Neame S J, Rubin L L, Philpott K L
Eisai London Research Laboratories, Bernard Katz Building, University College London, London WC1E 6BT, United Kingdom.
J Cell Biol. 1998 Sep 21;142(6):1583-93. doi: 10.1083/jcb.142.6.1583.
Cytochrome c has been shown to play a role in cell-free models of apoptosis. During NGF withdrawal-induced apoptosis of intact rat superior cervical ganglion (SCG) neurons, we observe the redistribution of cytochrome c from the mitochondria to the cytoplasm. This redistribution is not inhibited by the caspase inhibitor Z-Val-Ala-Asp-fluoromethylketone (ZVADfmk) but is blocked by either of the neuronal survival agents 8-(4-chlorophenylthio)adenosine 3':5'-cyclic monophosphate (CPT-cAMP) or cycloheximide. Moreover, microinjection of SCG neurons with antibody to cytochrome c blocks NGF withdrawal-induced apoptosis. However, microinjection of SCG neurons with cytochrome c does not alter the rate of apoptosis in either the presence or absence of NGF. These data suggest that cytochrome c is an intrinsic but not limiting component of the neuronal apoptotic pathway.
细胞色素c已被证明在无细胞凋亡模型中发挥作用。在神经生长因子(NGF)撤除诱导的完整大鼠颈上神经节(SCG)神经元凋亡过程中,我们观察到细胞色素c从线粒体重新分布到细胞质中。这种重新分布不受半胱天冬酶抑制剂Z-缬氨酰-丙氨酰-天冬氨酸-氟甲基酮(ZVADfmk)的抑制,但被两种神经存活剂之一8-(4-氯苯硫基)腺苷3':5'-环一磷酸(CPT-cAMP)或环己酰亚胺所阻断。此外,向SCG神经元显微注射抗细胞色素c抗体可阻断NGF撤除诱导的凋亡。然而,向SCG神经元显微注射细胞色素c在有或无NGF的情况下均不会改变凋亡速率。这些数据表明,细胞色素c是神经元凋亡途径的一个内在但非限制性成分。