自愈水凝胶
汞菁
螺吡喃
生物相容性
生物物理学
肽
细胞外基质
材料科学
细胞外
刚度
细胞命运测定
细胞
异构化
化学
纳米技术
自愈
弹性模量
组织工程
MyoD公司
寡肽
调制(音乐)
作者
Zhenhua Wu,Hao Kong,Junxiao Wang,Guan Jun,Meizhen Yin
标识
DOI:10.1002/adfm.202526641
摘要
Abstract Photo‐responsive peptide hydrogels are ideal for mimicking the extracellular matrix (ECM) with dynamic stiffness to regulate cellular behaviors. However, achieving reversible stiffness modulation without greatly altering gel composition or structure, which may interfere with stiffness‐dependent cell responses, remains challenging. Here, a bio‐inspired peptide hydrogel is reported, whose modulus can be reversibly regulated via a hydration‐mediated “water switch” upon light stimuli. Spiropyran (SP) units are integrated into DFYD‐based peptides to construct a co‐assembled hydrogel, with a low critical gelation concentration of 0.2 wt.%. In the zwitterionic, ring‐opened merocyanine (MC) state, the gel retained more water and remained soft. Upon visible light irradiation, MC/SP isomerization reduced polarity, expelled water from the gel, and increased stiffness. The gels exhibited excellent biocompatibility in both states and highlighted enhanced cell proliferation and differentiation through light‐controlled modulation of stiffness. This work provides a new strategy for constructing smart hydrogels for regenerative therapy applications.
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