Institute of Molecular Life Sciences, University of Zurich, 8057 Zurich, Switzerland.
Nat Cell Biol. 2011 Jan;13(1):79-86. doi: 10.1038/ncb2138. Epub 2010 Dec 19.
Multicellular animals rapidly clear dying cells from their bodies. Many of the pathways that mediate this cell removal are conserved through evolution. Here, we identify srgp-1 as a negative regulator of cell clearance in both Caenorhabditis elegans and mammalian cells. Loss of srgp-1 function results in improved engulfment of apoptotic cells, whereas srgp-1 overexpression inhibits apoptotic cell corpse removal. We show that SRGP-1 functions in engulfing cells and functions as a GTPase activating protein (GAP) for CED-10 (Rac1). Interestingly, loss of srgp-1 function promotes not only the clearance of already dead cells, but also the removal of cells that have been brought to the verge of death through sublethal apoptotic, necrotic or cytotoxic insults. In contrast, impaired engulfment allows damaged cells to escape clearance, which results in increased long-term survival. We propose that C. elegans uses the engulfment machinery as part of a primitive, but evolutionarily conserved, survey mechanism that identifies and removes unfit cells within a tissue.
多细胞动物能迅速清除体内死亡的细胞。许多介导细胞清除的途径在进化过程中是保守的。在这里,我们确定 srgp-1 是秀丽隐杆线虫和哺乳动物细胞中细胞清除的负调控因子。srgp-1 功能丧失会导致凋亡细胞的吞噬作用增强,而过表达 srgp-1 会抑制凋亡细胞尸体的清除。我们表明,SRGP-1 可以在吞噬细胞中发挥作用,并作为 CED-10(Rac1)的 GTP 酶激活蛋白(GAP)。有趣的是,srgp-1 功能丧失不仅促进了已经死亡细胞的清除,还促进了通过亚致死性凋亡、坏死或细胞毒性损伤而接近死亡的细胞的清除。相比之下,吞噬作用受损会使受损细胞逃避清除,从而导致长期存活率增加。我们提出,秀丽隐杆线虫将吞噬机制作为其识别和清除组织内不适宜细胞的原始但进化上保守的检测机制的一部分。