Department of Otorhinolaryngology, Yonsei University Wonju College of Medicine, 20 Ilsan- ro, Wonju, Gangwon-do, 26426, South Korea.
Research Institute of Hearing Enhancement, Wonju, Gangwon-do, 26426, South Korea.
J Nanobiotechnology. 2021 May 20;19(1):148. doi: 10.1186/s12951-021-00890-9.
The application of extracellular vesicles (EVs) derived from mesenchymal stem cells (MSCs) requires customized materials to target disease or cell damage. We hypothesized that EVs exert different inflammatory effects on one recipient cell, although stem cells of different origins in humans have similar payloads.
Here, the payload of EVs released by crosstalk between MSCs and human middle ear epithelial cells (HMEECs) extracted from adipose tissue, bone marrow and tonsils significantly increased the level of anti-inflammatory factors. EVs derived from the co-culture medium decreased TNF-α, COX-2, IL-1β, and IL-6 levels to approximately zero within 3 h in HMEECs. Expression of miR-638 and amyloid-β A4 precursor protein-binding family A member 2 was analyzed using microarrays and gene ontology analysis, respectively.
In conclusion, stem cells of different origins have different payloads through crosstalk with recipient-specific cells. Inducing specific factors in EVs by co-culture with MSCs could be valuable in regenerative medicine.
间充质干细胞(MSCs)衍生的细胞外囊泡(EVs)的应用需要定制材料来靶向疾病或细胞损伤。我们假设,尽管来自不同来源的干细胞在人类中有相似的有效负载,但 EVs 对一个受体细胞发挥不同的炎症作用。
在这里,从脂肪组织、骨髓和扁桃体中提取的 MSC 与人中耳上皮细胞(HMEEC)之间的细胞间通讯释放的 EV 的有效负载显著增加了抗炎因子的水平。源自共培养培养基的 EV 在 3 小时内将 HMEEC 中的 TNF-α、COX-2、IL-1β 和 IL-6 水平降低至接近零。使用微阵列分析 miR-638 的表达,分别使用基因本体分析分析淀粉样蛋白-β A4 前体蛋白结合家族 A 成员 2 的表达。
总之,通过与受体特异性细胞的细胞间通讯,不同来源的干细胞具有不同的有效负载。通过与 MSC 共培养诱导 EV 中的特定因子可能在再生医学中具有价值。