The University of Chicago, Ben May Department for Cancer Research, Chicago, IL, 60637, USA.
Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, School of Chemistry and Molecular Engineering, East China University of Science & Technology, 130 # Meilong Road, Shanghai, 200237, China.
Nat Commun. 2021 Mar 15;12(1):1670. doi: 10.1038/s41467-021-21964-0.
Effective healing of skin wounds is essential for our survival. Although skin has strong regenerative potential, dysfunctional and disfiguring scars can result from aberrant wound repair. Skin scarring involves excessive deposition and misalignment of ECM (extracellular matrix), increased cellularity, and chronic inflammation. Transforming growth factor-β (TGFβ) signaling exerts pleiotropic effects on wound healing by regulating cell proliferation, migration, ECM production, and the immune response. Although blocking TGFβ signaling can reduce tissue fibrosis and scarring, systemic inhibition of TGFβ can lead to significant side effects and inhibit wound re-epithelization. In this study, we develop a wound dressing material based on an integrated photo-crosslinking strategy and a microcapsule platform with pulsatile release of TGF-β inhibitor to achieve spatiotemporal specificity for skin wounds. The material enhances skin wound closure while effectively suppressing scar formation in murine skin wounds and large animal preclinical models. Our study presents a strategy for scarless wound repair.
皮肤创伤的有效愈合对我们的生存至关重要。尽管皮肤具有很强的再生潜力,但异常的伤口修复会导致功能失调和毁容性的疤痕。皮肤疤痕涉及细胞外基质(ECM)的过度沉积和排列紊乱、细胞增多和慢性炎症。转化生长因子-β(TGFβ)信号通过调节细胞增殖、迁移、ECM 产生和免疫反应,对伤口愈合发挥多效作用。虽然阻断 TGFβ 信号可以减少组织纤维化和疤痕形成,但 TGFβ 的全身性抑制会导致严重的副作用,并抑制伤口再上皮化。在这项研究中,我们开发了一种基于集成光交联策略和具有 TGF-β 抑制剂脉冲释放的微胶囊平台的伤口敷料材料,以实现皮肤伤口的时空特异性。该材料在促进皮肤伤口闭合的同时,有效抑制了小鼠皮肤伤口和大动物临床前模型中的疤痕形成。我们的研究提出了一种无疤痕伤口修复的策略。