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胆管细胞表面抗原HAM.4鉴定为二肽基肽酶IV(DPPIV)及其在大鼠部分肝切除术后肝再生中作用的表征

Identification of bile canalicular cell surface antigen HAM.4 as dipeptidyl peptidase IV (DPPIV) and characterization of its role in hepatic regeneration after partial hepatectomy in rats.

作者信息

Tsugiki M, Kobayashi Y, Kawasaki T, Yoshimi T

机构信息

Second Department of Internal Medicine, Hamamatsu University School of Medicine, Japan.

出版信息

Dig Dis Sci. 1998 Dec;43(12):2591-600. doi: 10.1023/a:1026678622356.

Abstract

Dipeptidyl peptidase IV (DPPIV) has been implicated in the control of cell growth and differentiation. A rat hepatocyte membrane antigen recognized by a monoclonal antibody (HAM.4) has now been shown to be identical to DPPIV by immunoblot analysis and amino acid sequencing. The amounts of DPPIV immunoreactive protein and enzymatic activity in serum increased in a manner independent of de novo protein synthesis, and without any biochemical or immunohistochemical changes in hepatic DPPIV, during liver regeneration after partial hepatectomy in rats. DPPIV purified from serum by HAM.4 antibody-based affinity chromatography lacked the NH2-terminal 36 amino acids of the membrane-bound enzyme, suggesting that proteolytic cleavage may mediate the release of DPPIV into serum. No significant differences in the restoration of liver mass or in hepatic DNA synthesis were apparent between DPPIV-deficient and normal rats after partial hepatectomy, suggesting that DPPIV may not be essential for hepatic regeneration.

摘要

二肽基肽酶IV(DPPIV)与细胞生长和分化的调控有关。一种被单克隆抗体(HAM.4)识别的大鼠肝细胞膜抗原,现已通过免疫印迹分析和氨基酸测序证明与DPPIV相同。在大鼠部分肝切除术后肝脏再生过程中,血清中DPPIV免疫反应性蛋白的量和酶活性以一种独立于从头蛋白质合成的方式增加,并且肝脏DPPIV没有任何生化或免疫组织化学变化。通过基于HAM.4抗体的亲和色谱从血清中纯化的DPPIV缺乏膜结合酶的NH2末端36个氨基酸,这表明蛋白水解切割可能介导DPPIV释放到血清中。部分肝切除术后,DPPIV缺陷型大鼠和正常大鼠在肝脏质量恢复或肝脏DNA合成方面没有明显差异,这表明DPPIV可能不是肝脏再生所必需的。

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