Exosomes from human adipose‐derived stem cells promote sciatic nerve regeneration via optimizing Schwann cell function

Human adipose‐derived stem cells (ASCs) have a potential for the treatment of peripheral nerve injury. Recent studies demonstrated that stem cells can mediate therapeutic effect by secreting exosomes. We aimed to investigate the effect of human ASCs derived exosomes (ASC‐Exos) on peripheral nerve re...

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Published inJournal of cellular physiology Vol. 234; no. 12; pp. 23097 - 23110
Main Authors Chen, Jing, Ren, Sen, Duscher, Dominik, Kang, Yu, Liu, Yutian, Wang, Cheng, Yuan, Meng, Guo, Guojun, Xiong, Hewei, Zhan, Peng, Wang, Yang, Machens, Hans‐Günther, Chen, Zhenbing
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.12.2019
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Summary:Human adipose‐derived stem cells (ASCs) have a potential for the treatment of peripheral nerve injury. Recent studies demonstrated that stem cells can mediate therapeutic effect by secreting exosomes. We aimed to investigate the effect of human ASCs derived exosomes (ASC‐Exos) on peripheral nerve regeneration in vitro and in vivo. Our results showed after being internalized by Schwann cells (SCs), ASC‐Exos significantly promoted SC proliferation, migration, myelination, and secretion of neurotrophic factors by upregulating corresponding genes in vitro. We next evaluated the efficacy of ASC‐Exo therapy in a rat sciatic nerve transection model with a 10‐mm gap. Axon regeneration, myelination, and restoration of denervation muscle atrophy in ASC‐Exos treated group was significantly improved compared to vehicle control. This study demonstrates that ASC‐Exos effectively promote peripheral nerve regeneration via optimizing SC function and thereby represent a novel therapeutic strategy for regenerative medicine and nerve tissue engineering. This study demonstrates that ASC‐Exos effectively promote peripheral nerve regeneration via optimizing Schwann cell function and thereby represent a novel therapeutic strategy for regenerative medicine and nerve tissue engineering.
Bibliography:Jing Chen and Sen Ren contributed equally to this study.
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ISSN:0021-9541
1097-4652
1097-4652
DOI:10.1002/jcp.28873