Ziman Benjamin, Barghouth Paul G, Maciel Eli Isael, Oviedo Néstor J
Department of Molecular and Cell Biology, University of California, Merced, CA 95343, USA.
Quantitative and Systems Biology Graduate Program, University of California, Merced, CA 95343, USA.
iScience. 2020 Oct 9;23(11):101665. doi: 10.1016/j.isci.2020.101665. eCollection 2020 Nov 20.
Tissue homeostasis relies on the timely renewal of cells that have been damaged or have surpassed their biological age. Nonetheless, the underlying molecular mechanism coordinating tissue renewal is unknown. The planarian harbors a large population of stem cells that continuously divide to support the restoration of tissues throughout the body. Here, we identify that TNF Receptor Associated Factors (TRAFs) play critical roles in cellular survival during tissue repair in . . Disruption with RNA-interference of TRAF signaling results in rapid morphological defects and lethality within 2 weeks. The TRAF phenotype is accompanied by an increased number of mitoses and cell death. Our results also reveal TRAF signaling is required for proper regeneration of the nervous system. Taken together, we find functional conservation of TRAF-like proteins in . as they act as crucial regulators of cellular survival during tissue homeostasis and regeneration.
组织稳态依赖于对受损或已超过其生物学年龄的细胞进行及时更新。然而,协调组织更新的潜在分子机制尚不清楚。涡虫含有大量干细胞,这些干细胞持续分裂以支持全身组织的修复。在此,我们发现肿瘤坏死因子受体相关因子(TRAFs)在涡虫组织修复过程中的细胞存活中起关键作用。用RNA干扰TRAF信号会导致在2周内迅速出现形态缺陷和致死性。TRAF表型伴随着有丝分裂数量增加和细胞死亡。我们的结果还表明,TRAF信号对于神经系统的正常再生是必需的。综上所述,我们发现涡虫中TRAF样蛋白具有功能保守性,因为它们在组织稳态和再生过程中作为细胞存活的关键调节因子发挥作用。