Evans E K, Lu W, Strum S L, Mayer B J, Kornbluth S
Department of Molecular Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.
EMBO J. 1997 Jan 15;16(2):230-41. doi: 10.1093/emboj/16.2.230.
Apoptosis is essential for the development and homeostasis of multicellular organisms. Recently, a cell-free extract prepared from Xenopus eggs was shown to recapitulate intracellular apoptotic pathways in vitro. While many stimuli have been shown to trigger apoptosis in a variety of cell types, the intracellular signaling pathways involved in apoptosis remain largely unknown. Here we show that addition of a recombinant protein containing the phosphotyrosine binding (SH2) domain from the adaptor protein crk, but not those derived from a panel of other signaling proteins, can prevent apoptosis in the Xenopus egg extract system. Furthermore, immunodepletion of endogenous crk protein from the egg extracts, or addition of anti-crk antisera to these extracts, prevents apoptosis. The ability to undergo apoptosis can be restored to these extracts by addition of recombinant crk protein. These results directly demonstrate that crk participates in apoptotic signaling.
细胞凋亡对于多细胞生物体的发育和体内平衡至关重要。最近,从非洲爪蟾卵制备的无细胞提取物被证明能在体外重现细胞内凋亡途径。虽然许多刺激已被证明能在多种细胞类型中触发细胞凋亡,但参与凋亡的细胞内信号通路仍大多未知。在此我们表明,添加一种含有衔接蛋白crk的磷酸酪氨酸结合(SH2)结构域的重组蛋白,而非来自一组其他信号蛋白的重组蛋白,可在非洲爪蟾卵提取物系统中阻止细胞凋亡。此外,从卵提取物中免疫去除内源性crk蛋白,或向这些提取物中添加抗crk抗血清,均可阻止细胞凋亡。通过添加重组crk蛋白,这些提取物的凋亡能力得以恢复。这些结果直接证明crk参与凋亡信号传导。