Department of Biological Chemistry, The Weizmann Institute of Science, 76100 Rehovot, Israel.
Trends Immunol. 2011 Nov;32(11):505-9. doi: 10.1016/j.it.2011.07.004. Epub 2011 Sep 2.
Necrosis, a form of death characterized by rupture of the cell membrane, is closely interlinked with inflammation. Cellular components released during necrotic death can trigger inflammation. Conversely, inflammation often yields tissue damage and, as a consequence, cell death. Which occurs first--necrosis or inflammation--in specific in vivo situations is currently difficult to tell. A way out of this 'chicken-and-egg' conundrum may be found via the recent finding that both necrotic cell death and inflammation can be initiated by a distinct set of signaling proteins, the 'necrosome', that includes receptor-interacting protein (RIP)1, RIP3 and caspase-8. Further clarifying the function of these signaling proteins should make it possible to establish when they induce inflammation directly and when inflammation is caused by necrotic cell death.
细胞坏死是一种以细胞膜破裂为特征的死亡形式,它与炎症密切相关。坏死过程中释放的细胞成分可引发炎症。相反,炎症通常会导致组织损伤,进而导致细胞死亡。在特定的体内情况下,是先发生坏死还是炎症目前难以判断。最近的一项发现为解决这一“先有鸡还是先有蛋”的难题提供了思路,即坏死细胞死亡和炎症都可以由一组特定的信号蛋白——“坏死体”来启动,该蛋白包括受体相互作用蛋白(RIP)1、RIP3 和半胱天冬酶-8。进一步阐明这些信号蛋白的功能,将有助于确定它们何时直接引发炎症,以及何时炎症是由坏死细胞死亡引起的。