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热休克蛋白、蛋白水解酶和磷酸酶在大鼠肝再生中的含量和活性变化
作者姓名:Xu CS  Xia M  Lu AL  Li XY  Li YH  Zhao XY  Hu YH
作者单位::徐存拴 夏 民 卢爱灵 李效阳 李永辉 赵绪永 胡轶红 河南师范大学生命科学学院, 新乡 453002
基金项目:河南省生物工程重点实验室资助
摘    要:本文以2/3肝切除(partial hepatectomy,PH)大鼠为模型,探讨了PH后酸性和碱性磷酸酶(acid and alkaline phosphatases,ACP和AKP),构成性热休克蛋白70/诱导性热休克蛋白68(HSC7/HSP68),酸性和中性蛋白水解酶在肝再生期间(0-144h)的动态变化。结果显示,在肝切除后的肝再生期间;(1)ACP和AKP均出现两个活性高峰(4和48h

关 键 词:肝再生  热休蛋白  蛋白水解酶  复性电泳

Changes in the content and activity of HSC70/HSP68, proteinases and phosphatases during liver regeneration
Xu CS,Xia M,Lu AL,Li XY,Li YH,Zhao XY,Hu YH.Changes in the content and activity of HSC70/HSP68, proteinases and phosphatases during liver regeneration[J].Acta Physiologica Sinica,1999,51(5):548-556.
Authors:Xu C S  Xia M  Lu A L  Li X Y  Li Y H  Zhao X Y  Hu Y H
Institution:College of Life Science, Henan Normal University, Xinxiang 453002.
Abstract:This article reports changes in acid and alkaline phosphatases (ACP and AKP),conshtutive heat shock protein 70/induced heat shock protein 68 (HSC70/HSP68) andacid and neutal proteinases ddring liver regeneration (0 ~ 144 h) after 2/3 hepatectomy(pwhal hepatectomy, PH). Both ACP and AKP had two achve peaks at 4 and 48 h, 16and 96 h, respectively, which were followed by sighficant decrease. The content ofHSC70/HSP68 also showed two Peaks (16 and 96 h), of which the content after thesecond Peak decnaed more obviously than after the first peak. Moreover a 90 kD neutalproteinase was induced at the time from 2 to 6 h and a 27 kD acid proteinase was inducedat 36 h. The results suggest that the ACP and the 90 kD neuhal proteinase rnayparticipate in activahng hepatocytes from G0-Phase into G1-phase, and are and HSC70/HSP68 may play a role ndnly in DNA synthesis, cellular metabolism and proliferation.Fdriermore 27 kD acid proteinase may be involved in re-differentiation of hepatocytesand reconsmichon of liver tissue.
Keywords:liver regeneration  constitutive heat shock protein 70/induced heat shock protein 68(HSC70/HSP68 )  proteinases  acid phosphatase (ACP)  alkaline phosphatase(AKP)  non-denatured electrophoresis
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