Comparison of exosomes derived from induced pluripotent stem cells and mesenchymal stem cells as therapeutic nanoparticles for treatment of corneal epithelial defects.
Comparison of exosomes derived from induced pluripotent stem cells and mesenchymal stem cells as therapeutic nanoparticles for treatment of corneal epithelial defects.
复制标题
诱导多能干细胞和间充质干细胞来源的外泌体作为治疗角膜上皮缺陷的治疗性纳米颗粒的比较
DOI:
10.18632/aging.103904
复制
发表时间:
2020-10-13
期刊:
影响因子:
--
通讯作者:
Zhang H
中科院分区:
文献类型:
--
作者:
Wang S;Hou Y;Li X;Song Z;Sun B;Li X;Zhang H
Induced pluripotent stem cells and mesenchymal stem cells are pluripotent stem cells that represent promising therapies for treating various tissue injuries and wound healing. Exosomes are nanosized extracellular vesicles that have been identified as important mediators of therapeutic functions, which are performed via cell communication. In this study, we compared the efficacy of induced pluripotent stem cells-derived exosomes (iPSCs-Exos) and mesenchymal stem cells-derived exosomes (MSCs-Exos) in treating corneal epithelial defects. The characteristics of the two types of exosomes were not significantly different. Compared to MSCs-Exos, iPSCs-Exos had a better in vitro effect on the proliferation, migration, cell cycle promotion and apoptosis inhibition of human corneal epithelial cells. iPSCs/MSCs-Exos promoted cell regeneration by upregulating cyclin A and CDK2 to drive HCECs to enter the S phase from the G0/G1 phase. In vivo results from a corneal epithelial defect model showed that both iPSCs-Exos and MSCs-Exos accelerated corneal epithelium defect healing while the effects of iPSCs-Exos were much stronger than those of MSCs-Exos. This study demonstrated that iPSCs-Exos had a better therapeutic effect on corneal epithelial defect healing. Thus, a novel potential nanotherapeutic strategy for treating corneal epithelial defects and even more ocular surface disease could be undertaken by using iPSCs-Exos dissolved in eye drops.
登录
查看更多内容
影响因子:
16
作者:
Lötvall J;Hill AF;Hochberg F;Buzás EI;Di Vizio D;Gardiner C;Gho YS;Kurochkin IV;Mathivanan S;Quesenberry P;Sahoo S;Tahara H;Wauben MH;Witwer KW;Théry C
通讯作者:
Théry C
DOI:
10.1007/10_2012_156
发表时间:
2013-01-01
期刊:
MESENCHYMAL STEM CELLS: BASICS AND CLINICAL APPLICATION II
影响因子:
--
作者:
Eberle, Irina;Moslem, Mohsen;Cantz, Tobias
通讯作者:
Cantz, Tobias
影响因子:
17.8
作者:
Ljubimov AV;Saghizadeh M
通讯作者:
Saghizadeh M
影响因子:
--
作者:
Mort RL;Ramaesh T;Kleinjan DA;Morley SD;West JD
通讯作者:
West JD
影响因子:
4.6
作者:
Hu L;Li Y;Zhang X;Wang Y;Cui L;Wei Q;Ma H;Yan L;Du B
通讯作者:
Du B