Corrigendum: Region-specific variation in the properties of skeletal adipocytes reveals regulated and constitutive marrow adipose tissues (Nature Communications (2015) 6 (7808) DOI: 10.1038/ncomms8808);Region-specific variation in the properties of skeletal adipocytes reveals regulated and constitutive marrow adipose tissues

Nature Communications

Volumn 6, Issue , 2015, Pages

  Scheller, Erica L ^a,f   Doucette, Casey R ^b   Learman, Brian S ^a   Cawthorn, William P ^a   Khandaker, Shaima ^a   Schell, Benjamin ^a   Wu, Brent ^a   Ding, Shi Ying ^c   Bredella, Miriam A ^d   Fazeli, Pouneh K ^d   Khoury, Basma ^e   Jepsen, Karl J ^e   Pilch, Paul F ^c   Klibanski, Anne ^d   Rosen, Clifford J ^b   MacDougald, Ormond A ^a  

^a UNIVERSITY OF MICHIGAN   (United States)

^b Maine Medical Center Research Institute   (United States)

^c BOSTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d MASSACHUSETTS GENERAL HOSPITAL   (United States)

^e UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^f WASHINGTON UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CAVEOLIN; CAVEOLIN 1; CCAAT ENHANCER BINDING PROTEIN BETA; CCAAT ENHANCER BINDING PROTEIN DELTA; MONOUNSATURATED FATTY ACID; PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR GAMMA; STEROL REGULATORY ELEMENT BINDING PROTEIN 1; TRANSCRIPTION FACTOR; FATTY ACID; MEMBRANE PROTEIN; PTRF PROTEIN, MOUSE; RNA BINDING PROTEIN;

ABNORMALITY; CELLS AND CELL COMPONENTS; FAT; FATTY ACID; GENE EXPRESSION; HOMINID; METABOLISM; RODENT; SKELETON;

ADIPOCYTE; ADIPOGENESIS; ADIPOSE TISSUE; ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BONE MARROW; CELL MATURATION; CELL SIZE; CELL SUBPOPULATION; COLD EXPOSURE; CONGENITAL GENERALIZED LIPODYSTROPHY; CONGENITAL GENERALIZED LIPODYSTROPHY TYPE 4; CONTROLLED STUDY; CYTOGENETICS; FATTY ACID DESATURATION; GENE EXPRESSION; HEMATOPOIESIS; HUMAN; HUMAN CELL; LIPID COMPOSITION; LIPIDOMICS; MALE; MARROW ADIPOSE TISSUE; MOUSE; NONHUMAN; POSTNATAL DEVELOPMENT; RAT; REGULATORY MECHANISM; SKELETAL ADIPOCYTE; ANIMAL; BONE MARROW CELL; C3H MOUSE; C57BL MOUSE; COLD; CYTOLOGY; FEMALE; GROWTH, DEVELOPMENT AND AGING; KNOCKOUT MOUSE; LIPID METABOLISM; METABOLISM; PHYSIOLOGY; PROTON NUCLEAR MAGNETIC RESONANCE; SPRAGUE DAWLEY RAT;

MUS; RATTUS;

ADIPOCYTES; ANIMALS; BONE MARROW; BONE MARROW CELLS; COLD TEMPERATURE; FATTY ACIDS; FEMALE; HUMANS; LIPID METABOLISM; MALE; MEMBRANE PROTEINS; MICE, INBRED C3H; MICE, INBRED C57BL; MICE, KNOCKOUT; PROTON MAGNETIC RESONANCE SPECTROSCOPY; RATS, SPRAGUE-DAWLEY; RNA-BINDING PROTEINS; TRANSCRIPTION FACTORS;

EID: 84938831380     PISSN: None     EISSN: 20411723     Source Type: Journal    
DOI: 10.1038/ncomms13775     Document Type: Erratum

References (48)

1. Cawthorn, W. P. et al. Bone marrow adipose tissue is an endocrine organ that contributes to increased circulating adiponectin during caloric restriction. Cell Metab. 20, 368-375 (2014).
2. Scheller, E. L. & Rosen, C. J. What's the matter with MAT? Marrow adipose tissue, metabolism, and skeletal health. Ann. N Y Acad. Sci. 1311, 14-30 (2014).
3. Fazeli, P. K. et al. Marrow fat and bone-new perspectives. J. Clin. Endocrinol. Metab. 98, 935-945 (2013).
4. Motyl, K. J. & McCabe, L. R. Leptin treatment prevents type I diabetic marrow adiposity but not bone loss in mice. J. Cell. Physiol. 218, 376-384 (2009).
5. Botolin, S. & McCabe, L. R. Inhibition of PPARgamma prevents type I diabetic bone marrow adiposity but not bone loss. J. Cell. Physiol. 209, 967-976 (2006).
6. Iwaniec, U. T. & Turner, R. T. Failure to generate bone marrow adipocytes does not protect mice from ovariectomy-induced osteopenia. Bone 53, 145-153 (2013).
7. Miyakoshi, N. et al. Histomorphometric evaluation of the effects of ovariectomy on bone turnover in rat caudal vertebrae. Calcif. Tissue Int. 64, 318-324 (1999).
8. Li, M., Shen, Y., Qi, H. & Wronski, T. J. Comparative study of skeletal response to estrogen depletion at red and yellow marrow sites in rats. Anat. Record 245, 472-480 (1996).
9. Ma, Y. F., Ke, H. Z. & Jee, W. S. Prostaglandin E2 adds bone to a cancellous bone site with a closed growth plate and low bone turnover in ovariectomized rats. Bone 15, 137-146 (1994).
10. Naveiras, O. et al. Bone-marrow adipocytes as negative regulators of the haematopoietic microenvironment. Nature 460, 259-263 (2009).
11. Tavassoli, M. Marrow adipose cells. Histochemical identification of labile and stable components. Arch. Pathol. Lab. Med. 100, 16-18 (1976).
12. Emery, J. L. & Follett, G. F. Regression of bone-marrow haemopoiesis from the terminal digits in the foetus and infant. Br. J. Haematol. 10, 485-489 (1964).
13. Kricun, M. E. Red-yellow marrow conversion: its effect on the location of some solitary bone lesions. Skeletal Radiol. 14, 10-19 (1985).
14. Buie, H. R., Moore, C. P. & Boyd, S. K. Postpubertal architectural developmental patterns differ between the L3 vertebra and proximal tibia in three inbred strains of mice. J. Bone Miner. Res. 23, 2048-2059 (2008).
15. Cinti, S. The adipose organ. Prostaglandins Leukot. Essent. Fatty Acids 73, 9-15 (2005).
16. Khoury, B. M. et al. The use of nano-computed tomography to enhance musculoskeletal research. Connect. Tissue Res. 56, 106-119 (2015).
17. Scheller, E. L. et al. Use of osmium tetroxide staining with microcomputerized tomography to visualize and quantify bone marrow adipose tissue in vivo. Methods Enzymol. 537, 123-139 (2014).
18. Bredella, M. A. et al. Marrow fat composition in anorexia nervosa. Bone 66, 199-204 (2014).
19. Rodbell, M. Metabolism of isolated fat cells. I. Effects of hormones on glucose metabolism and lipolysis. J. Biol. Chem. 239, 375-380 (1964).
20. Hussain, S. O., Barbato, J. C., Koch, L. G., Metting, P. J. & Britton, S. L. Cardiac function in rats selectively bred for low-And high-capacity running. Am. J. Physiol. Regul. Integr. Comp. Physiol. 281, R1787-R1791 (2001).
21. Xia, J., Mandal, R., Sinelnikov, Broadhurst, D. & Wishart, D. S. MetaboAnalyst 2.0-A comprehensive server for metabolomic data analysis. Nucleic Acids Res. 40, W127-W133 (2012).
22. Rosen, E. D. & MacDougald, O. A. Adipocyte differentiation from the inside out. Nat. Rev. Mol. Cell Biol. 7, 885-896 (2006).
23. Cao, Z., Umek, R. M. & McKnight, S. L. Regulated expression of three C/EBP isoforms during adipose conversion of 3T3-L1 cells. Genes Dev. 5, 1538-1552 (1991).
24. Thorn, H. et al. Cell surface orifices of caveolae and localization of caveolin to the necks of caveolae in adipocytes. Mol. Biol. Cell 14, 3967-3976 (2003).
25. Hayashi, Y. K. et al. Human PTRF mutations cause secondary deficiency of caveolins resulting in muscular dystrophy with generalized lipodystrophy. J. Clin. Invest. 119, 2623-2633 (2009).
26. Liu, L. et al. Deletion of Cavin/PTRF causes global loss of caveolae, dyslipidemia, and glucose intolerance. Cell Metab. 8, 310-317 (2008).
27. Liu, L. & Pilch, P. F. A critical role of cavin (polymerase I and transcript release factor) in caveolae formation and organization. J. Biol. Chem. 283, 4314-4322 (2008).
28. Hill, M. M. et al. PTRF-Cavin, a conserved cytoplasmic protein required for caveola formation and function. Cell 132, 113-124 (2008).
29. Parker, V. E., Savage, D. B., O'Rahilly, S. & Semple, R. K. Mechanistic insights into insulin resistance in the genetic era. Diabet. Med. 28, 1476-1486 (2011).
30. Baker, N., Zhang, G., You, Y. & Tuan, R. S. Caveolin-1 regulates proliferation and osteogenic differentiation of human mesenchymal stem cells. J. Cell. Biochem. 113, 3773-3787 (2012).
31. Razani, B. et al. Caveolin-1-deficient mice are lean, resistant to diet-induced obesity, and show hypertriglyceridemia with adipocyte abnormalities. J. Biol. Chem. 277, 8635-8647 (2002).
32. Ding, S. Y. et al. Pleiotropic effects of cavin-1 deficiency on lipid metabolism. J. Biol. Chem. 289, 8473-8483 (2014).
33. Asterholm, I. W., Mundy, D. I., Weng, J., Anderson, R. G. & Scherer, P. E. Altered mitochondrial function and metabolic inflexibility associated with loss of caveolin-1. Cell Metab. 15, 171-185 (2012).
34. Kim, C. A. et al. Association of a homozygous nonsense caveolin-1 mutation with Berardinelli-Seip congenital lipodystrophy. J. Clin. Endocrinol. Metab. 93, 1129-1134 (2008).
35. Tavassoli, M., Watson, L. R. & Khademi, R. Retention of hemopoiesis in tail vertebrae of newborn rats. Cell Tissue Res. 200, 215-222 (1979).
36. Bigelow, C. L. & Tavassoli, M. Fatty involution of bone marrow in rabbits. Acta Anat. (Basel) 118, 60-64 (1984).
37. Elleder, M. & Lojda, Z. Studies in lipid histochemistry. I. Criticism of performic and peracetic acid-schiff reactions. Histochemie 24, 7-20 (1970).
38. Yeung, D. K. et al. Osteoporosis is associated with increased marrow fat content and decreased marrow fat unsaturation: a proton MR spectroscopy study. J. Magn. Reson. Imaging 22, 279-285 (2005).
39. Patsch, J. M. et al. Bone marrow fat composition as a novel imaging biomarker in postmenopausal women with prevalent fragility fractures. J. Bone Miner. Res. 28, 1721-1728 (2013).
40. Gunaratnam, K., Vidal, C., Gimble, J. M. & Duque, G. Mechanisms of palmitate-induced lipotoxicity in human osteoblasts. Endocrinology 155, 108-116 (2014).
41. Cao, H. et al. Identification of a lipokine, a lipid hormone linking adipose tissue to systemic metabolism. Cell 134, 933-944 (2008).
42. Nelson-Dooley, C., Della-Fera, M. A., Hamrick, M. & Baile, C. A. Novel treatments for obesity and osteoporosis: targeting apoptotic pathways in adipocytes. Curr. Med. Chem. 12, 2215-2225 (2005).
43. Schneider, C. A., Rasband, W. S. & Eliceiri, K. W. NIH Image to ImageJ: 25 years of image analysis. Nat. Methods 9, 671-675 (2012).
44. Parlee, S. D., Lentz, S. I., Mori, H. & MacDougald, O. A. Quantifying size and number of adipocytes in adipose tissue. Methods Enzymol. 537, 93-122 (2014).
45. Bligh, E. G. & Dyer, W. J. A rapid method of total lipid extraction and purification. Can. J. Biochem. Physiol. 37, 911-917 (1959).
46. Morrison, W. R. & Smith, L. M. Preparation of fatty acid methyl esters and dimethylacetals from lipids with boron fluoride-methanol. J. Lipid Res. 5, 600-608 (1964).
47. Das, A. K. & Hajra, A. K. Quantification, characterization and fatty acid composition of lysophosphatidic acid in different rat tissues. Lipids 24, 329-333 (1989).
48. Wright, R. S. A reagent for the non-destructive location of steroids and some other lipophilic materials on silica gel thin-layer chromatograms. J. Chromatogr. 59, 220-221 (1971).