Zhou M, Wu X, Ginsberg H N
Department of Medicine, College of Physicians and Surgeons of Columbia University, New York, New York 10032, USA.
J Biol Chem. 1996 Oct 4;271(40):24769-75. doi: 10.1074/jbc.271.40.24769.
Heat shock protein 72/73 (Hsp70) is a cytosolic molecular chaperone that carries out fundamental roles under both normal and stress situations. There is great interest in delineating the mechanisms whereby Hsp70 levels are regulated. We observed that N-acetyl-leucyl-leucyl-norleucinal (ALLN), a synthetic aldehydic tripeptide that inhibits proteasomes, markedly induced Hsp70 levels (up to 30-fold above base line in HepG2 cells and human endothelial cells). Induction of Hsp70 by ALLN was dose-dependent and not related to cell toxicity. ALLN selectively increased Hsp70 levels without affecting Hsp25, Hsp27, Hsp60, Hsp86, Hsp90, Hsp104, or Bip (immunoglobulin heavy chain binding protein) in HepG2 cells. ALLN induced Hsp70 not only by stabilizing the protein but also by dramatically increasing its synthesis. The modulation of Hsp70 synthesis by ALLN resulted from a rapid and marked increase in transcription of the hsp72 gene, since the induction of hsp72 mRNA was blocked in cells co-treated with actinomycin D. hsp72 mRNA levels were affected in a time-dependent manner by exposure to ALLN; significant elevations occurred within 60 min of treatment, and a decline to background levels was observed by 7 h of recovery. The ALLN-induced increase in hsp72 gene expression was associated with trimerization of the heat shock transcriptional factor (HSF1). ALLN did not affect the steady-state level of HSF1 protein. The effects of ALLN appeared to require de novo protein synthesis, since the induction of both HSF1 trimerization and hsp72 transcription was blocked by co-treatment with cycloheximide. When we tested a series of protease inhibitors, only the related aldehydic tripeptides, N-acetyl-leucyl-leucyl-methioninal and the proteasome inhibitor, Cbz-leucyl-leucyl-leucinal, induced Hsp70 levels. The specific proteasome inhibitor, lactacystin, which has a different structure, also induced Hsp70 levels. Overall, our results suggest that a rapidly turning over protein that is normally degraded by proteasomes may be involved in the regulation of Hsp70 synthesis via effects on the hsp70 transcriptional factor, HSF1.
热休克蛋白72/73(Hsp70)是一种胞质分子伴侣,在正常和应激情况下均发挥着重要作用。人们对阐明Hsp70水平的调控机制有着浓厚兴趣。我们观察到,N - 乙酰 - 亮氨酰 - 亮氨酰 - 正亮氨酸(ALLN),一种抑制蛋白酶体的合成醛三肽,能显著诱导Hsp70水平(在HepG2细胞和人内皮细胞中比基线水平高出30倍)。ALLN对Hsp70的诱导呈剂量依赖性,且与细胞毒性无关。ALLN能选择性地提高Hsp70水平,而不影响HepG2细胞中的Hsp25、Hsp27、Hsp60、Hsp86、Hsp90、Hsp104或Bip(免疫球蛋白重链结合蛋白)。ALLN诱导Hsp70不仅是通过稳定该蛋白,还通过显著增加其合成。ALLN对Hsp70合成的调节是由于hsp72基因转录的快速且显著增加,因为在与放线菌素D共同处理的细胞中,hsp72 mRNA的诱导被阻断。hsp72 mRNA水平受ALLN暴露的时间依赖性影响;处理后60分钟内出现显著升高,恢复7小时后观察到降至背景水平。ALLN诱导的hsp72基因表达增加与热休克转录因子(HSF1)的三聚化有关。ALLN不影响HSF1蛋白的稳态水平。ALLN的作用似乎需要从头合成蛋白质,因为与环己酰亚胺共同处理可阻断HSF1三聚化和hsp72转录的诱导。当我们测试一系列蛋白酶抑制剂时,只有相关的醛三肽N - 乙酰 - 亮氨酰 - 亮氨酰 - 甲硫氨酸和蛋白酶体抑制剂Cbz - 亮氨酰 - 亮氨酰 - 亮氨酸能诱导Hsp70水平。结构不同的特异性蛋白酶体抑制剂乳胞素也能诱导Hsp70水平。总体而言,我们的结果表明,一种通常被蛋白酶体降解的快速周转蛋白可能通过影响hsp70转录因子HSF1参与Hsp70合成的调控。