# SHP099-containing multi-targeting hydrogel promotes rapid skin reconstruction through modulating a variety of cells

**Authors:** Zhixiao Liu, Lei Chen, Bingbing Hao, Yijin Hou, Chuan Lv, Yuanjie Zhu, Chaofeng Han

PMC · DOI: 10.3389/fbioe.2025.1564827 · Frontiers in Bioengineering and Biotechnology · 2025-04-07

## TL;DR

A hydrogel containing SHP099 helps speed up skin healing by influencing different types of cells at various stages of wound repair.

## Contribution

A novel multi-targeting hydrogel loaded with SHP099 is developed to modulate multiple cell types during wound healing.

## Key findings

- Gel-SHP promotes rapid wound skin reconstruction by modulating macrophages, fibroblasts, and smooth muscle cells.
- Gel-SHP increases M2 macrophage differentiation and remodels the dermal shell of hair follicles.
- Gel-SHP synergistically modulates myofibroblasts to promote wound contraction.

## Abstract

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.

Herein, a multi-targeting hydrogel loaded with SHP099 (Gel-SHP) is designed to modulate multiple cells during wound repair.

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.

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.

## Full-text entities

- **Genes:** NR0B2 (nuclear receptor subfamily 0 group B member 2) [NCBI Gene 8431] {aka SHP, SHP1}
- **Diseases:** skin deficits (MESH:D012871), inflammatory (MESH:D007249)
- **Chemicals:** SHP099 (MESH:C000609471)

## Full text

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## Figures

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## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12009829/full.md

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Source: https://tomesphere.com/paper/PMC12009829