Adipose tissue stem cells meet preadipocyte commitment: going back to the future

被引:323
作者
Cawthorn, William P. [1 ]
Scheller, Erica L. [1 ]
MacDougald, Ormond A. [1 ]
机构
[1] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
adipocytes; bone marrow; signal transduction; preadipocytes; HUMAN BONE-MARROW; ADIPOCYTE PRECURSOR CLONES; IN-VITRO DIFFERENTIATION; TUMOR-NECROSIS-FACTOR; STROMAL CELLS; PROGENITOR CELLS; PPAR-GAMMA; TRANSCRIPTIONAL CONTROL; GENE-EXPRESSION; ANATOMIC SITE;
D O I
10.1194/jlr.R021089
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
White adipose tissue (WAT) is perhaps the most plastic organ in the body, capable of regeneration following surgical removal and massive expansion or contraction in response to altered energy balance. Research conducted for over 70 years has investigated adipose tissue plasticity on a cellular level, spurred on by the increasing burden that obesity and associated diseases are placing on public health globally. This work has identified committed preadipocytes in the stromal vascular fraction of adipose tissue and led to our current understanding that adipogenesis is important not only for WAT expansion, but also for maintenance of adipocyte numbers under normal metabolic states. At the turn of the millenium, studies investigating preadipocyte differentiation collided with developments in stem cell research, leading to the discovery of multipotent stem cells within WAT. Such adipose tissue-derived stem cells (ASCs) are capable of differentiating into numerous cell types of both mesodermal and nonmesodermal origin, leading to their extensive investigation from a therapeutic and tissue engineering perspective. However, the insights gained through studying ASCs have also contributed to more-recent progress in attempts to better characterize committed preadipocytes in adipose tissue. Thus, ASC research has gone back to its roots, thereby expanding our knowledge of preadipocyte commitment and adipose tissue biology.-Cawthorn, W.P., E.L. Scheller, and O.A. MacDougald. Adipose tissue stem cells meet preadipocyte commitment: going back to the future. J. Lipid Res. 2012. 53: 227-246.
引用
收藏
页码:227 / 246
页数:20
相关论文
共 255 条
[31]   Roles of autocrine TGF-β receptor and Smad signaling in adipocyte differentiation [J].
Choy, L ;
Skillington, J ;
Derynck, R .
JOURNAL OF CELL BIOLOGY, 2000, 149 (03) :667-681
[32]   Adipogenesis and WNT signalling [J].
Christodoulides, Constantinos ;
Lagathu, Claire ;
Sethi, Jaswinder K. ;
Vidal-Puig, Antonio .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2009, 20 (01) :16-24
[33]  
CINTI S, 1984, J SUBMICR CYTOL PATH, V16, P243
[34]   Microscopic studies of the new formation of fat in living adult rabbits [J].
Clark, ER ;
Clark, EL .
AMERICAN JOURNAL OF ANATOMY, 1940, 67 (02) :255-285
[35]  
Coats J, 1883, MANUAL PATHOLOGY, P123
[36]  
Conget PA, 1999, J CELL PHYSIOL, V181, P67, DOI 10.1002/(SICI)1097-4652(199910)181:1<67::AID-JCP7>3.0.CO
[37]  
2-C
[38]   Human subcutaneous adipose cells support complete differentiation but not self-renewal of hematopoietic progenitors [J].
Corre, Jill ;
Barreau, Corinne ;
Cousin, Beatrice ;
Chavoin, Jean-Pierre ;
Caton, David ;
Fournial, Gerard ;
Penicaud, Luc ;
Casteilla, Louis ;
Laharrague, Patrick .
JOURNAL OF CELLULAR PHYSIOLOGY, 2006, 208 (02) :282-288
[39]   Reconstitution of lethally irradiated mice by cells isolated from adipose tissue [J].
Cousin, B ;
André, M ;
Arnaud, E ;
Pénicaud, L ;
Casteilla, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 301 (04) :1016-1022
[40]   Adipose-derived adult stromal cells heal critical-size mouse calvarial defects [J].
Cowan, CM ;
Shi, YY ;
Aalami, OO ;
Chou, YF ;
Mari, C ;
Thomas, R ;
Quarto, N ;
Contag, CH ;
Wu, B ;
Longaker, MT .
NATURE BIOTECHNOLOGY, 2004, 22 (05) :560-567