Faherty C J, Xanthoudakis S, Smeyne R J
Department of Developmental Neurobiology, St. Jude Children's Research Hospital, 332 North Lauderdale, Memphis, TN 38105, USA.
Brain Res Mol Brain Res. 1999 Jun 18;70(1):159-63. doi: 10.1016/s0169-328x(99)00143-6.
In this study, we examined the levels of activated caspase-3 in the kainic acid (KA) model of hippocampal degeneration in both sensitive (FVB/N) and resistant (129/SvEMS) strains of mice. At 30 h, 2 and 4 days following KA administration, animals were sacrificed and brains examined for pyknosis, TUNEL labeling, and activated caspase-3 immunoreactivity. Catalytically active caspase-3 was first detected 30 h following KA treatment in the sensitive, FVB/N strain. This was 18 h before the appearance of pyknosis or TUNEL labeling. The expression of activated caspase-3 continues up to 4 days post-injection. No activated caspase-3 immunoreactivity was detected in the resistant, 129/SvEMS strain, neither was there evidence of pyknosis or TUNEL staining. This suggests that activation of caspase-3 is a necessary component of KA-induced cell death.
在本研究中,我们检测了在海马退变的红藻氨酸(KA)模型中,敏感型(FVB/N)和抗性型(129/SvEMS)小鼠品系中活化的半胱天冬酶-3的水平。在给予KA后的30小时、2天和4天,处死动物并检查大脑的核固缩、TUNEL标记和活化的半胱天冬酶-3免疫反应性。在敏感的FVB/N品系中,KA处理后30小时首次检测到具有催化活性的半胱天冬酶-3。这比核固缩或TUNEL标记出现早18小时。活化的半胱天冬酶-3的表达持续至注射后4天。在抗性的129/SvEMS品系中未检测到活化的半胱天冬酶-3免疫反应性,也没有核固缩或TUNEL染色的证据。这表明半胱天冬酶-3的激活是KA诱导细胞死亡的必要组成部分。