Aging in adipocytes: Potential impact of inherent, depot-specific mechanisms

被引:252
作者
Cartwright, Mark J. [1 ]
Tchkonia, Tamara [1 ]
Kirkland, James L. [1 ]
机构
[1] Boston Univ, Med Ctr, Dept Med, Sect Geriatr, Boston, MA 02118 USA
关键词
C/EBP alpha; PPAR gamma; CUGBP; preadipocyte differentiation; dysdifferentiation;
D O I
10.1016/j.exger.2007.03.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 [法学]; 0303 [社会学]; 100203 [老年医学];
摘要
Fat mass and tissue distribution change dramatically throughout life. Fat depot sizes reach a peak by middle or early old age, followed by a substantial decline, together with fat tissue dysfunction and redistribution in advanced old age. These changes ate associated with health complications, including type 2 diabetes, atherosclerosis, dyslipidemia, thermal dysregulation, and skin ulcers, particularly in advanced old age. Fat tissue growth occurs through increases in size and number of fat cells. Fat cells turn over throughout the lifespan, with new fat cells developing from preadipocytes, which are of mesenchymal origin. The pool of preadipocytes comprises 15-50% of the cells in fat tissue. Since fat tissue turns over throughout life, characteristics of these cells very likely have a significant impact on fat tissue growth, plasticity, function, and distribution. The aims of this review are to highlight recent findings regarding changes in preadipocyte cell dynamics and function with aging, and to consider how inherent characteristics of these cells potentially contribute to age- and depot-dependent changes in fat tissue development and function. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:463 / 471
页数:9
相关论文
共 77 条
[1]
Epidermal growth factor receptor stimulation activates the RNA bindin protein CUG-BP1 and increases expression of C/EBPβ-LIP in mammary epithelial cells [J].
Baldwin, BR ;
Timchenko, NA ;
Zahnow, CA .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (09) :3682-3691
[2]
INHIBITION OF ADIPOGENESIS BY THE STRESS-INDUCED PROTEIN CHOP (GADD153) [J].
BATCHVAROVA, N ;
WANG, XZ ;
RON, D .
EMBO JOURNAL, 1995, 14 (19) :4654-4661
[3]
Oxidative and nonoxidative glucose disposal in elderly vs younger men with similar and smaller body mass indices and waist circumferences [J].
Bryhni, B ;
Jenssen, TG ;
Olafsen, K ;
Bendikssen, A .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2005, 54 (06) :748-755
[4]
CCAAT/enhancer binding protein α (CIEBPα) is an important mediator of mouse C/EBPβ protein isoform production [J].
Burgess-Beusse, BL ;
Timchenko, NA ;
Darlington, GJ .
HEPATOLOGY, 1999, 29 (02) :597-601
[5]
Diseases of adipose tissue:: genetic and acquired lipodystrophies [J].
Capeau, J ;
Magré, J ;
Lascols, O ;
Caron, M ;
Béréziat, V ;
Vigouroux, C ;
Bastard, JP .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2005, 33 :1073-1077
[6]
Preadipocyte conversion to macrophage -: Evidence of plasticity [J].
Charrière, G ;
Cousin, B ;
Arnaud, E ;
André, M ;
Bacou, F ;
Pénicaud, L ;
Casteilla, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (11) :9850-9855
[7]
Nuclear receptors and lipid physiology: Opening the X-files [J].
Chawla, A ;
Repa, JJ ;
Evans, RM ;
Mangelsdorf, DJ .
SCIENCE, 2001, 294 (5548) :1866-1870
[8]
CHUMLEA W C, 1989, American Journal of Human Biology, V1, P457, DOI 10.1002/ajhb.1310010408
[9]
Preadipocytes mediate lipopolysaccharide-induced inflammation and insulin resistance in primary cultures of newly differentiated human adipocytes [J].
Chung, Soonkyu ;
LaPoint, Kathleen ;
Martinez, Kristina ;
Kennedy, Arion ;
Sandberg, Maria Boysen ;
McIntosh, Michael K. .
ENDOCRINOLOGY, 2006, 147 (11) :5340-5351
[10]
CAAT/enhancer binding proteins directly modulate transcription from the peroxisome proliferator-activated receptor gamma 2 promoter [J].
Clarke, SL ;
Robinson, CE ;
Gimble, JM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (01) :99-103