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Nanosecond pulsed electric fields prime mesenchymal stem cells to peptide ghrelin and enhance chondrogenesis and osteochondral defect repair in vivo.
Li, Kejia; Fan, Litong; Lin, Jianjing; Heng, Boon Chin; Deng, Zhantao; Zheng, Qiujian; Zhang, Jue; Jiang, Yangzi; Ge, Zigang.
Afiliação
  • Li K; Department of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
  • Fan L; Department of Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
  • Lin J; Arthritis Clinical and Research Center, Peking University People's Hospital, Beijing, 100044, China.
  • Heng BC; Arthritis Institute, Peking University, Beijing, 100871, China.
  • Deng Z; Peking University School of Stomatology, Beijing, 100081, China.
  • Zheng Q; Department of Orthopedics, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, China.
  • Zhang J; Department of Orthopedics, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, China.
  • Jiang Y; Institute of Biomechanics and Biomedical Engineering, College of Engineering, Peking University, Beijing, 100871, China.
  • Ge Z; Institute for Tissue Engineering and Regenerative Medicine, School of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong, 999077, China. yangzjiang21@cuhk.edu.hk.
Sci China Life Sci ; 65(5): 927-939, 2022 05.
Article em En | MEDLINE | ID: mdl-34586575
Mesenchymal stem cells (MSCs) are important cell sources in cartilage tissue development and homeostasis, and multiple strategies have been developed to improve MSCs chondrogenic differentiation with an aim of promoting cartilage regeneration. Here we report the effects of combining nanosecond pulsed electric fields (nsPEFs) followed by treatment with ghrelin (a hormone that stimulates release of growth hormone) to regulate chondrogenesis of MSCs. nsPEFs and ghrelin were observed to separately enhance the chondrogenesis of MSCs, and the effects were significantly enhanced when the bioelectric stimulation and hormone were combined, which in turn improved osteochondral tissue repair of these cells within Sprague Dawley rats. We further found that nsPEFs can prime MSCs to be more receptive to subsequent stimuli of differentiation by upregulated Oct4/Nanog and activated JNK signaling pathway. Ghrelin initiated chondrogenic differentiation by activation of ERK1/2 signaling pathway, and RNA-seq results indicated 243 genes were regulated, and JAK-STAT signaling pathway was involved. Interestingly, the sequential order of applying these two stimuli is critical, with nsPEFs pretreatment followed by ghrelin enhanced chondrogenesis of MSCs in vitro and subsequent cartilage regeneration in vivo, but not vice versa. This synergistic prochondrogenic effects provide us new insights and strategies for future cell-based therapies.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condrogênese / Células-Tronco Mesenquimais Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Condrogênese / Células-Tronco Mesenquimais Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article