Hayashi Yujiro, Tsuji Shingo, Tsujii Masahiko, Nishida Tsutomu, Ishii Shuji, Iijima Hideki, Nakamura Toru, Eguchi Hiroshi, Miyoshi Eiji, Hayashi Norio, Kawano Sunao
Department of Clinical Laboratory Science, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.
J Pharmacol Exp Ther. 2008 Aug;326(2):523-31. doi: 10.1124/jpet.108.137083. Epub 2008 Apr 30.
Mesenchymal stem cells (MSCs) are attractive cell sources in regenerative medicine. We examined the effects of topical MSCs implantation on an experimental model of inflammatory bowel disease. Putative MSCs, isolated from bone marrow aspirates of male rats by dish adherence and expanded in vitro, were characterized by flow cytometry, reverse transcription-polymerase chain reaction, enzyme-linked immunosorbent assay, and differentiation assays. Experimental colitis was induced by intraluminal instillation of 2,4,6-trinitrobonzene sulfonic acid (TNBS) in the colons of male rats. The putative MSCs and unselected fresh bone marrow cells were injected into the colonic submucosa surrounding the area exposed to TNBS. The healing process of the injury was examined macroscopically and immunohistologically. Multipotent MSCs positive for CD29 and CD90, and negative for CD31 and CD34, were implanted into colon tissue surrounding the lesion; a majority of the engrafted cells were positive for vimentin. The implantation significantly accelerated healing of the damaged mucosa compared with vehicle-injected controls. The MSCs expressed vascular endothelial growth factor (VEGF) and transforming growth factor (TGF)-beta1 in vitro and after the implantation. In conclusion, we found that MSCs were successfully topically implanted in the colon and that they were associated with accelerated healing of TNBS-induced colitis. The beneficial effects of the MSCs might be mediated, at least in part, by their ability to differentiate into colonic interstitial cells and by their ability to provide VEGF and TGF-beta1 to the injured area.
间充质干细胞(MSCs)是再生医学中颇具吸引力的细胞来源。我们研究了局部植入MSCs对炎症性肠病实验模型的影响。通过培养皿贴壁法从雄性大鼠骨髓抽吸物中分离出假定的MSCs,并在体外进行扩增,采用流式细胞术、逆转录-聚合酶链反应、酶联免疫吸附测定和分化测定对其进行表征。通过向雄性大鼠结肠腔内注入2,4,6-三硝基苯磺酸(TNBS)诱导实验性结肠炎。将假定的MSCs和未筛选的新鲜骨髓细胞注入暴露于TNBS区域周围的结肠黏膜下层。通过宏观和免疫组织学检查损伤的愈合过程。将CD29和CD90呈阳性、CD31和CD34呈阴性的多能MSCs植入病变周围的结肠组织;大多数植入细胞波形蛋白呈阳性。与注射赋形剂的对照组相比,植入显著加速了受损黏膜的愈合。MSCs在体外及植入后均表达血管内皮生长因子(VEGF)和转化生长因子(TGF)-β1。总之,我们发现MSCs成功地局部植入结肠,且与TNBS诱导的结肠炎加速愈合有关。MSCs的有益作用可能至少部分是通过其分化为结肠间质细胞的能力以及向损伤区域提供VEGF和TGF-β1的能力介导的。