CEINGE - Biotecnologie Avanzate, via Comunale Margherita 482, Napoli 80145, Italy.
BMC Cancer. 2010 Mar 30;10:120. doi: 10.1186/1471-2407-10-120.
Mollicutes contamination is recognized to be a critical issue for the cultivation of continuous cell lines. In this work we characterized the effect of Mycoplasma hyorhinis contamination on CD133 expression in human colon cancer cell lines.
MycoAlert and mycoplasma agar culture were used to detect mycoplasma contamination on GEO, SW480 and HT-29 cell lines. Restriction fragment length polymorphism assay was used to determine mycoplasma species. All cellular models were decontaminated by the use of a specific antibiotic panel (Enrofloxacin, Ciprofloxacin, BM Cyclin 1 and 2, Mycoplasma Removal Agent and MycoZap). The percentage of CD133 positive cells was analyzed by flow cytometry on GEO, SW480 and HT-29 cell lines, before and after Mycoplasma hyorhinis eradication.
Mycoplasma hyorhinis infected colon cancer cell lines showed an increased percentage of CD133+ cells as compared to the same cell lines rendered mycoplasma-free by effective exposure to antibiotic treatment. The percentage of CD133 positive cells increased again when mycoplasma negative cells were re-infected by Mycoplasma hyorhinis.
Mycoplasma hyorhinis infection has an important role on the quality of cultured human colon cancer cell lines giving a false positive increase of cancer stem cells fraction characterized by CD133 expression. Possible explanations are (i) the direct involvement of Mycoplasma on CD133 expression or (ii) the selective pressure on a subpopulation of cells characterized by constitutive CD133 expression.In keeping with United Kingdom Coordinating Committee on Cancer Research (UKCCCR) guidelines, the present data indicate the mandatory prerequisite, for investigators involved in human colon cancer research area, of employing mycoplasma-free cell lines in order to avoid the production of non-reproducible or even false data.
支原体污染被认为是连续细胞系培养的一个关键问题。在这项工作中,我们研究了猪鼻支原体污染对人结肠癌细胞系 CD133 表达的影响。
使用 MycoAlert 和支原体琼脂培养法检测 GEO、SW480 和 HT-29 细胞系中的支原体污染。限制性片段长度多态性分析用于确定支原体的种类。所有细胞模型均使用特定的抗生素组合(恩诺沙星、环丙沙星、BM 细胞周期蛋白 1 和 2、支原体去除剂和 MycoZap)进行去污处理。在 GEO、SW480 和 HT-29 细胞系中,通过流式细胞术分析 CD133 阳性细胞的百分比,在消除猪鼻支原体之前和之后。
与用有效的抗生素处理使支原体失活的相同细胞系相比,感染猪鼻支原体的结肠癌细胞系显示出更高比例的 CD133+细胞。当支原体阴性细胞再次被猪鼻支原体感染时,CD133 阳性细胞的比例再次增加。
猪鼻支原体感染对培养的人结肠癌细胞系的质量有重要影响,导致 CD133 表达的肿瘤干细胞比例出现假阳性增加。可能的解释是 (i) 支原体直接参与 CD133 的表达,或 (ii) 对具有组成型 CD133 表达的细胞亚群产生选择压力。根据英国癌症研究协调委员会 (UKCCCR) 的指南,本研究数据表明,从事人结肠癌研究领域的研究人员必须使用无支原体的细胞系,以避免产生不可重复或甚至虚假的数据。