Park Hyung Sub, Choi Geum Hee, Hahn Soli, Yoo Young Sun, Jung In Mok, Lee Taeseung
Department of Surgery, Seoul National University College of Medicine, Seoul ; Department of Surgery, Seoul National University Bundang Hospital, Seongnam.
Department of Surgery, Seoul National University Bundang Hospital, Seongnam.
Vasc Specialist Int. 2014 Mar;30(1):11-8. doi: 10.5758/vsi.2014.30.1.11. Epub 2014 Mar 30.
To examine the fate of muscle-derived stem cells (MDSC) after injection into different host conditions and provide an insight for their mechanism of action.
MDSCs differentiated in vitro towards the endothelial lineage and transfected with lentivirus tagged with green fluorescent protein (GFP) were injected into two animal models mimicking vascular diseases: hindlimb ischemia and carotid injury models. Injected cells were tracked at the site of injection and in remote organs by harvesting the respective tissues at different time intervals and performing immunofluorescent histological analyses. Stem cell survival was quantified at the site of injection for up to 4 weeks.
MDSCs were successfully tagged with fluorescent material GFP and showed successful implantation into the respective injection sites. These cells showed a higher affinity to implant in blood vessel walls as shown by double fluorescent co-stain with CD31. Quantification of stem cell survival showed a timede pendent decrease from day 3 to 4 weeks (survival rate normalized against day 3 was 72.0% at 1 week, 26.8% at 2 weeks and 2.4% at 4 weeks). Stem cells were also found in distant organs, especially the kidneys and liver, which survived up to 4 weeks.
MDSCs were successfully tracked in different vascular disease models, and their fate was assessed in terms of cell survival and distribution. Better understanding of the donor cell properties, including their interaction with the host conditions and their mechanism of action, are needed to enhance cell survival and achieve improved outcomes.
研究肌肉衍生干细胞(MDSC)注射到不同宿主条件后的命运,并深入了解其作用机制。
将在体外向内皮谱系分化并转染绿色荧光蛋白(GFP)标记慢病毒的MDSC注射到两种模拟血管疾病的动物模型中:后肢缺血模型和颈动脉损伤模型。通过在不同时间间隔采集相应组织并进行免疫荧光组织学分析,在注射部位和远处器官追踪注射的细胞。在注射部位对干细胞存活情况进行长达4周的定量分析。
MDSC成功用荧光物质GFP标记,并成功植入相应的注射部位。如与CD31的双重荧光共染色所示,这些细胞在血管壁中的植入亲和力更高。干细胞存活情况的定量分析显示,从第3天到第4周呈时间依赖性下降(相对于第3天的存活率,第1周为72.0%,第2周为26.8%,第4周为2.4%)。在远处器官,尤其是肾脏和肝脏中也发现了干细胞,它们存活长达4周。
在不同的血管疾病模型中成功追踪到了MDSC,并从细胞存活和分布方面评估了它们的命运。需要更好地了解供体细胞特性,包括它们与宿主条件的相互作用及其作用机制,以提高细胞存活率并取得更好的结果。