• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肝细胞和肝血窦细胞胶原酶在实验性肝硬变可逆性中的作用

Collagenase of hepatocytes and sinusoidal liver cells in the reversibility of experimental cirrhosis of the liver.

作者信息

Montfort I, Pérez-Tamayo R, Alvizouri A M, Tello E

机构信息

Sub-Division de Medicina Experimental, Facultad de Medicina, Universidad Nacional Autónoma de México, México City.

出版信息

Virchows Arch B Cell Pathol Incl Mol Pathol. 1990;59(5):281-9. doi: 10.1007/BF02899415.

DOI:10.1007/BF02899415
PMID:1980558
Abstract

In order to explore the cellular source(s) and the behaviour of the collagenolytic activity previously described in rat liver homogenates, in the reversibility of experimental cirrhosis of the liver, enriched suspensions of hepatocytes and of sinusoidal liver cells were obtained by a procedure which employs low EDTA concentrations and no bacterial collagenase. Cell suspensions were prepared from three different groups of animals: 1) normal controls, 2) rats with CCl4-induced cirrhosis of the liver, and 3) rats with swine serum-induced cirrhosis of the liver. Animals were sacrificed in each group upon completion of treatment and also after 3, 6 and 12 months. In each liver wet weight and collagen concentration were determined, and collagenolytic activity of both enriched cell suspensions was measured separately. In addition, histological studies of liver tissue and ultrastructural examination of cell suspensions were performed by standard procedures. Enriched suspensions of both normal hepatocytes and sinusoidal liver cells display Ca2(+)-dependent collagenolytic activities. Both cell suspensions obtained from each of the two types of cirrhotic livers show normal or slightly increased average levels of collagenase activity at the time of treatment discontinuation, when average liver collagen content ranges from 6 to 10-fold over normal, suggesting that the normal collagenase/collagen ratio is disturbed and that collagenolytic activity is deeply decreased in relation to the actual liver collagen load.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了探究先前在大鼠肝脏匀浆中所描述的胶原分解活性的细胞来源及其行为,以及实验性肝硬变的可逆性,我们采用低乙二胺四乙酸(EDTA)浓度且不使用细菌胶原酶的方法,获得了富含肝细胞和肝血窦细胞的悬浮液。细胞悬浮液取自三组不同的动物:1)正常对照组;2)四氯化碳诱导的肝硬变大鼠;3)猪血清诱导的肝硬变大鼠。每组动物在治疗结束时以及治疗后3个月、6个月和12个月时处死。测定每个肝脏的湿重和胶原浓度,并分别测量两种富含细胞悬浮液的胶原分解活性。此外,通过标准程序对肝组织进行组织学研究,并对细胞悬浮液进行超微结构检查。正常肝细胞和肝血窦细胞的富含悬浮液均表现出钙离子依赖性胶原分解活性。从两种类型的肝硬化肝脏中获取的两种细胞悬浮液,在停止治疗时,其胶原酶活性平均水平正常或略有升高,此时肝脏胶原平均含量比正常高6至10倍,这表明正常的胶原酶/胶原比例受到干扰,并且相对于实际的肝脏胶原负荷,胶原分解活性大幅降低。(摘要截断于250字)

相似文献

1
Collagenase of hepatocytes and sinusoidal liver cells in the reversibility of experimental cirrhosis of the liver.肝细胞和肝血窦细胞胶原酶在实验性肝硬变可逆性中的作用
Virchows Arch B Cell Pathol Incl Mol Pathol. 1990;59(5):281-9. doi: 10.1007/BF02899415.
2
Collagenolytic activity in experimental cirrhosis of the liver.实验性肝硬化中的胶原酶活性
Exp Mol Pathol. 1987 Dec;47(3):300-8. doi: 10.1016/0014-4800(87)90015-3.
3
Collagenase in experimental carbon tetrachloride cirrhosis of the liver.实验性四氯化碳性肝硬变中的胶原酶
Am J Pathol. 1978 Aug;92(2):411-20.
4
Collagenase and collagenolytic cathepsin in normal and fibrotic rat liver.正常和纤维化大鼠肝脏中的胶原酶和胶原分解组织蛋白酶
J Biochem. 1990 Aug;108(2):241-4. doi: 10.1093/oxfordjournals.jbchem.a123187.
5
Anti-fibrotic effect of malotilate on liver fibrosis induced by carbon tetrachloride in rats.马洛替酯对四氯化碳诱导的大鼠肝纤维化的抗纤维化作用。
Jpn J Exp Med. 1986 Oct;56(5):235-45.
6
Different appearance of hepatic collagenase and lysosomal enzymes in recovery of experimental hepatic fibrosis.实验性肝纤维化恢复过程中肝胶原酶和溶酶体酶的不同表现
Biochem Exp Biol. 1978;14(3):191-201.
7
Fibrogenic and collagenolytic activity in carbon-tetrachloride-injured rats: beneficial effects of zinc administration.四氯化碳损伤大鼠的纤维化和胶原溶解活性:锌给药的有益作用。
J Hepatol. 1994 Sep;21(3):292-8. doi: 10.1016/s0168-8278(05)80304-6.
8
Stimulation of interstitial collagenase in co-cultures of rat hepatocytes and sinusoidal cells.大鼠肝细胞与窦状隙细胞共培养体系中间质胶原酶的刺激作用。
Gastroenterology. 1986 Apr;90(4):829-36. doi: 10.1016/0016-5085(86)90858-9.
9
In micronodular cirrhosis, hepatocytes retain a normal C-25 hydroxylation capacity toward vitamin D3: a study using the rat carbon tetrachloride-induced cirrhotic model.在微结节性肝硬化中,肝细胞对维生素D3保持正常的C-25羟化能力:一项使用大鼠四氯化碳诱导肝硬化模型的研究。
Hepatology. 1991 Mar;13(3):489-99. doi: 10.1002/hep.1840130317.
10
Adenosine reverses a preestablished CCl4-induced micronodular cirrhosis through enhancing collagenolytic activity and stimulating hepatocyte cell proliferation in rats.腺苷通过增强胶原分解活性和刺激大鼠肝细胞增殖来逆转预先建立的四氯化碳诱导的小结节性肝硬化。
Hepatology. 2001 Oct;34(4 Pt 1):677-87. doi: 10.1053/jhep.2001.27949.

引用本文的文献

1
Modeling the Effect of the Metastatic Microenvironment on Phenotypes Conferred by Estrogen Receptor Mutations Using a Human Liver Microphysiological System.使用人类肝微生理系统对雌激素受体突变赋予的表型进行转移微环境效应建模。
Sci Rep. 2019 Jun 6;9(1):8341. doi: 10.1038/s41598-019-44756-5.
2
Reciprocal modulation of matrix metalloproteinase-13 and type I collagen genes in rat hepatic stellate cells.大鼠肝星状细胞中基质金属蛋白酶-13与I型胶原基因的相互调节
Am J Pathol. 2003 Jun;162(6):1771-80. doi: 10.1016/S0002-9440(10)64312-X.
3
Mechanisms of spontaneous resolution of rat liver fibrosis. Hepatic stellate cell apoptosis and reduced hepatic expression of metalloproteinase inhibitors.
大鼠肝纤维化自发消退的机制。肝星状细胞凋亡及金属蛋白酶抑制剂肝表达降低。
J Clin Invest. 1998 Aug 1;102(3):538-49. doi: 10.1172/JCI1018.
4
Localization of messenger RNA for tissue inhibitor of metalloproteinases-1 and type IV collagenases/gelatinases in monkey hepatocellular carcinomas.金属蛋白酶组织抑制剂-1和IV型胶原酶/明胶酶信使核糖核酸在猴肝细胞癌中的定位
Clin Exp Metastasis. 1995 Sep;13(5):381-8. doi: 10.1007/BF00121914.
5
Human hepatic lipocytes synthesize tissue inhibitor of metalloproteinases-1. Implications for regulation of matrix degradation in liver.人肝脂肪细胞合成金属蛋白酶组织抑制剂-1。对肝脏基质降解调节的意义。
J Clin Invest. 1992 Jul;90(1):282-7. doi: 10.1172/JCI115850.