Bone morphogenetic protein and retinoic acid signaling cooperate to induce osteoblast differentiation of preadipocytes

被引:187
作者
Skillington, J
Choy, L
Derynck, R [1 ]
机构
[1] Univ Calif San Francisco, Dept Growth & Dev, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Cell Biol Program, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Program Dev Biol, San Francisco, CA 94143 USA
关键词
mesenchymal; transdifferentiation; cbfa1;
D O I
10.1083/jcb.200204060
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mesenchymal cells can differentiate into osteoblasts, adipocytes, myoblasts, or chondroblasts. Whether mesenchymal cells that have initiated differentiation along one lineage can transdifferentiate into another is largely unknown. Using 3T3-F442A preadipocytes, we explored whether extracellular signals could redirect their differentiation from adipocyte into osteoblast. 3T3-F442A cells expressed receptors and Smads required for bone morphogenetic protein (BMP) signaling. BMP-2 increased proliferation and induced the early osteoblast differentiation marker alkaline phosphatase, yet only mildly affected adipogenic differentiation. Retinoic acid inhibited adipose conversion and cooperated with BMP-2 to enhance proliferation, inhibit adipogenesis, and promote early osteoblastic differentiation. Expression of BMP-RII together with BMP-RIA or BMP-RIB suppressed adipogenesis of 3T3-F442A cells and promoted full osteoblastic differentiation in response to retinoic acid. Osteoblastic differentiation was characterized by induction of cbfa1, osteocalcin, and collagen I expression, and extracellular matrix calcification. These results indicate that 3T3-F442A preadipocytes can be converted into fully differentiated osteoblasts in response to extracellular signaling cues. Furthermore, BMP and retinoic acid signaling cooperate to stimulate cell proliferation, repress adipogenesis, and promote osteoblast differentiation. Finally, BMP-RIA and BMP-RIB induced osteoblast differentiation and repressed adipocytic differentiation to a similar extent.
引用
收藏
页码:135 / 146
页数:12
相关论文
共 84 条
[51]   Influence of mature adipocytes on osteoblast proliferation in human primary cocultures [J].
Maurin, AC ;
Chavassieux, PM ;
Frappart, L ;
Delmas, PD ;
Serre, CM ;
Meunier, PJ .
BONE, 2000, 26 (05) :485-489
[52]   Regulation of skeletal muscle mass in mice by a new TGF-beta superfamily member [J].
McPherron, AC ;
Lawler, AM ;
Lee, SJ .
NATURE, 1997, 387 (6628) :83-90
[53]  
Meunier P, 1971, CLIN ORTHOP RELAT R, V80, P147, DOI DOI 10.1097/00003086-197110000-00021
[54]  
MILLER AD, 1989, BIOTECHNIQUES, V7, P980
[55]  
Muraglia A, 2000, J CELL SCI, V113, P1161
[56]  
Nakayama T, 1998, DEVELOPMENT, V125, P857
[57]   A kinase domain-truncated type I receptor blocks bone morphogenetic protein-2-induced signal transduction in C2C12 myoblasts [J].
Namiki, M ;
Akiyama, S ;
Katagiri, T ;
Suzuki, A ;
Ueno, N ;
Yamaji, N ;
Rosen, V ;
Wozney, JM ;
Suda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (35) :22046-22052
[58]   Smad5 and DPC4 are key molecules in mediating BMP-2-induced osteoblastic differentiation of the pluripotent mesenchymal precursor cell fine C2C12 [J].
Nishimura, R ;
Kato, Y ;
Chen, D ;
Harris, SE ;
Mundy, GR ;
Yoneda, T .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (04) :1872-1879
[59]   IDENTIFICATION OF A HUMAN TYPE-II RECEPTOR FOR BONE MORPHOGENETIC PROTEIN-4 THAT FORMS DIFFERENTIAL HETEROMERIC COMPLEXES WITH BONE MORPHOGENETIC PROTEIN TYPE-I RECEPTORS [J].
NOHNO, T ;
ISHIKAWA, T ;
SAITO, T ;
HOSOKAWA, K ;
NOJI, S ;
WOLSING, DH ;
ROSENBAUM, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (38) :22522-22526
[60]  
OLSON EN, 1986, J CELL BIOL, V103, P1799, DOI 10.1083/jcb.103.5.1799