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Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination

Wound repair is accomplished by the interaction between the cells involved in the repair and the extracellular matrix (ECM). Collagen is the main component of ECM, which is involved in transduction of signal, transportation of growth factors and cytokines. Fibronectin (FN) is also an important ECM,...

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Autores principales: Dong, Yunqing, Zhu, Weidong, Lei, Xiaoxuan, Luo, Xin, Xiang, Qi, Zhu, Xuanru, Pan, Qiao, Jin, Panshi, Cheng, Biao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160431/
https://www.ncbi.nlm.nih.gov/pubmed/35662842
http://dx.doi.org/10.3389/fbioe.2022.908585
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author Dong, Yunqing
Zhu, Weidong
Lei, Xiaoxuan
Luo, Xin
Xiang, Qi
Zhu, Xuanru
Pan, Qiao
Jin, Panshi
Cheng, Biao
author_facet Dong, Yunqing
Zhu, Weidong
Lei, Xiaoxuan
Luo, Xin
Xiang, Qi
Zhu, Xuanru
Pan, Qiao
Jin, Panshi
Cheng, Biao
author_sort Dong, Yunqing
collection PubMed
description Wound repair is accomplished by the interaction between the cells involved in the repair and the extracellular matrix (ECM). Collagen is the main component of ECM, which is involved in transduction of signal, transportation of growth factors and cytokines. Fibronectin (FN) is also an important ECM, which participates in the initiation of fibroblast cell (FC) and promotes adhesion, migration, proliferation and differentiation of target cells. Compared with natural protein, the recombinant protein prepared by artificial method has the advantages of poor immunogenicity, wide range of sources, low cost and high activity. In this study, we used recombinant human-like collagen (RHC) and recombinant human-like fibronectin (rhFN) to treat acute wounds in C57BL/6 mice individually or in combination, and explored their effects on wound healing. Our study confirmed that these two recombinant proteins could effectively promote the proliferation, migration and adhesion of FCs. Meanwhile, it could positively regulate the healing speed and quality of acute wounds, re-epithelialization, collagen deposition, inflammation and angiogenesis. Moreover, we proved that the combination of the two was better than the treatment alone. Consequently, it has a good prospect as a new tissue material in the field of skin repair.
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spelling pubmed-91604312022-06-03 Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination Dong, Yunqing Zhu, Weidong Lei, Xiaoxuan Luo, Xin Xiang, Qi Zhu, Xuanru Pan, Qiao Jin, Panshi Cheng, Biao Front Bioeng Biotechnol Bioengineering and Biotechnology Wound repair is accomplished by the interaction between the cells involved in the repair and the extracellular matrix (ECM). Collagen is the main component of ECM, which is involved in transduction of signal, transportation of growth factors and cytokines. Fibronectin (FN) is also an important ECM, which participates in the initiation of fibroblast cell (FC) and promotes adhesion, migration, proliferation and differentiation of target cells. Compared with natural protein, the recombinant protein prepared by artificial method has the advantages of poor immunogenicity, wide range of sources, low cost and high activity. In this study, we used recombinant human-like collagen (RHC) and recombinant human-like fibronectin (rhFN) to treat acute wounds in C57BL/6 mice individually or in combination, and explored their effects on wound healing. Our study confirmed that these two recombinant proteins could effectively promote the proliferation, migration and adhesion of FCs. Meanwhile, it could positively regulate the healing speed and quality of acute wounds, re-epithelialization, collagen deposition, inflammation and angiogenesis. Moreover, we proved that the combination of the two was better than the treatment alone. Consequently, it has a good prospect as a new tissue material in the field of skin repair. Frontiers Media S.A. 2022-05-19 /pmc/articles/PMC9160431/ /pubmed/35662842 http://dx.doi.org/10.3389/fbioe.2022.908585 Text en Copyright © 2022 Dong, Zhu, Lei, Luo, Xiang, Zhu, Pan, Jin and Cheng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Bioengineering and Biotechnology
Dong, Yunqing
Zhu, Weidong
Lei, Xiaoxuan
Luo, Xin
Xiang, Qi
Zhu, Xuanru
Pan, Qiao
Jin, Panshi
Cheng, Biao
Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title_full Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title_fullStr Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title_full_unstemmed Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title_short Treatment of Acute Wounds With Recombinant Human-Like Collagen and Recombinant Human-Like Fibronectin in C57BL/6 Mice Individually or in Combination
title_sort treatment of acute wounds with recombinant human-like collagen and recombinant human-like fibronectin in c57bl/6 mice individually or in combination
topic Bioengineering and Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9160431/
https://www.ncbi.nlm.nih.gov/pubmed/35662842
http://dx.doi.org/10.3389/fbioe.2022.908585
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