压电1
炎症
细胞生物学
免疫系统
糖酵解
渗透(HVAC)
生物
趋化因子
串扰
趋化性
化学
免疫学
新陈代谢
生物化学
离子通道
材料科学
光学
物理
复合材料
受体
机械敏感通道
作者
Yingchao Xue,Elizabeth Winnicki,Zhaoxu Zhang,Inés López,Saifeng Wang,Charles Kirby,Sam Lee,Ang Li,Chaewon Lee,Hana Minsky,Kaitlin L. Williams,Yueh‐Hsun Yang,Ling He,Sashank Reddy,Luis A. Garza
标识
DOI:10.1038/s41467-025-62270-3
摘要
The skin has a remarkable ability to grow under constant stretch. Using a controlled tissue expansion system in mice, we identified an enhanced inflammatory-metabolic network in stretched skin via single-cell RNA sequencing, flow cytometry and spatial transcriptomics. Stretched epidermal cells exhibit heightened cellular crosstalk of CXCL, CCL, TNF, and TGF-β signaling. Additionally, skin expansion increases macrophage and monocyte infiltration in the skin while altering systemic immune cell profiles. Glycolysis-related genes, including Glut1 and Aldoa were significantly elevated. We hypothesize that Piezo1, a non-selective calcium-permeable cation channel, senses tension in stretched skin, driving these responses. The epidermal-Piezo1 loss-of-function animals show reduced skin growth, tissue weight, tissue thickness, macrophage infiltration, and glycolysis activity. Conversely, animals with a pharmacological Piezo1 gain of function exhibit an increase in these factors. Our findings highlight the coordinating role of Piezo1 for metabolic changes and immune cell infiltration in tension-induced skin growth.
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