo.2022.879588 4090:10.3389/fendo.2021.712088 3853:10.3389/fendo.2021.744527 3533:10.1007/s00223-011-9505-1 2653:10.1007/s00198-008-0574-6 2508:10.1007/s00198-010-1353-8 2371:10.1007/s12015-012-9365-8 1724:10.3389/fendo.2021.782194 1479:10.1038/s41574-019-0170-1 1107:10.1007/s00018-008-8429-z 167:differentiation into the 66: 54: 49: 39: 34: 29: 4039:10.3389/fendo.2019.00691 3988:10.3389/fendo.2019.00336 3802:10.3389/fendo.2020.00065 1265:10.3389/fendo.2016.00102 1057:10.3389/fendo.2019.00923 353:hematopoietic stem cells 2310:Genes & Development 2177:10.1126/science.1066285 583:BMA2018 (Lille, France) 574:BMA2015 (Lille, France) 159:that also give rise to 152:(BMAds) originate from 4243:Musculoskeletal system 3734:10.1210/clinem/dgaa216 3444:10.1002/cyto.990100416 2322:10.1101/gad.211649.112 560:Since its foundation, 553: 443:staining of bones and 255:Visceral abdominal fat 245:is also the source of 239:Subcutaneous white fat 89: 68:Anatomical terminology 61:adipose ossium medulla 3642:10536/DRO/DU:30060423 1814:Nature Communications 1683:10.1210/jc.2019-00089 1588:10536/DRO/DU:30106029 551: 329:, muscle, and liver. 293:Impact on bone health 101:marrow adipose tissue 87: 18:Marrow adipose tissue 3632:10.1210/jc.2012-3748 3484:10.1038/oby.2010.106 3303:10.1210/en.2006-1704 3021:10.1038/cdd.2015.168 2273:10.1210/jc.2013-1047 2224:10.1210/jc.2012-2246 2026:Molecular Metabolism 1369:10.1210/en.2015-1213 1168:10.1210/jc.2015-2338 970:10.1210/jc.2013-3666 780:10.1210/jc.2012-3634 696:10.1210/jc.2012-1477 535:Scientific societies 435:in conjunction with 177:white adipose tissue 3253:10.1038/nature08099 3245:2009Natur.460..259N 3120:10.1359/jbmr.090813 3058:Nature Cell Biology 2981:10.1359/jbmr.070810 2752:10.1359/jbmr.070507 2702:10.1359/jbmr.050916 2169:2001Sci...294.2166M 2163:(5549): 2166–2170. 1883:2019NatSR...917427C 1826:2020NatCo..11.3097S 1516:BoneKEy Osteovision 963:(10): E1933–E1942. 562:BMAS working groups 373:hematologic cancers 188:Exercise regulation 125:caloric restriction 3343:10.4161/adip.21496 2604:10.1002/jmri.22489 2556:10.1002/jmri.20367 1871:Scientific Reports 554: 433:vertebral skeleton 90: 4185:on 15 March 2015. 3582:10.1002/jbmr.1640 3239:(7252): 259–263. 3160:10.1002/jbmr.1807 2974:(12): 1924–1932. 2925:(10): 2138–2147. 2416:10.1002/jcb.20777 2218:(11): 4115–4122. 2114:Acta Physiologica 1983:(4): 949–958.e6. 1578:10.1002/jbmr.3357 1427:10.1002/jbmr.3159 1315:10.1002/jcp.24954 1161:(10): 3613–3621. 1013:978-0-12-814082-6 836:10.1002/jbmr.3872 641:Endocrine society 636:Endocrine Society 589:(Odense, Denmark) 82: 81: 77: 16:(Redirected from 4255: 4209: 4198: 4186: 4164: 4163: 4153: 4143: 4119: 4113: 4112: 4102: 4092: 4068: 4062: 4061: 4051: 4041: 4017: 4011: 4010: 4000: 3990: 3966: 3960: 3959: 3949: 3917: 3911: 3910: 3882: 3876: 3875: 3865: 3855: 3831: 3825: 3824: 3814: 3804: 3780: 3774: 3773: 3762: 3756: 3755: 3745: 3728:(7): 2300–2310. 3713: 3707: 3706: 3696: 3661: 3655: 3654: 3644: 3634: 3625:(5): 2037–2044. 3610: 3604: 3603: 3593: 3576:(9): 1864–1871. 3561: 3555: 3554: 3544: 3512: 3506: 3505: 3495: 3463: 3457: 3456: 3446: 3422: 3416: 3415: 3405: 3371: 3365: 3364: 3354: 3322: 3316: 3315: 3305: 3296:(5): 2553–2562. 3281: 3275: 3274: 3264: 3224: 3218: 3217: 3200:(5): 1046–1058. 3188: 3182: 3181: 3171: 3139: 3133: 3132: 3122: 3098: 3092: 3091: 3081: 3049: 3043: 3042: 3032: 3015:(7): 1128–1139. 3000: 2994: 2993: 2983: 2959: 2953: 2952: 2942: 2931:10.1002/jbmr.118 2910: 2904: 2903: 2893: 2861: 2855: 2854: 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Index

Marrow adipose tissue
System
Latin
Anatomical terminology
edit on Wikidata

fat deposit
bone marrow
osteoporosis
anorexia nervosa
caloric restriction
unweighting
space travel
diabetes
adipocytes
mesenchymal stem cell (MSC)
progenitors
osteoblasts
MSC
adipocyte
vibration
white adipose tissue
rodents
bone formation
anabolism
energy
lipodystrophy
adipose
anabolism
white

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