Inhibition of chondrogenesis by wnt gene expression in vivo and in vitro

被引:159
作者
Rudnicki, JA
Brown, AMC
机构
[1] CORNELL UNIV,GRAD SCH MED SCI,CELL BIOL & GENET PROGRAM,NEW YORK,NY 10021
[2] CORNELL UNIV,COLL MED,DEPT CELL BIOL & ANAT,NEW YORK,NY 10021
关键词
PROTO-ONCOGENE INT-1; CHICK LIMB BUD; PRECARTILAGINOUS MESENCHYMAL CONDENSATIONS; GAP JUNCTIONAL COMMUNICATION; MAMMARY EPITHELIAL-CELLS; APICAL ECTODERMAL RIDGE; N-CADHERIN EXPRESSION; XENOPUS EMBRYOS; CARTILAGE DIFFERENTIATION; GROWTH-FACTOR;
D O I
10.1006/dbio.1997.8536
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Wnt family of secreted signaling proteins are implicated in regulating morphogenesis and tissue patterning in a wide variety of organ systems. Several Wnt genes are expressed in the developing limbs and head, implying roles in skeletal development. To explore these functions, we have used retroviral gene transfer to express Wnt-1 ectopically in the limb buds and craniofacial region of chick embryos. Infection of wing buds at stage 17 and tissues in the head at stage 10 resulted in skeletal abnormalities whose most consistent defects suggested a localized failure of cartilage formation. To test this hypothesis, we infected micromass cultures of prechondrogenic mesenchyme in vitro and found that expression of Wnt-1 caused a severe block in chondrogenesis. Wnt-7a, a gene endogenously expressed in the limb and facial ectoderm, had a similar inhibitory effect. Further analysis of this phenomenon in vitro showed that Wnt-1 and Wnt-7a had mitogenic effects only in early prechondrogenic mesenchyme, that cell aggregation and formation of the prechondrogenic blastema occurred normally, and that the block to differentiation was at the late-blastema/early-chondroblast stage. These results indicate that Wnt signals can have specific inhibitory effects on cytodifferentiation and suggest that one function of endogenous Wnt proteins in the limbs and face may be to influence skeletal morphology by localized inhibition of chondrogenesis. (C) 1997 Academic Press.
引用
收藏
页码:104 / 118
页数:15
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