Vilalta Marta, Dégano Irene R, Bagó Juli, Gould David, Santos Mònica, García-Arranz Mariano, Ayats Ramon, Fuster Carme, Chernajovsky Yuti, García-Olmo Damián, Rubio Nuria, Blanco Jerónimo
Centre d'investigació Cardiovascular (CSIC-ICCC), CIBER de Bioingenieria, Biomateriales y Nanomedicine (CIBER-BBN), Zaragoza, Spain.
Stem Cells Dev. 2008 Oct;17(5):993-1003. doi: 10.1089/scd.2007.0201.
Cultivated murine bone marrow mesenchymal stem cells (MSCs) frequently accumulate chromosome abnormalities, become oncogenically transformed, and generate sarcomas when transplanted in mice. Although human MSCs appear to be more resistant, oncogenic transformation has also been observed in MSCs cultivated past the senescence phase. Cell therapy for tissue regeneration using human autologous MSCs requires transplantation of cells previously expanded in vitro. Thus, an important concern is to determine if oncogenic transformation is a necessary outcome of the expansion procedures. We have analyzed the proliferation capacity, organ colonization, and oncogenicity of enhanced green fluorescent protein and luciferase-labeled human adipose tissue-derived mesenchymal stem cells (hAMSCs), implanted in immunocompromised mice during a prolonged time period (8 months) using a non-invasive bioluminescence imaging procedure. Our data indicates that the liver was the preferred target organ for colonization by intramuscular or intravenous implantation of hAMSCs. The implanted cells tended to maintain a steady state, population did not proliferate rapidly after implantation, and no detectable chromosomal abnormalities nor tumors formed during the 8 months of residence in the host's tissues. It would appear that hAMSCs, contrary to their murine correlatives, could be safe candidates for autologous cell therapy procedures since in our experiments they show undetectable predisposition to oncogenic transformation after cultivation in vitro and implantation in mice.
培养的小鼠骨髓间充质干细胞(MSC)在移植到小鼠体内时经常会积累染色体异常,发生致癌转化并产生肉瘤。尽管人MSC似乎更具抗性,但在衰老期之后培养的MSC中也观察到了致癌转化。使用人自体MSC进行组织再生的细胞疗法需要移植先前在体外扩增的细胞。因此,一个重要的问题是确定致癌转化是否是扩增过程的必然结果。我们使用非侵入性生物发光成像程序,分析了增强型绿色荧光蛋白和荧光素酶标记的人脂肪组织来源的间充质干细胞(hAMSC)在免疫缺陷小鼠体内长时间(8个月)植入后的增殖能力、器官定植和致癌性。我们的数据表明,通过肌肉内或静脉内植入hAMSC,肝脏是定植的首选靶器官。植入的细胞倾向于维持稳定状态,植入后细胞群体不会快速增殖,并且在宿主组织中驻留的8个月内未形成可检测到的染色体异常或肿瘤。与它们的小鼠同类细胞相反,hAMSC似乎可能是自体细胞治疗程序的安全候选者,因为在我们的实验中,它们在体外培养和植入小鼠后未显示出可检测到的致癌转化倾向。