The Changing Balance Between Osteoblastogenesis and Adipogenesis in Aging and its Impact on Hematopoiesis

被引:98
作者
Bethel, Monique [1 ]
Chitteti, Brahmananda R. [2 ]
Srour, Edward F. [3 ,4 ,5 ]
Kacena, Melissa A. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Orthopaed Surg, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Med, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Med, Indianapolis, IN 46202 USA
[4] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Pediat, Indianapolis, IN 46202 USA
[5] Indiana Univ Sch Med, Herman B Wells Ctr Pediat Res, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
关键词
Mesenchymal stem cells; Adipocyte; Osteoblast; Aging; Osteoporosis; Hematopoiesis; HUMAN BONE-MARROW; MESENCHYMAL STEM-CELLS; BETA-CATENIN; OSTEOGENIC DIFFERENTIATION; PROGENITOR CELLS; GENE-EXPRESSION; GROWTH-FACTOR; LIFE-SPAN; WNT; ADIPOCYTES;
D O I
10.1007/s11914-013-0135-6
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Osteoblasts (OBs) and adipocytes (APs) share a common mesenchymal ancestor. It is now clear that mesenchymal stem cell (MSC) maturation along the OB lineage comes at the expense of adipogenesis and vice versa. During aging, this balance increasingly favors the formation of APs. Hematopoiesis also slowly declines during the aging process. The role of OB lineage cells in hematopoiesis has been studied, but less is known about how APs regulate hematopoiesis. A few studies have demonstrated a negative relationship between APs and hematopoiesis; however, there is also evidence that brown adipose tissue (BAT) may promote hematopoiesis. This review will examine the current knowledge of how adipogenesis and osteogenesis change with aging and the implications of this changing environment on hematopoeisis.
引用
收藏
页码:99 / 106
页数:8
相关论文
共 72 条
[61]
Telomerase expression extends the proliferative life-span and maintains the osteogenic potential of human bone marrow stromal cells [J].
Simonsen, JL ;
Rosada, C ;
Serakinci, N ;
Justesen, J ;
Stenderup, K ;
Rattan, SIS ;
Jensen, TG ;
Kassem, M .
NATURE BIOTECHNOLOGY, 2002, 20 (06) :592-596
[62]
Sohal R.S., 1985, BASIC LIFE SCI, V35, P75, DOI DOI 10.1007/978-1-4899-2218-2_4
[63]
SPANGRUDE GJ, 1988, J IMMUNOL, V141, P3697
[64]
Aging is associated with decreased maximal life span and accelerated senescence of bone marrow stromal cells [J].
Stenderup, K ;
Justesen, J ;
Clausen, C ;
Kassem, M .
BONE, 2003, 33 (06) :919-926
[65]
MODIFICATION OF STRAIN-SPECIFIC FEMORAL BONE-DENSITY BY BONE-MARROW-DERIVED FACTORS ADMINISTERED NEONATALLY - A STUDY ON THE SPONTANEOUSLY OSTEOPOROTIC MOUSE, SAMP6 [J].
TAKAHASHI, K ;
TSUBOYAMA, T ;
MATSUSHITA, M ;
KASAI, R ;
OKUMURA, H ;
YAMAMURO, T ;
OKAMOTO, Y ;
TORIYAMA, K ;
KITAGAWA, K ;
TAKEDA, T .
BONE AND MINERAL, 1994, 24 (03) :245-255
[66]
HO-1 expression increases mesenchymal stem cell-derived osteoblasts but decreases adipocyte lineage [J].
Vanella, Luca ;
Kim, Dong Hyun ;
Asprinio, David ;
Peterson, Stephen J. ;
Barbagallo, Ignazio ;
Vanella, Angelo ;
Goldstein, Dove ;
Ikehara, Susumu ;
Kappas, Attallah ;
Abraham, Nader G. .
BONE, 2010, 46 (01) :236-243
[67]
Impairment of osteoblast differentiation due to proliferation-independent telomere dysfunction in mouse models of accelerated aging [J].
Wang, Haitao ;
Chen, Qijun ;
Lee, Seoung-Hoon ;
Choi, Yongwon ;
Johnson, Frederick Brad ;
Pignolo, Robert J. .
AGING CELL, 2012, 11 (04) :704-713
[68]
Stem cells and aging in the hematopoietic system [J].
Warren, Luigi A. ;
Rossi, Derrick J. .
MECHANISMS OF AGEING AND DEVELOPMENT, 2009, 130 (1-2) :46-53
[69]
Oscillations in total body fat content through life: an evolutionary perspective [J].
Zafon, C. .
OBESITY REVIEWS, 2007, 8 (06) :525-530
[70]
Age-related intrinsic changes in human bone-marrow-derived mesenchymal stem cells and their differentiation to osteoblasts [J].
Zhou, Shuanhu ;
Greenberger, Joel S. ;
Epperly, Michael W. ;
Goff, Julie P. ;
Adler, Carolyn ;
LeBoff, Meryl S. ;
Glowacki, Julie .
AGING CELL, 2008, 7 (03) :335-343