Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis
Abstract Skin is the largest organ of the human body. Skin wound is one of the most common forms of wound. Mesenchymal stromal cells (MSCs) have been used to aid skin wound healing via their paracrine factors. Because the secretome of MSCs can be greatly enriched and amplified by treatment with IFN‐...
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Format: | Article |
Language: | English |
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Wiley
2020-10-01
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Series: | Stem Cells Translational Medicine |
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Online Access: | https://doi.org/10.1002/sctm.19-0241 |
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doaj-95e227d6d28d47b7a07738afce53e162 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mengting Zhu Yunpeng Chu Qianwen Shang Zhiyuan Zheng Yanan Li Lijuan Cao Yongjing Chen Jianchang Cao Oscar K. Lee Ying Wang Gerry Melino Guozhong Lv Changshun Shao Yufang Shi |
spellingShingle |
Mengting Zhu Yunpeng Chu Qianwen Shang Zhiyuan Zheng Yanan Li Lijuan Cao Yongjing Chen Jianchang Cao Oscar K. Lee Ying Wang Gerry Melino Guozhong Lv Changshun Shao Yufang Shi Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis Stem Cells Translational Medicine angiogenesis IFN‐γ mesenchymal stromal cells TNF‐α VEGFC wound healing |
author_facet |
Mengting Zhu Yunpeng Chu Qianwen Shang Zhiyuan Zheng Yanan Li Lijuan Cao Yongjing Chen Jianchang Cao Oscar K. Lee Ying Wang Gerry Melino Guozhong Lv Changshun Shao Yufang Shi |
author_sort |
Mengting Zhu |
title |
Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis |
title_short |
Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis |
title_full |
Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis |
title_fullStr |
Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis |
title_full_unstemmed |
Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesis |
title_sort |
mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through vegfc‐mediated angiogenesis |
publisher |
Wiley |
series |
Stem Cells Translational Medicine |
issn |
2157-6564 2157-6580 |
publishDate |
2020-10-01 |
description |
Abstract Skin is the largest organ of the human body. Skin wound is one of the most common forms of wound. Mesenchymal stromal cells (MSCs) have been used to aid skin wound healing via their paracrine factors. Because the secretome of MSCs can be greatly enriched and amplified by treatment with IFN‐γ and TNF‐α (IT), we here tested whether supernatant derived from MSCs pretreated with IT, designated as S‐MSCs‐IT, possesses improved wound healing effect by using a murine model of cutaneous excision, S‐MSCs‐IT was found to be more potent in promoting angiogenesis, constricting collagen deposition and accelerating wound closure than control supernatant (S‐MSCs) during the healing of skin wound. VEGFC, but not VEGFA, was greatly upregulated by IT and was found to be a key factor in mediating the improved wound healing effect of S‐MSCs‐IT. Our results indicate that the beneficial paracrine effect of MSCs on wound healing can be enhanced by pretreatment with inflammatory cytokines. IT treatment may represent a new strategy for optimizing the therapeutic effect of MSCs on skin injuries. |
topic |
angiogenesis IFN‐γ mesenchymal stromal cells TNF‐α VEGFC wound healing |
url |
https://doi.org/10.1002/sctm.19-0241 |
work_keys_str_mv |
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doaj-95e227d6d28d47b7a07738afce53e1622020-11-25T03:30:31ZengWileyStem Cells Translational Medicine2157-65642157-65802020-10-019101218123210.1002/sctm.19-0241Mesenchymal stromal cells pretreated with pro‐inflammatory cytokines promote skin wound healing through VEGFC‐mediated angiogenesisMengting Zhu0Yunpeng Chu1Qianwen Shang2Zhiyuan Zheng3Yanan Li4Lijuan Cao5Yongjing Chen6Jianchang Cao7Oscar K. Lee8Ying Wang9Gerry Melino10Guozhong Lv11Changshun Shao12Yufang Shi13The First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaCAS Key Laboratory of Tissue Microenvironment and Tumor Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences Shanghai People's Republic of ChinaInstitute for Tissue Engineering and Regenerative Medicine The Chinese University of Hong Kong HongKong People's Republic of ChinaCAS Key Laboratory of Tissue Microenvironment and Tumor Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences Shanghai People's Republic of ChinaDepartment of Experimental Medicine and Biochemical Sciences University of Rome ‘Tor Vergata’ Rome ItalyDepartment of Burn Surgery The 3rd People's Hospital of Wuxi and Wuxi Medical College of Jiangnan University Wuxi People's Republic of ChinaState Key Laboratory of Radiation Medicine and Protection Institutes for Translational Medicine, Soochow University Suzhou People's Republic of ChinaThe First Affiliated Hospital of Soochow University, State Key Laboratory of Radiation Medicine and Protection, Institutes for Translational Medicine Soochow University Medical College Suzhou People's Republic of ChinaAbstract Skin is the largest organ of the human body. Skin wound is one of the most common forms of wound. Mesenchymal stromal cells (MSCs) have been used to aid skin wound healing via their paracrine factors. Because the secretome of MSCs can be greatly enriched and amplified by treatment with IFN‐γ and TNF‐α (IT), we here tested whether supernatant derived from MSCs pretreated with IT, designated as S‐MSCs‐IT, possesses improved wound healing effect by using a murine model of cutaneous excision, S‐MSCs‐IT was found to be more potent in promoting angiogenesis, constricting collagen deposition and accelerating wound closure than control supernatant (S‐MSCs) during the healing of skin wound. VEGFC, but not VEGFA, was greatly upregulated by IT and was found to be a key factor in mediating the improved wound healing effect of S‐MSCs‐IT. Our results indicate that the beneficial paracrine effect of MSCs on wound healing can be enhanced by pretreatment with inflammatory cytokines. IT treatment may represent a new strategy for optimizing the therapeutic effect of MSCs on skin injuries.https://doi.org/10.1002/sctm.19-0241angiogenesisIFN‐γmesenchymal stromal cellsTNF‐αVEGFCwound healing |