Subcutaneous fat in normal and diseased states - 3. Adipogenesis: From stem cell to fat cell

被引:137
作者
Avram, Mathew M.
Avram, Alison Sharpe
James, William D.
机构
[1] Massachusetts Gen Hosp, Dermatol Laser & Cosmet Ctr, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Dept Dermatol, Boston, MA 02114 USA
[3] Univ Penn, Dept Dermatol, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/j.jaad.2006.06.022
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The quest for effective strategies to treat obesity has propelled fat research into an exploration of the molecular processes that drive adipocyte formation, and hence body fat mass. The development of obesity is dependent on the coordinated interplay of adipocyte hypertrophy (increased fat cell size), adipocyte hyperplasia (increased fat cell number), and angiogenesis. Evidence suggests that adipocyte hyperplasia, or adipogenesis, occurs throughout life, both in response to normal cell turnover as well as in response to the need for additional fat mass stores that arises when caloric intake exceeds nutritional requirements. Adipogenesis involves two major events-the recruitment and proliferation of adipocyte precursor cells, called preadipocytes, followed by the subsequent conversion of preadipocytes, or differentiation, into mature fat cells. in vitro studies using experimental and primary preadipocyte cell lines have uncovered the mechanisms that drive the adipogenic process, a tightly controlled sequence of events guided by the strict temporal regulation of multiple inhibitory and stimulatory signaling events involving regulators of cell-cycle functions and differentiation factors. This article reviews the current understanding of adipogenesis with emphasis on the various stages of adipocyte development; on key hormonal, nutritional, paracrine, and neuronal control signals; as well as on the components involved in cell-cell or cell-matrix interactions that are pivotal in regulating fat cell formation. Special consideration is given to clinical applications derived from adipogenesis research with impact on medical, surgical and cosmetic fields.
引用
收藏
页码:472 / 492
页数:21
相关论文
共 256 条
[51]   Functional studies of mesenchymal stem cells derived from adult human adipose tissue [J].
Dicker, A ;
Le Blanc, K ;
Åström, G ;
van Harmelen, V ;
Götherström, C ;
Blomqvist, L ;
Arner, P ;
Rydén, M .
EXPERIMENTAL CELL RESEARCH, 2005, 308 (02) :283-290
[52]  
DOGLIO A, 1986, BIOCHEM J, V238, P123, DOI 10.1042/bj2380123
[53]   Will reducing adipogenesis in bone increase bone mass?:: PPARγ2 as a key target in the treatment of age-related bone loss [J].
Duque, G .
DRUG NEWS & PERSPECTIVES, 2003, 16 (06) :341-346
[54]  
DZUBOW LM, 1998, BAS CLIN DERMATOL, V15, P1
[55]   A DIET HIGH IN FAT STIMULATES ADIPOCYTE PROLIFERATION IN OLDER (22 MONTH) RATS [J].
ELLIS, JR ;
MCDONALD, RB ;
STERN, JS .
EXPERIMENTAL GERONTOLOGY, 1990, 25 (02) :141-148
[56]   Relationship between replication and differentiation in cultured human adipocyte precursor cells [J].
Entenmann, G ;
Hauner, H .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1996, 270 (04) :C1011-C1016
[57]   The biology of somatotropin in adipose tissue growth and nutrient partitioning [J].
Etherton, TD .
JOURNAL OF NUTRITION, 2000, 130 (11) :2623-2625
[58]   Adipogenesis: a cross-talk between cell proliferation and cell differentiation [J].
Fajas, L .
ANNALS OF MEDICINE, 2003, 35 (02) :79-85
[59]   DIET-INDUCED ADIPOCYTE NUMBER INCREASE IN ADULT RATS - NEW MODEL OF OBESITY [J].
FAUST, IM ;
JOHNSON, PR ;
STERN, JS ;
HIRSCH, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1978, 235 (03) :E279-E286
[60]  
FAUST IM, 1984, EATING ITS DISORDERS, P97