Hatayama T, Yamagishi N, Minobe E, Sakai K
Department of Biochemistry and Molecular Biology, Kyoto Pharmaceutical University, 5 Nakauchi-cho, Misasagi, Yamashina-ku, Kyoto, 607-8414, Japan.
Biochem Biophys Res Commun. 2001 Nov 2;288(3):528-34. doi: 10.1006/bbrc.2001.5802.
hsp105alpha is a stress protein characteristically highly expressed in the brain compared with other tissues in mammals. Here, to examine whether hsp105alpha plays a pivotal role in the nervous system, we tested the capability of hsp105alpha to protect against apoptosis in rat neuronal PC12 cells. Various stress treatments such as serum deprivation, heat shock, hydrogen peroxide, etoposide, and actinomycin D induced apoptosis in PC12 cells with characteristic shrinking of nuclei and chromatin. However, PC12 cells that constitutively overexpressed mouse hsp105alpha exhibited a strong protective effect against apoptosis induced by these stress treatments. Cleavage of poly(ADP-ribose) polymerase induced in PC12 cells by these treatments was inhibited in the constitutively overexpressed hsp105alpha cells. Furthermore, c-Jun N-terminal kinase (JNK) was activated in the cells treated with heat shock but not other treatments, and the heat-induced JNK activation was inhibited by the constitutive expression of hsp105alpha.Thus, hsp105alpha prevents not only heat-induced apoptosis by inhibiting JNK activation, but also prevents the apoptosis induced by other stressors through different pathways, and may play important roles in neuronal protection.
热休克蛋白105α(hsp105α)是一种应激蛋白,与哺乳动物的其他组织相比,其在大脑中具有特征性的高表达。在此,为了研究hsp105α是否在神经系统中起关键作用,我们测试了hsp105α保护大鼠神经元PC12细胞免受凋亡的能力。血清剥夺、热休克、过氧化氢、依托泊苷和放线菌素D等各种应激处理可诱导PC12细胞凋亡,并伴有细胞核和染色质的特征性收缩。然而,组成型过表达小鼠hsp105α的PC12细胞对这些应激处理诱导的凋亡表现出强大的保护作用。在组成型过表达hsp105α的细胞中,这些处理诱导的PC12细胞中聚(ADP - 核糖)聚合酶的切割受到抑制。此外,热休克处理的细胞中c - Jun氨基末端激酶(JNK)被激活,而其他处理则未激活,并且hsp105α的组成型表达抑制了热诱导的JNK激活。因此,hsp105α不仅通过抑制JNK激活来预防热诱导的凋亡,还通过不同途径预防其他应激源诱导的凋亡,并且可能在神经元保护中发挥重要作用。