Cargando…
Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect
Poor viability of engrafted bone marrow mesenchymal stem cells (BMSCs) often hinders their application for wound healing, and the strategy of how to take full advantage of their angiogenic capacity within wounds still remains unclear. Negative pressure wound therapy (NPWT) has been demonstrated to b...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294348/ https://www.ncbi.nlm.nih.gov/pubmed/28243602 http://dx.doi.org/10.1155/2017/7920265 |
_version_ | 1782505221788794880 |
---|---|
author | Shou, Kangquan Niu, Yahui Zheng, Xun Ma, Zhanjun Jian, Chao Qi, Baiwen Hu, Xiang Yu, Aixi |
author_facet | Shou, Kangquan Niu, Yahui Zheng, Xun Ma, Zhanjun Jian, Chao Qi, Baiwen Hu, Xiang Yu, Aixi |
author_sort | Shou, Kangquan |
collection | PubMed |
description | Poor viability of engrafted bone marrow mesenchymal stem cells (BMSCs) often hinders their application for wound healing, and the strategy of how to take full advantage of their angiogenic capacity within wounds still remains unclear. Negative pressure wound therapy (NPWT) has been demonstrated to be effective for enhancing wound healing, especially for the promotion of angiogenesis within wounds. Here we utilized combinatory strategy using the transplantation of BMSCs and NPWT to investigate whether this combinatory therapy could accelerate angiogenesis in wounds. In vitro, after 9-day culture, BMSCs proliferation significantly increased in NPWT group. Furthermore, NPWT induced their differentiation into the angiogenic related cells, which are indispensable for wound angiogenesis. In vivo, rat full-thickness cutaneous wounds treated with BMSCs combined with NPWT exhibited better viability of the cells and enhanced angiogenesis and maturation of functional blood vessels than did local BMSC injection or NPWT alone. Expression of angiogenesis markers (NG2, VEGF, CD31, and α-SMA) was upregulated in wounds treated with combined BMSCs with NPWT. Our data suggest that NPWT may act as an inductive role to enhance BMSCs angiogenic capacity and this combinatorial therapy may serve as a simple but efficient clinical solution for complex wounds with large defects. |
format | Online Article Text |
id | pubmed-5294348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-52943482017-02-27 Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect Shou, Kangquan Niu, Yahui Zheng, Xun Ma, Zhanjun Jian, Chao Qi, Baiwen Hu, Xiang Yu, Aixi Biomed Res Int Research Article Poor viability of engrafted bone marrow mesenchymal stem cells (BMSCs) often hinders their application for wound healing, and the strategy of how to take full advantage of their angiogenic capacity within wounds still remains unclear. Negative pressure wound therapy (NPWT) has been demonstrated to be effective for enhancing wound healing, especially for the promotion of angiogenesis within wounds. Here we utilized combinatory strategy using the transplantation of BMSCs and NPWT to investigate whether this combinatory therapy could accelerate angiogenesis in wounds. In vitro, after 9-day culture, BMSCs proliferation significantly increased in NPWT group. Furthermore, NPWT induced their differentiation into the angiogenic related cells, which are indispensable for wound angiogenesis. In vivo, rat full-thickness cutaneous wounds treated with BMSCs combined with NPWT exhibited better viability of the cells and enhanced angiogenesis and maturation of functional blood vessels than did local BMSC injection or NPWT alone. Expression of angiogenesis markers (NG2, VEGF, CD31, and α-SMA) was upregulated in wounds treated with combined BMSCs with NPWT. Our data suggest that NPWT may act as an inductive role to enhance BMSCs angiogenic capacity and this combinatorial therapy may serve as a simple but efficient clinical solution for complex wounds with large defects. Hindawi Publishing Corporation 2017 2017-01-24 /pmc/articles/PMC5294348/ /pubmed/28243602 http://dx.doi.org/10.1155/2017/7920265 Text en Copyright © 2017 Kangquan Shou et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Shou, Kangquan Niu, Yahui Zheng, Xun Ma, Zhanjun Jian, Chao Qi, Baiwen Hu, Xiang Yu, Aixi Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title | Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title_full | Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title_fullStr | Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title_full_unstemmed | Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title_short | Enhancement of Bone-Marrow-Derived Mesenchymal Stem Cell Angiogenic Capacity by NPWT for a Combinatorial Therapy to Promote Wound Healing with Large Defect |
title_sort | enhancement of bone-marrow-derived mesenchymal stem cell angiogenic capacity by npwt for a combinatorial therapy to promote wound healing with large defect |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294348/ https://www.ncbi.nlm.nih.gov/pubmed/28243602 http://dx.doi.org/10.1155/2017/7920265 |
work_keys_str_mv | AT shoukangquan enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT niuyahui enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT zhengxun enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT mazhanjun enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT jianchao enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT qibaiwen enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT huxiang enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect AT yuaixi enhancementofbonemarrowderivedmesenchymalstemcellangiogeniccapacitybynpwtforacombinatorialtherapytopromotewoundhealingwithlargedefect |