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Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy

OBJECTIVE: To evaluate the therapeutic potential of stem cells from human exfoliated deciduous teeth (SHED) for diabetic peripheral neuropathy. METHODS: The biological characteristics of SHED were identified by flow cytometric study and evaluation of differentiation potential. Using high-fat feeding...

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Autores principales: Xie, Jing, Rao, Nanquan, Zhai, Yue, Li, Jingzhi, Zhao, Yuming, Ge, Lihong, Wang, Yuanyuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525430/
https://www.ncbi.nlm.nih.gov/pubmed/31131042
http://dx.doi.org/10.1186/s13098-019-0433-y
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author Xie, Jing
Rao, Nanquan
Zhai, Yue
Li, Jingzhi
Zhao, Yuming
Ge, Lihong
Wang, Yuanyuan
author_facet Xie, Jing
Rao, Nanquan
Zhai, Yue
Li, Jingzhi
Zhao, Yuming
Ge, Lihong
Wang, Yuanyuan
author_sort Xie, Jing
collection PubMed
description OBJECTIVE: To evaluate the therapeutic potential of stem cells from human exfoliated deciduous teeth (SHED) for diabetic peripheral neuropathy. METHODS: The biological characteristics of SHED were identified by flow cytometric study and evaluation of differentiation potential. Using high-fat feeding, diabetes was induced in GK rats, and SHED were transplanted into the caudal veins of these rats. Immunohistochemical analysis was used to compare the capillary to muscle fiber ratio and intra-epidermal nerve fiber density between SHED- and saline-treated diabetic rats. Further, the expressions of angiogenesis-related and neurotrophic factors were quantified by real-time PCR and western blot. RESULTS: SHED had a capacity of multiple differentiation and shared typical characteristics of mesenchymal stem cells. SHED transplantation relieved diabetic neuropathic pain, enabled functional recovery of the peripheral nerves, and increased the capillary to muscle fiber ratio and intra-epidermal nerve fiber density compared to the saline group and normal controls. Real-time PCR results showed that the expressions of CD31, vWF, bFGF, NGF, and NT-3 in the skeletal muscles were higher in the SHED group than in the saline groups. Western blot results indicated that the levels of the CD31 and NGF proteins were higher in the SHED transplantation group than the saline group. CONCLUSION: SHED transplantation ameliorated diabetic peripheral neuropathy in diabetic GK rats. Thus, systemic application of SHED could be a novel strategy for the treatment of diabetic peripheral neuropathy.
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spelling pubmed-65254302019-05-24 Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy Xie, Jing Rao, Nanquan Zhai, Yue Li, Jingzhi Zhao, Yuming Ge, Lihong Wang, Yuanyuan Diabetol Metab Syndr Research OBJECTIVE: To evaluate the therapeutic potential of stem cells from human exfoliated deciduous teeth (SHED) for diabetic peripheral neuropathy. METHODS: The biological characteristics of SHED were identified by flow cytometric study and evaluation of differentiation potential. Using high-fat feeding, diabetes was induced in GK rats, and SHED were transplanted into the caudal veins of these rats. Immunohistochemical analysis was used to compare the capillary to muscle fiber ratio and intra-epidermal nerve fiber density between SHED- and saline-treated diabetic rats. Further, the expressions of angiogenesis-related and neurotrophic factors were quantified by real-time PCR and western blot. RESULTS: SHED had a capacity of multiple differentiation and shared typical characteristics of mesenchymal stem cells. SHED transplantation relieved diabetic neuropathic pain, enabled functional recovery of the peripheral nerves, and increased the capillary to muscle fiber ratio and intra-epidermal nerve fiber density compared to the saline group and normal controls. Real-time PCR results showed that the expressions of CD31, vWF, bFGF, NGF, and NT-3 in the skeletal muscles were higher in the SHED group than in the saline groups. Western blot results indicated that the levels of the CD31 and NGF proteins were higher in the SHED transplantation group than the saline group. CONCLUSION: SHED transplantation ameliorated diabetic peripheral neuropathy in diabetic GK rats. Thus, systemic application of SHED could be a novel strategy for the treatment of diabetic peripheral neuropathy. BioMed Central 2019-05-17 /pmc/articles/PMC6525430/ /pubmed/31131042 http://dx.doi.org/10.1186/s13098-019-0433-y Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Xie, Jing
Rao, Nanquan
Zhai, Yue
Li, Jingzhi
Zhao, Yuming
Ge, Lihong
Wang, Yuanyuan
Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title_full Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title_fullStr Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title_full_unstemmed Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title_short Therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
title_sort therapeutic effects of stem cells from human exfoliated deciduous teeth on diabetic peripheral neuropathy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6525430/
https://www.ncbi.nlm.nih.gov/pubmed/31131042
http://dx.doi.org/10.1186/s13098-019-0433-y
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