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Effect of exosomes from adipose-derived stem cells on the apoptosis of Schwann cells in peripheral nerve injury.
Liu, Cai-Yue; Yin, Gang; Sun, Yi-Dan; Lin, Yao-Fa; Xie, Zheng; English, Arthur W; Li, Qing-Feng; Lin, Hao-Dong.
Afiliação
  • Liu CY; Department of Orthopedic Surgery, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Yin G; Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Sun YD; Department of Plastic Surgery, Changzheng Hospital, The Navy Military Medical University, Shanghai, China.
  • Lin YF; Department of Orthopedic Surgery, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Xie Z; Department of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • English AW; Department of Orthopedic Surgery, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
  • Li QF; Department of Orthopedic Surgery, Changzheng Hospital, The Navy Military Medical University, Shanghai, China.
  • Lin HD; Department of Orthopedic Surgery, Shanghai General Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China.
CNS Neurosci Ther ; 26(2): 189-196, 2020 02.
Article em En | MEDLINE | ID: mdl-31278850
AIMS: Recovery after peripheral nerve injury (PNI) is often difficult, and there is no optimal treatment. Schwann cells (SCs) are important for peripheral nerve regeneration, so SC-targeting treatments have gained importance. Adipose-derived stem cells (ADSCs) and their exosomes can promote peripheral nerve repair, but their interactions with SCs are unclear. METHODS: Purified SCs from sciatic nerve injury sites were harvested, and apoptosis and proliferation of SCs at post-PNI 24 hours were analyzed. The effects of coculture with ADSCs and different concentrations of ADSC-derived exosomes (ADSC-Exo) were studied through in vitro experiments by flow cytometry, CCK8 assay, immunofluorescence staining, and histological analysis. The expression of the apoptosis-related genes Bcl-2 and Bax was also analyzed by qRT-PCR. RESULTS: ADSC-Exo reduced the apoptosis of SCs after PNI by upregulating the anti-apoptotic Bcl-2 mRNA expression and downregulating the pro-apoptotic Bax mRNA expression. Further, it also improved the proliferation rate of SCs. This effect was confirmed by the morphological and histological findings in PNI model rats. CONCLUSION: Our results present a novel exosome-mediated mechanism for ADSC-SC cross talk that reduces the apoptosis and promotes the proliferation of SCs and may have therapeutic potential in the future.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células de Schwann / Células-Tronco / Tecido Adiposo / Apoptose / Exossomos / Traumatismos dos Nervos Periféricos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: CNS Neurosci Ther Assunto da revista: NEUROLOGIA / TERAPEUTICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células de Schwann / Células-Tronco / Tecido Adiposo / Apoptose / Exossomos / Traumatismos dos Nervos Periféricos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: CNS Neurosci Ther Assunto da revista: NEUROLOGIA / TERAPEUTICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China