Fujii Hideaki, Hirose Tetsuro, Oe Shoshiro, Yasuchika Kentaro, Azuma Hisaya, Fujikawa Takahisa, Nagao Masaya, Yamaoka Yoshio
Department of Gastroenterological Surgery, Kyoto University Graduate School of Medicine, 54, Kawara-cho, Shogoin, Sakyo-ku, Kyoto 606-8507, Japan.
J Hepatol. 2002 May;36(5):653-9. doi: 10.1016/s0168-8278(02)00043-0.
BACKGROUND/AIMS: We examined whether bone marrow (BM) cells can commit to liver-consisting cells during liver regeneration after partial hepatectomy, using mice transplanted with green fluorescent protein (GFP) positive BM from GFP transgenic mice.
Partial hepatectomy or sham operation was performed. Lineage marker analysis of GFP positive liver cells was by immunostaining and flow cytometry. DiI-labeled acetylated low-density lipoprotein uptake or microsphere phagocytosis was examined in vitro. Lineage marker expression in BM and peripheral blood (PB) cells, and the vascular endothelial growth factor (VEGF) concentration in the liver were also examined.
In hepatectomized mice, significantly more GFP positive cells participated in liver sinusoid than in sham-operated mice, expressing CD31 but not albumin. The percentage of cells that incorporated acetylated low-density lipoprotein but not microspheres was 69.5+/-3.4%, while 28.3+/-2.6% incorporated both, revealing sinusoidal endothelial and Kupffer cells, respectively. Increased expression of the CD31 and CD16/CD32 on GFP positive liver cells was also detected. The elevation of the VEGF concentration during liver regeneration and the increase in the CD34 and Flk-1 expression in the liver, BM, and PB cells suggested endothelial progenitor cell mobilization.
GFP cell-marking provided direct evidence of the BM cells participation in liver regeneration after hepatectomy, where the majority was committed to sinusoidal endothelial cells probably through endothelial progenitor cell mobilization.
背景/目的:我们利用移植了绿色荧光蛋白(GFP)转基因小鼠的GFP阳性骨髓(BM)细胞的小鼠,研究了部分肝切除术后肝脏再生过程中BM细胞是否能分化为肝脏组成细胞。
进行部分肝切除术或假手术。通过免疫染色和流式细胞术对GFP阳性肝细胞进行谱系标记分析。在体外检测DiI标记的乙酰化低密度脂蛋白摄取或微球吞噬作用。还检测了BM和外周血(PB)细胞中的谱系标记表达以及肝脏中的血管内皮生长因子(VEGF)浓度。
在肝切除小鼠中,参与肝血窦的GFP阳性细胞明显多于假手术小鼠,这些细胞表达CD31但不表达白蛋白。摄取乙酰化低密度脂蛋白但不摄取微球的细胞百分比为69.5±3.4%,而同时摄取两者的细胞百分比为28.3±2.6%,分别揭示了肝血窦内皮细胞和库普弗细胞。还检测到GFP阳性肝细胞上CD31和CD16/CD32表达增加。肝脏再生过程中VEGF浓度的升高以及肝脏、BM和PB细胞中CD34和Flk-1表达的增加提示内皮祖细胞动员。
GFP细胞标记为肝切除术后BM细胞参与肝脏再生提供了直接证据,其中大多数可能通过内皮祖细胞动员分化为肝血窦内皮细胞。