Makino Hironobu, Shimizu Hiroaki, Ito Hiroshi, Kimura Fumio, Ambiru Satoshi, Togawa Akira, Ohtsuka Masayuki, Yoshidome Hiroyuki, Kato Atsushi, Yoshitomi Hideyuki, Sawada Shigeaki, Miyazaki Masaru
Department of General Surgery, Graduate School of Medicine, Chiba University, 1-8-1 Inohana, Chiba 260-0856, Japan.
World J Gastroenterol. 2006 Apr 7;12(13):2053-9. doi: 10.3748/wjg.v12.i13.2053.
To study the effects of obstructive jaundice on liver regeneration after partial hepatectomy.
Hepatocyte growth factor (HGF), its receptor, c-Met, vascular endothelial growth factor (VEGF) and transforming growth factor-beta1 (TGF-beta1) mRNA expression in both liver tissue and isolated liver cells were investigated after biliary obstruction (BO) by quantitative reverse-transcription polymerase chain reaction (RT-PCR) using a LightCycler. Immunohistochemical staining for desmin and alpha-smooth muscle actin (alpha-SMA) was also studied. Regenerating liver weight and proliferating cell nuclear antigen (PCNA) labeling index, and growth factor expression were then evaluated after 70% hepatectomy with concomitant internal biliary drainage in BO rats or sham-operated rats.
Hepatic TGF-beta1 mRNA levels increased significantly 14 days after BO, and further increased with duration of cholestasis. Meanwhile, HGF and VEGF tended to increase, but was not significant. In cell isolates, TGF-beta1 mRNA was found mainly in the hepatic stellate cell (HSC) fraction. Immunohistochemical studies revealed an increased number of HSCs (desmin-positive cells) and activated HSCs (alpha-SMA-positive cells) in portal areas after BO. In a hepatectomy model, liver regeneration was delayed in BO rats, as compared to sham-operated rats. TGF-beta1 mRNA was significantly up-regulated up to 48 h after hepatectomy, and the earlier HGF mRNA peak was lost in BO rats.
BO induces HSCs proliferation and activation, leading to up-regulation of TGF-beta1 mRNA and suppression of HGF mRNA in livers. These altered expression patterns may be strongly involved in delayed liver regeneration after hepatectomy with obstructive jaundice.
研究梗阻性黄疸对部分肝切除术后肝再生的影响。
采用LightCycler通过定量逆转录聚合酶链反应(RT-PCR),研究胆管梗阻(BO)后肝组织和分离的肝细胞中肝细胞生长因子(HGF)及其受体c-Met、血管内皮生长因子(VEGF)和转化生长因子-β1(TGF-β1)mRNA的表达。还研究了结蛋白和α-平滑肌肌动蛋白(α-SMA)的免疫组织化学染色。然后在BO大鼠或假手术大鼠中进行70%肝切除并伴有内胆管引流后,评估再生肝重量、增殖细胞核抗原(PCNA)标记指数和生长因子表达。
BO后14天肝组织TGF-β1 mRNA水平显著升高,并随胆汁淤积时间延长进一步升高。同时,HGF和VEGF有升高趋势,但不显著。在细胞分离物中,TGF-β1 mRNA主要存在于肝星状细胞(HSC)部分。免疫组织化学研究显示,BO后门管区HSC(结蛋白阳性细胞)数量增加,活化的HSC(α-SMA阳性细胞)数量增加。在肝切除模型中,与假手术大鼠相比,BO大鼠的肝再生延迟。肝切除术后48小时内TGF-β1 mRNA显著上调,且BO大鼠中较早出现的HGF mRNA峰值消失。
BO诱导HSC增殖和活化,导致肝脏中TGF-β1 mRNA上调和HGF mRNA抑制。这些改变的表达模式可能与梗阻性黄疸肝切除术后肝再生延迟密切相关。