Shklover Jeny, Levy-Adam Flonia, Kurant Estee
Department of Genetics and Developmental Biology, The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
Department of Genetics and Developmental Biology, The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion - Israel Institute of Technology, Haifa 31096, Israel.
FEBS Lett. 2015 Apr 2;589(8):871-9. doi: 10.1016/j.febslet.2015.02.032. Epub 2015 Mar 6.
Eiger, the sole Drosophila TNF-alpha homolog, causes ectopic apoptosis through JNK pathway activation. Yet, its role in developmental apoptosis remains unclear. eiger mutant flies are viable and fertile but display compromised elimination of oncogenic cells and extracellular bacteria. Here we show that Eiger, specifically expressed in embryonic neurons and glia, is not involved in developmental neuronal apoptosis or in apoptotic cell clearance. Instead, we provide evidence that Eiger is required for damage-induced apoptosis in the embryonic CNS through regulation of the pro-apoptotic gene hid independently of the JNK pathway. Our study thus reveals a new requirement for Eiger in eliminating damaged cells during development.
艾格(Eiger)是果蝇中唯一的肿瘤坏死因子-α(TNF-α)同源物,它通过激活JNK信号通路引发异位凋亡。然而,其在发育性凋亡中的作用仍不清楚。艾格突变果蝇能够存活且可育,但在清除致癌细胞和细胞外细菌方面存在缺陷。我们在此表明,特异性表达于胚胎神经元和神经胶质细胞中的艾格,并不参与发育性神经元凋亡或凋亡细胞清除过程。相反,我们有证据表明,艾格通过独立于JNK信号通路调控促凋亡基因hid,从而在胚胎中枢神经系统中对损伤诱导的凋亡是必需的。因此,我们的研究揭示了艾格在发育过程中清除受损细胞方面的新需求。