Therapeutic effects of peripherally administrated neural crest stem cells on pain and spinal cord changes after sciatic nerve transection

dc.contributor.authorZhang, Yangen
dc.contributor.authorXu, Xiangen
dc.contributor.authorTong, Yuxinen
dc.contributor.authorZhou, Xijieen
dc.contributor.authorDu, Jianen
dc.contributor.authorChoi, In Y.en
dc.contributor.authorYue, Shouweien
dc.contributor.authorLee, Gabsangen
dc.contributor.authorJohnson, Blake N.en
dc.contributor.authorJia, Xiaofengen
dc.contributor.departmentIndustrial and Systems Engineeringen
dc.contributor.departmentSchool of Neuroscienceen
dc.date.accessioned2021-03-22T11:57:55Zen
dc.date.available2021-03-22T11:57:55Zen
dc.date.issued2021-03-15en
dc.date.updated2021-03-21T04:25:04Zen
dc.description.abstractBackground Severe peripheral nerve injury significantly affects patients’ quality of life and induces neuropathic pain. Neural crest stem cells (NCSCs) exhibit several attractive characteristics for cell-based therapies following peripheral nerve injury. Here, we investigate the therapeutic effect of NCSC therapy and associated changes in the spinal cord in a sciatic nerve transection (SNT) model. Methods Complex sciatic nerve gap injuries in rats were repaired with cell-free and cell-laden nerve scaffolds for 12 weeks (scaffold and NCSC groups, respectively). Catwalk gait analysis was used to assess the motor function recovery. The mechanical withdrawal threshold and thermal withdrawal latency were used to assess the development of neuropathic pain. Activation of glial cells was examined by immunofluorescence analyses. Spinal levels of extracellular signal-regulated kinase (ERK), NF-κB P65, brain-derived neurotrophic factor (BDNF), growth-associated protein (GAP)-43, calcitonin gene-related peptide (CGRP), and inflammation factors were calculated by western blot analysis. Results Catwalk gait analysis showed that animals in the NCSC group exhibited a higher stand index and Max intensity At (%) relative to those that received the cell-free scaffold (scaffold group) (p < 0.05). The mechanical and thermal allodynia in the medial-plantar surface of the ipsilateral hind paw were significantly relieved in the NCSC group. Sunitinib (SNT)-induced upregulation of glial fibrillary acidic protein (GFAP) (astrocyte) and ionized calcium-binding adaptor molecule 1 (Iba-1) (microglia) in the ipsilateral L4–5 dorsal and ventral horn relative to the contralateral side. Immunofluorescence analyses revealed decreased astrocyte and microglia activation. Activation of ERK and NF-κB signals and expression of transient receptor potential vanilloid 1 (TRPV1) expression were downregulated. Conclusion NCSC-laden nerve scaffolds mitigated SNT-induced neuropathic pain and improved motor function recovery after sciatic nerve repair. NCSCs also protected the spinal cord from SNT-induced glial activation and central sensitization.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationStem Cell Research & Therapy. 2021 Mar 15;12(1):180en
dc.identifier.doihttps://doi.org/10.1186/s13287-021-02200-4en
dc.identifier.urihttp://hdl.handle.net/10919/102754en
dc.language.isoenen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.holderThe Author(s)en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.titleTherapeutic effects of peripherally administrated neural crest stem cells on pain and spinal cord changes after sciatic nerve transectionen
dc.title.serialStem Cell Research & Therapyen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten
dc.type.dcmitypeStillImageen

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