Gernold M, Knauf U, Gaestel M, Stahl J, Kloetzel P M
Zentrum für Molekulare Biologie (ZMBH), Heidelberg, Germany.
Dev Genet. 1993;14(2):103-11. doi: 10.1002/dvg.1020140204.
We have investigated the developmental and tissue-specific distribution of the mouse small hsp25 by immunohistology using an antibody that specifically identifies hsp25. Our analysis shows that the relative amount of hsp25 increases during embryogenesis. Through days 13-20 of embryogenesis, hsp25 accumulation is predominant in the various muscle tissues, including the heart, the bladder, and the back muscles. hsp25 is detectable also in neurons of the spinal cord and the purkinje cells. Furthermore analysis of the closely related alpha, B-crystallin shows that in several tissues, including the bladder, the notochordal sheath and the eye lens both proteins are coexpressed. Our studies demonstrate that mammalian hsp25 accumulation is developmentally regulated during mouse embryogenesis and support the view of an important functional role of small heat shock proteins in normal cell metabolism.
我们使用一种能特异性识别热休克蛋白25(hsp25)的抗体,通过免疫组织学方法研究了小鼠小分子热休克蛋白25在发育过程中的表达及组织特异性分布。我们的分析表明,hsp25的相对含量在胚胎发育过程中增加。在胚胎发育的第13至20天,hsp25在包括心脏、膀胱和背部肌肉在内的各种肌肉组织中大量积累。在脊髓神经元和浦肯野细胞中也可检测到hsp25。此外,对密切相关的αB-晶状体蛋白的分析表明,在包括膀胱、脊索鞘和晶状体在内的几种组织中,这两种蛋白都共表达。我们的研究表明,在小鼠胚胎发育过程中,哺乳动物hsp25的积累受发育调控,并支持小分子热休克蛋白在正常细胞代谢中具有重要功能作用的观点。