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Updated: May 10, 2025

Engineering a Bilayered Hydrogel to Control ASC Differentiation
Published on: May 25, 2012
SHP099-containing multi-targeting hydrogel promotes rapid skin reconstruction through modulating a variety of cells
Zhixiao Liu1, Lei Chen2, Bingbing Hao1
1Department of Histology and Embryology, Basic Medical College, Naval Medical University, Shanghai, China.
Introduction:
Adult wound scarring result in functional skin deficits. However, the development of effective measures to modulate the entire wound healing to encourage the skin function reconstruction is still a clinical challenge, as multiple cells are involved in wound healing hierarchically. Hydrogel scaffolds with long-lasting local release provide new insights into the clinical relevance of entire wound healing.
Methods:
Herein, a multi-targeting hydrogel loaded with SHP099 (Gel-SHP) is designed to modulate multiple cells during wound repair.
Results:
Our results show that Gel-SHP promotes rapid reconstruction of wound skin by modulating macrophages in the inflammatory stage, fibroblasts in the regeneration stage and smooth muscle cells in the remodelling stage. Gel-SHP could increase M2 macrophage differentiation and remodel the dermal shell of hair follicles through in situ release. Moreover, Gel-SHP may modulate myofibroblasts to promote wound contraction through SHP099-scaffold synergistic interactions.
Discussion:
Our results provide new insights into the design of functional hydrogels for tissue regeneration applications. Gel-SHP as a promising tool could provide new clues and new research paradigms for future studies and understanding of the wound healing process and dermal shell formation.

