3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization

Scar contraction frequently happens in patients with deep burn injuries. Hitherto, porcine dermal extracellular matrix (dECM) has supplied microenvironments that assist in wound healing but fail to inhibit scar contraction. To overcome this drawback, we integrate dECM into three-dimensional (3D)-pri...

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Autores principales: Lei Chen, Zhiyong Li, Yongtai Zheng, Fei Zhou, Jingling Zhao, Qiyi Zhai, Zhaoqiang Zhang, Tianrun Liu, Yongming Chen, Shaohai Qi
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Publicado: KeAi Communications Co., Ltd. 2022
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spelling oai:doaj.org-article:b6fae460aa79463db07b5c6e92804fbf2021-11-28T04:35:32Z3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization2452-199X10.1016/j.bioactmat.2021.09.008https://doaj.org/article/b6fae460aa79463db07b5c6e92804fbf2022-04-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2452199X21004187https://doaj.org/toc/2452-199XScar contraction frequently happens in patients with deep burn injuries. Hitherto, porcine dermal extracellular matrix (dECM) has supplied microenvironments that assist in wound healing but fail to inhibit scar contraction. To overcome this drawback, we integrate dECM into three-dimensional (3D)-printed dermal analogues (PDA) to prevent scar contraction. We have developed thermally gelled, non-rheologically modified dECM powder (dECMp) inks and successfully transformed them into PDA that was endowed with a micron-scale spatial structure. The optimal crosslinked PDA exhibited desired structure, good mechanical properties as well as excellent biocompatibility. Moreover, in vivo experiments demonstrated that PDA could significantly reduced scar contraction and improved cosmetic upshots of split thickness skin grafts (STSG) than the commercially available dermal templates and STSG along. The PDA has also induced an early, intense neovascularization, and evoked a type-2-like immune response. PDA's superior beneficial effects may attribute to their desired porous structure, the well-balanced physicochemical properties, and the preserved dermis-specific ECM cues, which collectively modulated the expression of genes such as Wnt11, ATF3, and IL1β, and influenced the crucial endogenous signalling pathways. The findings of this study suggest that PDA is a clinical translatable material that possess high potential in reducing scar contraction.Lei ChenZhiyong LiYongtai ZhengFei ZhouJingling ZhaoQiyi ZhaiZhaoqiang ZhangTianrun LiuYongming ChenShaohai QiKeAi Communications Co., Ltd.articleExtracellular matrixDermal analoguesScar contractionMacrophageAngiogenesisMaterials of engineering and construction. Mechanics of materialsTA401-492Biology (General)QH301-705.5ENBioactive Materials, Vol 10, Iss , Pp 236-246 (2022)
institution DOAJ
collection DOAJ
language EN
topic Extracellular matrix
Dermal analogues
Scar contraction
Macrophage
Angiogenesis
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
spellingShingle Extracellular matrix
Dermal analogues
Scar contraction
Macrophage
Angiogenesis
Materials of engineering and construction. Mechanics of materials
TA401-492
Biology (General)
QH301-705.5
Lei Chen
Zhiyong Li
Yongtai Zheng
Fei Zhou
Jingling Zhao
Qiyi Zhai
Zhaoqiang Zhang
Tianrun Liu
Yongming Chen
Shaohai Qi
3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
description Scar contraction frequently happens in patients with deep burn injuries. Hitherto, porcine dermal extracellular matrix (dECM) has supplied microenvironments that assist in wound healing but fail to inhibit scar contraction. To overcome this drawback, we integrate dECM into three-dimensional (3D)-printed dermal analogues (PDA) to prevent scar contraction. We have developed thermally gelled, non-rheologically modified dECM powder (dECMp) inks and successfully transformed them into PDA that was endowed with a micron-scale spatial structure. The optimal crosslinked PDA exhibited desired structure, good mechanical properties as well as excellent biocompatibility. Moreover, in vivo experiments demonstrated that PDA could significantly reduced scar contraction and improved cosmetic upshots of split thickness skin grafts (STSG) than the commercially available dermal templates and STSG along. The PDA has also induced an early, intense neovascularization, and evoked a type-2-like immune response. PDA's superior beneficial effects may attribute to their desired porous structure, the well-balanced physicochemical properties, and the preserved dermis-specific ECM cues, which collectively modulated the expression of genes such as Wnt11, ATF3, and IL1β, and influenced the crucial endogenous signalling pathways. The findings of this study suggest that PDA is a clinical translatable material that possess high potential in reducing scar contraction.
format article
author Lei Chen
Zhiyong Li
Yongtai Zheng
Fei Zhou
Jingling Zhao
Qiyi Zhai
Zhaoqiang Zhang
Tianrun Liu
Yongming Chen
Shaohai Qi
author_facet Lei Chen
Zhiyong Li
Yongtai Zheng
Fei Zhou
Jingling Zhao
Qiyi Zhai
Zhaoqiang Zhang
Tianrun Liu
Yongming Chen
Shaohai Qi
author_sort Lei Chen
title 3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
title_short 3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
title_full 3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
title_fullStr 3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
title_full_unstemmed 3D-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage M2 polarization
title_sort 3d-printed dermis-specific extracellular matrix mitigates scar contraction via inducing early angiogenesis and macrophage m2 polarization
publisher KeAi Communications Co., Ltd.
publishDate 2022
url https://doaj.org/article/b6fae460aa79463db07b5c6e92804fbf
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