Sunamoto M, Kuze K, Tsuji H, Ohishi N, Yagi K, Nagata K, Kita T, Doi T
Department of Clinical Bio-Regulatory Science, Faculty of Medicine, Kyoto University, Japan.
Lab Invest. 1998 Aug;78(8):967-72.
Heat shock protein 47 (HSP47) is a collagen-specific molecular chaperone that has been shown to play a major role during the biosynthesis and secretion of procollagen molecules. The expression of HSP47 has been reported to increase in parallel with the expression of collagens during the progression of various fibrosis models. However, it remains unclear whether an inhibition of HSP47 overexpression would suppress collagen accumulation and thus reduce the progression of fibrotic diseases. In this study, we attempted to attenuate glomerular collagen accumulation by inhibiting the overexpression of HSP47 with antisense oligodeoxynucleotides in an experimental glomerulonephritis model induced by anti-Thy-1 antibodies. The administration of antisense oligodeoxynucleotides against HSP47 at the induction of the glomerular disease markedly suppressed the increased production of collagens and attenuated the histologic manifestations of the disease. These results provide direct evidence of a pivotal role for HSP47 in the pathogenesis of glomerulonephritis.
热休克蛋白47(HSP47)是一种胶原蛋白特异性分子伴侣,已被证明在原胶原分子的生物合成和分泌过程中起主要作用。据报道,在各种纤维化模型的进展过程中,HSP47的表达与胶原蛋白的表达平行增加。然而,HSP47过表达的抑制是否会抑制胶原蛋白的积累从而减少纤维化疾病的进展仍不清楚。在本研究中,我们试图在抗Thy-1抗体诱导的实验性肾小球肾炎模型中,通过用反义寡脱氧核苷酸抑制HSP47的过表达来减轻肾小球胶原蛋白的积累。在肾小球疾病诱导时给予针对HSP47的反义寡脱氧核苷酸,显著抑制了胶原蛋白产生的增加,并减轻了疾病的组织学表现。这些结果提供了直接证据,证明HSP47在肾小球肾炎发病机制中起关键作用。