Natural polymeric and peptide-loaded composite wound dressings for scar prevention AITranslate
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Highlights • Genipin-crosslinked carboxymethyl chitosan, ..-poly(glutamic acid), and anti-fibrotic polypeptide (AF38Pep) were developed. • Wound dressings for healing and scar prevention (HSP) selectively inhibited myofibroblasts and keloid fibroblasts. • Anti-fibrotic effects of HSP included the inhibited gene expression of collagens and focal adhesion mediators. • HSP achieved scar-attenuated dermal regeneration in full-thickness dermal excision hypertrophic scar models. • HSP had facile fabrication and compatibility with long-term storage combined with idealistic wound dressing properties. Excessive or hypertrophic scarring after skin trauma can bring substantial psychological and socioeconomic burden. Achievement of attenuated scarring during wound repair remains a major clinical challenge. To limit pathological healing whilst attaining physiological restoration of skin integrity and function at wound sites, therapies should effectively reduce activity of scar-forming myofibroblasts without impeding normal granulation tissue formation by fibroblasts. Here, we developed an innovative wound dressing, prepared from genipin crosslinked hydrogel networks of carboxymethyl chitosan (CMCS), poly-γ-glutamic acid (γ-PGA) and anti-fibrotic polypeptide (AF38Pep). The composite wound dressing for healing and scar prevention (HSP) exhibited appropriate physicochemical, biocompatible, and wound dressing properties; while selectively inhibiting the proliferation, migration, and activity of pro-fibrotic cell phenotypes. RNA-Seq data revealed that wound dressings suppressed genes related to the focal adhesion pathway in heterograft keloid fibroblasts, and this was further attenuated by inclusion of AF38Pep. Furthermore, in vivo experiments in full-thickness dermal excision and hypertrophic scar models indicated that HSP promoted reduced-scar wound healing, as evidenced by attenuated inflammation; inhibition of fibroblast to myofibroblast differentiation; facilitation of distinct skin appendage regeneration; enhancement of vascularization; and regulation of favorable collagen deposition and distribution. Taken together, HSP wound dressings demonstrated multifunctional properties that supports their suitability as a candidate therapeutic option for anti-scarring skin repair. Graphical abstract Download : Download high-res image (299KB) Download : Download full-size image
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DOI:https://doi.org/10.1016/j.apmt.2021.101186
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Highlights • Genipin-crosslinked carboxymethyl chitosan, ..-poly(glutamic acid), and anti-fibrotic polypeptide (AF38Pep) were developed. • Wound dressings for healing and scar prevention (HSP) selectively inhibited myofibroblasts and keloid fibroblasts. • Anti-fibrotic effects of HSP included the inhibited gene expression of collagens and focal adhesion mediators. • HSP achieved scar-attenuated dermal regeneration in full-thickness dermal excision hypertrophic scar models. • HSP had facile fabrication and compatibility with long-term storage combined with idealistic wound dressing properties. Excessive or hypertrophic scarring after skin trauma can bring substantial psychological and socioeconomic burden. Achievement of attenuated scarring during wound repair remains a major clinical challenge. To limit pathological healing whilst attaining physiological restoration of skin integrity and function at wound sites, therapies should effectively reduce activity of scar-forming myofibroblasts without impeding normal granulation tissue formation by fibroblasts. Here, we developed an innovative wound dressing, prepared from genipin crosslinked hydrogel networks of carboxymethyl chitosan (CMCS), poly-γ-glutamic acid (γ-PGA) and anti-fibrotic polypeptide (AF38Pep). The composite wound dressing for healing and scar prevention (HSP) exhibited appropriate physicochemical, biocompatible, and wound dressing properties; while selectively inhibiting the proliferation, migration, and activity of pro-fibrotic cell phenotypes. RNA-Seq data revealed that wound dressings suppressed genes related to the focal adhesion pathway in heterograft keloid fibroblasts, and this was further attenuated by inclusion of AF38Pep. Furthermore, in vivo experiments in full-thickness dermal excision and hypertrophic scar models indicated that HSP promoted reduced-scar wound healing, as evidenced by attenuated inflammation; inhibition of fibroblast to myofibroblast differentiation; facilitation of distinct skin appendage regeneration; enhancement of vascularization; and regulation of favorable collagen deposition and distribution. Taken together, HSP wound dressings demonstrated multifunctional properties that supports their suitability as a candidate therapeutic option for anti-scarring skin repair. Graphical abstract Download : Download high-res image (299KB) Download : Download full-size image
quote
| GB/T 7714-2015 | [1] Lin Zhang, Yifan Tai, Xiangsheng Liu, et al. Applied Materials Today, 2021(25). DOI:10.1016/j.apmt.2021.101186. |
| MLA | [1] Lin Zhang, et al., Applied Materials Today, no. 25, 2021, https://doi.org/10.1016/j.apmt.2021.101186. |
| APA | [1] Lin Zhang, Yifan Tai, Xiangsheng Liu, Yufei Liu, Yunsheng Dong, Yujie Liu, Chao Yang, Deling Kong, Chunxiao Qi, Shufang Wang, & Adam C. Midgley. (2021). Applied Materials Today(25). https://doi.org/10.1016/j.apmt.2021.101186 |
| IEEE | [1] Lin Zhang, Yifan Tai, Xiangsheng Liu, Yufei Liu, Yunsheng Dong, Yujie Liu, Chao Yang, Deling Kong, Chunxiao Qi, Shufang Wang, and Adam C. Midgley, Applied Materials Today, no. 25, 2021, doi: 10.1016/j.apmt.2021.101186. keywords: {Natural materials;Polymeric hydrogel;Composite wound dressing;Wound healing;Fibrosis;Antiscarring;Hypertrophic scarring} |
