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GelMA loaded with exosomes from human minor salivary gland organoids enhances wound healing by inducing macrophage polarization.
Qian, Jiaying; Lu, Enhang; Xiang, Haibo; Ding, Pengbing; Wang, Zheng; Lin, Zhiyu; Pan, Bolin; Zhang, Chen; Zhao, Zhenmin.
Afiliação
  • Qian J; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Lu E; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China. 2011110439@bjmu.edu.cn.
  • Xiang H; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Ding P; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Wang Z; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Lin Z; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Pan B; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China.
  • Zhang C; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China. zhangchenpumc@qq.com.
  • Zhao Z; Department of Plastic Surgery, Peking University Third Hospital, Beijing, 100191, China. zzmbysy@sina.com.
J Nanobiotechnology ; 22(1): 550, 2024 Sep 06.
Article em En | MEDLINE | ID: mdl-39243057
ABSTRACT
Non-healing skin wounds pose significant clinical challenges, with biologic products like exosomes showing promise for wound healing. Saliva and saliva-derived exosomes, known to accelerate wound repair, yet their extraction is difficult due to the complex environment of oral cavity. In this study, as a viable alternative, we established human minor salivary gland organoids (hMSG-ORG) to produce exosomes (MsOrg-Exo). In vitro, MsOrg-Exo significantly enhanced cell proliferation, migration, and angiogenesis. When incorporated into a GelMA-based controlled-release system, MsOrg-Exo demonstrated controlled release, effectively improving wound closure, collagen synthesis, angiogenesis, and cellular proliferation in a murine skin wound model. Further molecular analyses revealed that MsOrg-Exo promotes proliferation, angiogenesis and the secretion of growth factors in wound sites. Proteomic profiling showed that MsOrg-Exo's protein composition is similar to human saliva and enriched in proteins essential for wound repair, immune modulation, and coagulation. Additionally, MsOrg-Exo was found to modulate macrophage polarization, inducing a shift towards M1 and M2 phenotypes in vitro within 48 h and predominantly towards the M2 phenotype in vivo after 15 days. In conclusion, our study successfully extracted MsOrg-Exo from hMSG-ORGs, confirmed the effectiveness of the controlled-release system combining MsOrg-Exo with GelMA in promoting skin wound healing, and explored the potential role of macrophages in this action.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cicatrização / Organoides / Exossomos / Macrófagos Limite: Animals / Humans Idioma: En Revista: J Nanobiotechnology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cicatrização / Organoides / Exossomos / Macrófagos Limite: Animals / Humans Idioma: En Revista: J Nanobiotechnology Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido