Differential expression of cytokines in subcutaneous and marrow fat of aging C57BL/6J mice

被引:54
作者
Gasparrini, Marco [2 ]
Rivas, Daniel [2 ]
Elbaz, Alexandre [2 ]
Duque, Gustavo [1 ,2 ]
机构
[1] Univ Sydney, Aging Bone Res Program, Nepean Clin Sch, Penrith, NSW 2750, Australia
[2] McGill Univ, Lady Davis Inst Med Res, Montreal, PQ, Canada
基金
加拿大健康研究院;
关键词
Bone marrow fat; Apoptosis; Osteoporosis; Adipokines; Cytokines; Subcutaneous fat; Osteoblast; Adipocytes; Osteoclast; Lipotoxicity; INDUCED OSTEOCLAST FORMATION; BONE-MARROW; INTERFERON-GAMMA; ADIPOSE-TISSUE; STEM-CELLS; ADIPOGENESIS; METABOLISM; APOPTOSIS; PROLIFERATION; OSTEOPOROSIS;
D O I
10.1016/j.exger.2009.05.009
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
030301 [社会学]; 100201 [内科学];
摘要
Increasing marrow adipogenesis plays a causative role in the pathogenesis of age-related bone loss that could be associated with high cytokine production. In this study, we characterized the age-related changes in cytokine expression by bone marrow (BM) adipocytes as compared with subcutaneous (SC) fat. BM and SC adipocytes were isolated from young (4 months) and old (24 months) male C57BL/6J. Total proteins were extracted and proteomic analysis of 96 cytokines was performed using a cytokine antibody array. Proteins showing a significant change were grouped according with their known function in bone. We found a significant age-induced difference in the expression of 53 cytokines. As compared with SC adipocytes, aging BM adipocytes showed a more pro-adipogenic, anti-osteoblastogenic and pro-apoptotic phenotype. These data suggest that, with aging, BM adipocytes become significantly more toxic than SC adipocytes. These cytokines, if secreted, could play a role in the pathogenesis of age-related bone loss by affecting other cells within the marrow milieu. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:613 / 618
页数:6
相关论文
共 46 条
[1]
Effects of basic fibroblast growth factor and a prostaglandin E2 receptor subtype 4 agonist on osteoblastogenesis and adipogenesis in aged ovariectomized rats [J].
Aguirre, J. Ignacio ;
Leal, Martha E. ;
Rivera, Mercedes F. ;
Vanegas, Sally M. ;
Jorgensen, Marda ;
Wronski, Thomas J. .
JOURNAL OF BONE AND MINERAL RESEARCH, 2007, 22 (06) :877-888
[2]
Adipose tissue as an endocrine organ [J].
Ahima, Rexford S. .
OBESITY, 2006, 14 :242-249
[3]
Expression and regulation of osteoprotegefin in adipose tissue [J].
An, Juan-Ji ;
Han, Dong-He ;
Kim, Dol-Mi ;
Kim, Se-Hwa ;
Rhee, Yurnie ;
Lee, Eun-Jig ;
Lim, Sung-Kil .
YONSEI MEDICAL JOURNAL, 2007, 48 (05) :765-772
[4]
Proteomics reveals multiple routes to the osteogenic phenotype in mesenchymal stem cells [J].
Bennett, Kristin P. ;
Bergeron, Charles ;
Acar, Evrim ;
Klees, Robert F. ;
Vandenberg, Scott L. ;
Yener, Bulent ;
Plopper, George E. .
BMC GENOMICS, 2007, 8 (1)
[5]
Bunnell Bruce A., 2008, V456, P155, DOI 10.1007/978-1-59745-245-8_12
[6]
Gelatinase B(MMP-9) an apoptotic factor in diabetic transgenic mice [J].
Camp, TM ;
Tyagi, SC ;
Senior, RM ;
Hayden, MR ;
Tyagi, SC .
DIABETOLOGIA, 2003, 46 (10) :1438-1445
[7]
Aging increases stromal/osteoblastic cell-induced osteoclastogenesis and alters the osteoclast precursor pool in the mouse [J].
Cao, JJ ;
Wronski, TJ ;
Iwaniec, U ;
Phleger, L ;
Kurimoto, P ;
Boudignon, B ;
Halloran, BP .
JOURNAL OF BONE AND MINERAL RESEARCH, 2005, 20 (09) :1659-1668
[8]
Aging in adipocytes: Potential impact of inherent, depot-specific mechanisms [J].
Cartwright, Mark J. ;
Tchkonia, Tamara ;
Kirkland, James L. .
EXPERIMENTAL GERONTOLOGY, 2007, 42 (06) :463-471
[9]
Age-related bone loss: Old bone, new facts [J].
Chan, GK ;
Duque, G .
GERONTOLOGY, 2002, 48 (02) :62-71
[10]
Modulation of Osteoclastogenesis by Fatty Acids [J].
Cornish, Jillian ;
MacGibbon, Alastair ;
Lin, Jian-Ming ;
Watson, Maureen ;
Callon, Karen E. ;
Tong, P. C. ;
Dunford, James E. ;
van der Does, Yvonne ;
Williams, Garry A. ;
Grey, Andrew B. ;
Naot, Dorit ;
Reid, Ian R. .
ENDOCRINOLOGY, 2008, 149 (11) :5688-5695