Aging, Depot Origin, and Preadipocyte Gene Expression

被引:85
作者
Cartwright, Mark J. [3 ]
Schlauch, Karen [2 ,4 ]
Lenburg, Marc E. [4 ,5 ]
Tchkonia, Tamara [1 ,3 ]
Pirtskhalava, Tamar [1 ,3 ]
Cartwright, Andrew [3 ]
Thomou, Thomas [1 ,3 ]
Kirkland, James L. [1 ,3 ]
机构
[1] Mayo Clin, Robert & Arlene Kogod Ctr Aging, Rochester, MN 55905 USA
[2] Univ Nevada, Dept Biochem & Mol Biol, Reno, NV 89557 USA
[3] Boston Univ, Dept Med, Boston, MA 02215 USA
[4] Boston Univ, Dept Genet & Genom, Boston, MA 02215 USA
[5] Boston Univ, Dept Pathol & Lab Med, Boston, MA 02215 USA
来源
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES | 2010年 / 65卷 / 03期
基金
美国国家卫生研究院;
关键词
Aging; Preadipocyte; Fat cell progenitor; FED AD-LIBITUM; ADIPOSE-TISSUE; ANATOMIC SITE; ADIPOCYTE PRECURSORS; METABOLIC SYNDROME; PROGENITOR CELLS; BODY-FAT; IN-VITRO; RAT; DIFFERENTIATION;
D O I
10.1093/gerona/glp213
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
Fat distribution changes with aging. Inherent changes in fat cell progenitors may contribute because fat cells turn over throughout life. To define mechanisms, gene expression was profiled in preadipocytes cultured from epididymal and perirenal depots of young and old rats. 8.4% of probe sets differed significantly between depots, particularly developmental genes. Only 0.02% differed with aging, despite using less stringent criteria than for comparing depots. Twenty-five genes selected based on fold change with aging were analyzed in preadipocytes from additional young, middle-aged, and old animals by polymerase chain reaction. Thirteen changed significantly with aging, 13 among depots, and 9 with both. Genes involved in inflammation, stress, and differentiation changed with aging, as occurs in fat tissue. Age-related changes were greater in perirenal than epididymal preadipocytes, consistent with larger declines in replication and adipogenesis in perirenal preadipocytes. Thus. age-related changes in preadipocyte gene expression differ among depots, potentially contributing to fat redistribution and dysfunction.
引用
收藏
页码:242 / 251
页数:10
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