Stott N S, Jiang T X, Chuong C M
Department of Pathology, University of Southern California, Los Angeles 90033, USA.
J Cell Physiol. 1999 Sep;180(3):314-24. doi: 10.1002/(SICI)1097-4652(199909)180:3<314::AID-JCP2>3.0.CO;2-Y.
High-density chick limb bud cell culture is a useful model to study mesenchymal condensatifons and chondrogenesis. Most previous studies have focused on the effects of soluble reagents on terminal chondrogenic differentiation and have not defined the early cellular processes and signaling events. In this study, we defined five successive stages in the differentiation process: 1) dissociated cells, 2) small aggregates, 3) formation of cell clusters, 4) precartilaginous condensations, and 5) cartilage nodule. We used RCAS retrovirus-mediated Wnt-7a gene transduction to test the effect of Wnt-7a on the differentiation process. We found that Wnt-7a suppressed chondrogenic differentiation. Wnt-7a did not inhibit the initiation of condensation formation but blocked the progression of precartilaginous condensations to cartilage nodules. The Wnt-7a-transduced cultures showed characteristics of a less mature culture with persistent expression of NCAM, N-cadherin, wider distribution of integrin beta1 and fibronectin, and suppression of tenascin-C. BMP-2 is known to enhance chondrogenic differentiation in these cultures by promoting cell clusters to form continuous sheet-like precartilaginous condensations. However, cultures exposed to both BMP-2 and Wnt-7a showed inhibition of chondrogenic differentiation. Different signaling molecules such as Wnt-7a and BMP-2 may have antagonistic effects on cartilage differentiation and the gradient of the two molecules may be involved in defining the boundaries of the initial precartilaginous condensation. We propose that the shape of the precartilaginous condensations may be modulated by local concentrations of signaling molecules, such as Wnt-7a and BMP-2, which act to alter cell-substrate and cell-cell adhesions.
高密度鸡胚肢芽细胞培养是研究间充质凝聚和软骨形成的有用模型。以往大多数研究都集中在可溶性试剂对终末软骨分化的影响上,尚未明确早期细胞过程和信号事件。在本研究中,我们定义了分化过程中的五个连续阶段:1)解离细胞,2)小聚集体,3)细胞簇形成,4)软骨前凝聚,5)软骨结节。我们使用RCAS逆转录病毒介导的Wnt-7a基因转导来测试Wnt-7a对分化过程的影响。我们发现Wnt-7a抑制软骨分化。Wnt-7a不抑制凝聚形成的起始,但阻止软骨前凝聚向软骨结节的进展。转导Wnt-7a的培养物表现出较不成熟培养物的特征,持续表达NCAM、N-钙黏蛋白,整合素β1和纤连蛋白分布更广泛,腱生蛋白-C受到抑制。已知BMP-2通过促进细胞簇形成连续的片状软骨前凝聚来增强这些培养物中的软骨分化。然而,同时暴露于BMP-2和Wnt-7a的培养物显示软骨分化受到抑制。不同的信号分子如Wnt-7a和BMP-2可能对软骨分化具有拮抗作用,这两种分子的梯度可能参与确定初始软骨前凝聚的边界。我们提出,软骨前凝聚的形状可能受到信号分子如Wnt-7a和BMP-2局部浓度的调节,这些信号分子作用于改变细胞-基质和细胞-细胞黏附。