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Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect

Stem cells derived extracellular vesicles (EVs) conceive cues essential for tissue repair. Mammalian cartilaginous extracellular matrix (cECM) may not be optimally inductive for tracheal regeneration because of the granulomatous, instead of regenerative, responses in injured adult mammalian tracheas...

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Autores principales: Zeng, Tian, Yuan, Pingping, Liang, Lirong, Zhang, Xinchi, Zhang, Hui, Wu, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805569/
https://www.ncbi.nlm.nih.gov/pubmed/34841733
http://dx.doi.org/10.1002/advs.202102735
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author Zeng, Tian
Yuan, Pingping
Liang, Lirong
Zhang, Xinchi
Zhang, Hui
Wu, Wei
author_facet Zeng, Tian
Yuan, Pingping
Liang, Lirong
Zhang, Xinchi
Zhang, Hui
Wu, Wei
author_sort Zeng, Tian
collection PubMed
description Stem cells derived extracellular vesicles (EVs) conceive cues essential for tissue repair. Mammalian cartilaginous extracellular matrix (cECM) may not be optimally inductive for tracheal regeneration because of the granulomatous, instead of regenerative, responses in injured adult mammalian tracheas. Given the high regenerative capacity of gingiva, it is hypothesized human gingival mesenchymal stem cells derived EVs (gEVs) can induce mammalian tracheal epithelia regeneration. Coculturing chondrocytes with GMSCs produce abundant “matrix bound gEVs (gMVs)” in forming cartilaginous ECM, which are further preserved in acellular cECM (cACM) following mild, short‐period decellularization. The results show that gMVs‐cACM could be well anchored on polyglycerol sebacate microporous patch thus enforce the surgical suturability and mechanical strength. In rabbit tracheal defect, the gMVs‐cACM patch induces rapid regeneration of vascularized ciliated columnar epithelium, which supports long‐term survival of animals. gMVs‐cACM treated groups exhibit proliferation of tracheal progenitors‐basal epithelial cells, as well as, activation of JAK2/STAT1 pathway in reparative cells. This study departs from conventional focuses on tissue derived ECM and introduces a new approach for tracheal tissue regeneration.
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spelling pubmed-88055692022-02-04 Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect Zeng, Tian Yuan, Pingping Liang, Lirong Zhang, Xinchi Zhang, Hui Wu, Wei Adv Sci (Weinh) Research Articles Stem cells derived extracellular vesicles (EVs) conceive cues essential for tissue repair. Mammalian cartilaginous extracellular matrix (cECM) may not be optimally inductive for tracheal regeneration because of the granulomatous, instead of regenerative, responses in injured adult mammalian tracheas. Given the high regenerative capacity of gingiva, it is hypothesized human gingival mesenchymal stem cells derived EVs (gEVs) can induce mammalian tracheal epithelia regeneration. Coculturing chondrocytes with GMSCs produce abundant “matrix bound gEVs (gMVs)” in forming cartilaginous ECM, which are further preserved in acellular cECM (cACM) following mild, short‐period decellularization. The results show that gMVs‐cACM could be well anchored on polyglycerol sebacate microporous patch thus enforce the surgical suturability and mechanical strength. In rabbit tracheal defect, the gMVs‐cACM patch induces rapid regeneration of vascularized ciliated columnar epithelium, which supports long‐term survival of animals. gMVs‐cACM treated groups exhibit proliferation of tracheal progenitors‐basal epithelial cells, as well as, activation of JAK2/STAT1 pathway in reparative cells. This study departs from conventional focuses on tissue derived ECM and introduces a new approach for tracheal tissue regeneration. John Wiley and Sons Inc. 2021-11-28 /pmc/articles/PMC8805569/ /pubmed/34841733 http://dx.doi.org/10.1002/advs.202102735 Text en © 2021 The Authors. Advanced Science published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zeng, Tian
Yuan, Pingping
Liang, Lirong
Zhang, Xinchi
Zhang, Hui
Wu, Wei
Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title_full Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title_fullStr Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title_full_unstemmed Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title_short Cartilaginous Extracellular Matrix Enriched with Human Gingival Mesenchymal Stem Cells Derived “Matrix Bound Extracellular Vesicles” Enabled Functional Reconstruction of Tracheal Defect
title_sort cartilaginous extracellular matrix enriched with human gingival mesenchymal stem cells derived “matrix bound extracellular vesicles” enabled functional reconstruction of tracheal defect
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8805569/
https://www.ncbi.nlm.nih.gov/pubmed/34841733
http://dx.doi.org/10.1002/advs.202102735
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