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肝切除术后肝再生过程中免疫抑制剂对肝细胞增殖和凋亡的影响——分子研究

Effect of the immunosuppressants on hepatocyte cells proliferation and apoptosis during liver regeneration after hepatectomy - molecular studies.

作者信息

Tannuri Uenis, Tannuri Ana C A, Coelho Maria C A, Mello Evandro S, dos Santos Aparecida S R

机构信息

University of São Paulo Medical School, São Paulo, Brazil.

出版信息

Pediatr Transplant. 2008 Feb;12(1):73-79. doi: 10.1111/j.1399-3046.2007.00801.x.

Abstract

The regeneration and remodeling of the transplanted liver is the result of hepatocyte proliferation and apoptosis (programmed cell death). The purpose of this study was to verify the influence of immunosuppressants on the expression levels of genes: IL-6 (regulator of hepatocyte proliferation), pro-apoptotic (Bak and Bax) and anti-apoptotic (Bcl-Xl and Bcl-2). 36 newborn suckling rats (age 5-7 days, weight 6-10 g) were divided into four groups: hepatectomy, hepatectomy plus methylprednisolone, hepatectomy plus CsA and hepatectomy plus Tac. The same experiments were performed in 24 weaning rats (age 21-23 days, weight 30-50 g). The animals were killed one day after the hepatectomy and the remnant livers were analyzed. The livers of all animals exhibited histological changes of liver regeneration. The immunosuppressants did not promote any alteration on IL-6 gene expression levels. Methylprednisolone and CsA increased the expression levels of Bak gene in newborn rats. However, methylprednisolone and Tac promoted increased expression levels of Bcl-2 in all groups. We hypothesize that these effects explain the efficacy of these drugs on the treatment of acute and chronic liver rejection as the expression of Bcl-2 in cholangiocytes is decreased as a consequence of bile duct lesions

摘要

移植肝脏的再生和重塑是肝细胞增殖和凋亡(程序性细胞死亡)的结果。本研究的目的是验证免疫抑制剂对以下基因表达水平的影响:IL-6(肝细胞增殖调节剂)、促凋亡基因(Bak和Bax)以及抗凋亡基因(Bcl-Xl和Bcl-2)。将36只新生乳鼠(年龄5 - 7天,体重6 - 10克)分为四组:肝切除组、肝切除加甲基强的松龙组、肝切除加环孢素A组和肝切除加他克莫司组。对24只断乳大鼠(年龄21 - 23天,体重30 - 50克)进行了相同实验。肝切除术后一天处死动物,并对残余肝脏进行分析。所有动物的肝脏均呈现出肝脏再生的组织学变化。免疫抑制剂未对IL-6基因表达水平产生任何改变。甲基强的松龙和环孢素A增加了新生大鼠Bak基因的表达水平。然而,甲基强的松龙和他克莫司在所有组中均促进了Bcl-2表达水平的升高。我们推测,这些作用解释了这些药物在治疗急性和慢性肝排斥反应方面的疗效,因为胆管病变会导致胆管细胞中Bcl-2的表达降低

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