González-Estévez Cristina, Felix Daniel A, Aboobaker Aziz A, Saló Emili
Departament de Genètica, Facultat de Biologia, Universitat de Barcelona, Barcelona, Spain.
Autophagy. 2007 Nov-Dec;3(6):640-2. doi: 10.4161/auto.4934. Epub 2007 Aug 24.
Planarians have been established as an ideal model organism for stem cell research and regeneration. Planarian regeneration and homeostasis require an exquisite balancing act between cell death and cell proliferation as new tissues are made (epimorphosis) and existing tissues remodeled (morphallaxis). Some of the genes and mechanisms that control cell proliferation and pattern formation are known. However, studies about cell death during remodeling are few and far between. We have studied the gene Gtdap-1, the planarian ortholog of human death-associated protein-1 or DAP-1. DAP-1 together with DAP-kinase has been identified as a positive mediator of programmed cell death induced by gamma-interferon in HeLa cells. We have found that the gene functions at the interface between autophagy and cell death in the remodeling of the organism that occurs during regeneration and starvation in sexual and asexual races of planarians. Our data suggest that autophagy of existing cells may be essential to fuel the continued proliferation and differentiation of stem cells by providing the necessary energy and building blocks to neoblasts.
涡虫已成为干细胞研究和再生的理想模式生物。涡虫的再生和体内平衡需要在细胞死亡和细胞增殖之间进行精确的平衡,因为新组织形成(形态发生)且现有组织重塑(组织再生)。一些控制细胞增殖和模式形成的基因和机制已为人所知。然而,关于重塑过程中细胞死亡的研究却寥寥无几。我们研究了基因Gtdap - 1,它是人类死亡相关蛋白 - 1(DAP - 1)的涡虫直系同源基因。DAP - 1与DAP激酶一起被确定为γ - 干扰素在HeLa细胞中诱导程序性细胞死亡的正向介质。我们发现该基因在涡虫有性和无性生殖系再生和饥饿期间发生的生物体重塑过程中的自噬与细胞死亡之间的界面发挥作用。我们的数据表明,现有细胞的自噬对于通过为新生细胞提供必要的能量和构建块来推动干细胞的持续增殖和分化可能至关重要。