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作 者:曹蕾[1] 杨迷芳[2] 平锋锋[3] 田田[5] 王磊
机构地区:[1]南京医科大学附属无锡第二医院皮肤科,214000 [2]南京医科大学口腔疾病研究所江苏省重点实验室,210029 [3]南京医科大学附属无锡人民医院中心实验室,214000 [4]南京医科大学附属无锡人民医院皮肤科,214000 [5]南京医科大学神经生物学系,210029
出 处:《中华微生物学和免疫学杂志》2016年第1期42-47,共6页Chinese Journal of Microbiology and Immunology
基 金:基金项目:南京医科大学重点项目(2015NJMUZD069);江苏省自然科学基金(BK20130886)
摘 要:目的研究黑素瘤来源的外泌体(exosome)如何与微环境相互作用。 方法分离并鉴定小鼠黑素瘤细胞培养液上清中的外泌体,并与间充质基质细胞(MSC)共培养。利用免疫荧光观察细胞摄入外泌体情况,CCK-8及transwell实验测定MSC增殖与迁移的变化情况,Western blot检测外泌体对MSC的α平滑肌肌动蛋白(α-SMA)表达的影响。 结果发现MSC在摄取外泌体后,增殖和迁移能力显著上升,α-SMA的表达明显上调。且这些变化都可被TGF-β受体的抑制剂阻断。 结论外泌体可能通过TGF-β诱导MSC构建微环境,促进黑素瘤的生长与转移。ObjectiveTo investigate the interactions between melanoma-derived exosomes and the microenvironment. MethodsThe exosomes were isolated from the culture medium of mouse melanoma cells and then co-cultured with mesenchymal stromal cells (MSC) after identification. Immunofluorescence assay was performed to observe the exosomes engulfed by MSC. CCK-8 and transwell assays were used to evaluate the proliferation and migration of MSC. Effects of the exosomes on the expression of α-smooth muscle actin (α-SMA) in MSC were analyzed by Western blot. ResultsCo-culture of MSC with melanoma cell-derived exosomes enhanced the proliferation and migration of MSC as well as the expression of α-SMA. All of the changes mediated by the exosomes could be blocked by using the inhibitor of TGF-β receptor. ConclusionMelanoma cell-derived exosomes enhanced the proliferation and migration of MSC as well as the expression of α-SMA through TGF-β signaling pathway, which provided an advantageous microenvironment for melanoma progression.
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