Bergmann Andreas, Tugentman Michael, Shilo Ben Zion, Steller Hermann
Department of Biology, Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Dev Cell. 2002 Feb;2(2):159-70. doi: 10.1016/s1534-5807(02)00116-8.
Trophic mechanisms in which neighboring cells mutually control their survival by secreting extracellular factors play an important role in determining cell number. However, how trophic signaling suppresses cell death is still poorly understood. We now show that the survival of a subset of midline glia cells in Drosophila depends upon direct suppression of the proapoptotic protein HID via the EGF receptor/RAS/MAPK pathway. The TGFalpha-like ligand SPITZ is activated in the neurons, and glial cells compete for limited amounts of secreted SPITZ to survive. In midline glia that fail to activate the EGFR pathway, HID induces apoptosis by blocking a caspase inhibitor, Diap1. Therefore, a direct pathway linking a specific extracellular survival factor with a caspase-based death program has been established.
相邻细胞通过分泌细胞外因子相互控制生存的营养机制在决定细胞数量方面发挥着重要作用。然而,营养信号如何抑制细胞死亡仍知之甚少。我们现在表明,果蝇中线神经胶质细胞亚群的存活取决于通过表皮生长因子受体/ RAS/丝裂原活化蛋白激酶途径直接抑制促凋亡蛋白HID。类转化生长因子α配体SPITZ在神经元中被激活,神经胶质细胞通过竞争有限量分泌的SPITZ来存活。在未能激活表皮生长因子受体途径的中线神经胶质细胞中,HID通过阻断半胱天冬酶抑制剂Diap1诱导细胞凋亡。因此,已经建立了一条将特定细胞外存活因子与基于半胱天冬酶的死亡程序联系起来的直接途径。