Yamauchi Ken, Phan Keith D, Butler Samantha J
Department of Biological Sciences, University of Southern California, Los Angeles, CA 90089, USA.
Development. 2008 Mar;135(6):1119-28. doi: 10.1242/dev.012989. Epub 2008 Feb 13.
The finding that morphogens, signalling molecules that specify cell identity, also act as axon guidance molecules has raised the possibility that the mechanisms that establish neural cell fate are also used to assemble neuronal circuits. It remains unresolved, however, how cells differentially transduce the cell fate specification and guidance activities of morphogens. To address this question, we have examined the mechanism by which the Bone morphogenetic proteins (BMPs) guide commissural axons in the developing spinal cord. In contrast to studies that have suggested that morphogens direct axon guidance decisions using non-canonical signal transduction factors, our results indicate that canonical components of the BMP signalling pathway, the type I BMP receptors (BMPRs), are both necessary and sufficient to specify the fate of commissural neurons and guide their axonal projections. However, whereas the induction of cell fate is a shared property of both type I BMPRs, axon guidance is chiefly mediated by only one of the type I BMPRs, BMPRIB. Taken together, these results indicate that the diverse activities of BMP morphogens can be accounted for by the differential use of distinct components of the canonical BMPR complex.
形态发生素是一类决定细胞身份的信号分子,同时也作为轴突导向分子,这一发现引发了一种可能性,即建立神经细胞命运的机制也被用于组装神经元回路。然而,细胞如何差异地转导形态发生素的细胞命运指定和导向活性仍未得到解决。为了解决这个问题,我们研究了骨形态发生蛋白(BMPs)在发育中的脊髓中引导连合轴突的机制。与那些认为形态发生素使用非经典信号转导因子来指导轴突导向决定的研究不同,我们的结果表明,BMP信号通路的经典成分,即I型BMP受体(BMPRs),对于指定连合神经元的命运和引导其轴突投射既是必要的也是充分的。然而,虽然细胞命运的诱导是两种I型BMPRs的共同特性,但轴突导向主要仅由一种I型BMPR,即BMPRIB介导。综上所述,这些结果表明,BMP形态发生素的多种活性可以通过对经典BMPR复合物不同成分的差异使用来解释。