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骨化三醇通过调节凋亡相关基因抑制大鼠同种异体移植肝中的肝细胞凋亡。

Calcitriol inhibits hepatocyte apoptosis in rat allograft by regulating apoptosis-associated genes.

作者信息

Zhang Aibin, Wang Yan, Xie Haiyang, Zheng Shusen

机构信息

Key Lab of Combined Multi-Organ Transplantation, Chinese Ministry of Public Health, First Affiliated Hospital, Zhejiang University School of Medicine, 79 Qingchun Road, Hangzhou 310003, China.

出版信息

Int Immunopharmacol. 2007 Aug;7(8):1122-8. doi: 10.1016/j.intimp.2007.03.007. Epub 2007 Apr 25.

Abstract

Calcitriol, the active form of vitamin D, exerts important immunoregulatory effects. After rat liver allografting, calcitriol suppresses acute rejection. The aim of this study was to investigate whether calcitriol regulates hepatocyte apoptosis, in parallel with its inhibition of acute rejection in rat liver allografts. Liver allografts were transplanted in a high responder strain combination (SD to Wistar rats) and calcitriol was administered to the recipients, while control recipients received no immunosuppressant. Graft specimens were harvested on postoperative days 1, 3, 5 and 7 for histological analysis and protein assay. Hepatocyte apoptosis was assessed by the TUNEL method. Levels of intragraft Bcl-2, Bcl-xL, Bax, TNF-alpha and IFN-gamma proteins were measured by Western blot analysis. Expression of Fas, Fas ligand and caspase-3 was determined by immunohistochemical analysis. Calcitriol markedly inhibited hepatocyte apoptosis. In the calcitriol-treated allografts, Bcl-2 and Bcl-xL levels increased while Bax and caspase-3 levels significantly decreased. The expression of Fas ligand was clearly reduced while Fas remained unchanged. TNF-alpha and IFN-gamma proteins were also significantly decreased in the presence of calcitriol. These results show that calcitriol acts as a promoter of the anti-apoptosis genes Bcl-2 and Bcl-xL and an inhibitor of the pro-apoptosis genes Bax and caspase-3. These effects may be related to its suppression of the Fas/Fas ligand pathway and its inhibition of cytotoxic T lymphocyte products.

摘要

骨化三醇,即维生素D的活性形式,具有重要的免疫调节作用。大鼠肝脏同种异体移植后,骨化三醇可抑制急性排斥反应。本研究旨在探讨骨化三醇在抑制大鼠肝脏同种异体移植急性排斥反应的同时,是否对肝细胞凋亡具有调节作用。将肝脏同种异体移植于高反应性品系组合(从SD大鼠到Wistar大鼠)中,并给受体大鼠施用骨化三醇,而对照受体大鼠不接受免疫抑制剂。在术后第1、3、5和7天采集移植组织标本进行组织学分析和蛋白质检测。采用TUNEL法评估肝细胞凋亡情况。通过蛋白质印迹分析测定移植组织内Bcl-2、Bcl-xL、Bax、肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)蛋白的水平。通过免疫组织化学分析确定Fas、Fas配体和半胱天冬酶-3的表达。骨化三醇显著抑制肝细胞凋亡。在经骨化三醇处理的同种异体移植组织中,Bcl-2和Bcl-xL水平升高,而Bax和半胱天冬酶-3水平显著降低。Fas配体的表达明显降低,而Fas保持不变。在骨化三醇存在的情况下,TNF-α和IFN-γ蛋白也显著降低。这些结果表明,骨化三醇可作为抗凋亡基因Bcl-2和Bcl-xL的促进剂以及促凋亡基因Bax和半胱天冬酶-3的抑制剂。这些作用可能与其对Fas/Fas配体途径的抑制以及对细胞毒性T淋巴细胞产物的抑制有关。

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