Epidermal stem cells control periderm injury repair via matrix-driven specialization of intercellular junctions
Year: 2025
Type: article
Abstract: Epidermal stem cells interact with the extracellular matrix (ECM) to regulate their differentiation and maintain skin architecture. Here, we demonstrate a role for basal epidermal stem cells (BECs)-ECM interaction in regulating adhesion molecules expressed by the periderm-the superficial epidermal cells (SECs) of the embryonic bilayered skin. Using the developing zebrafish fin fold, we identify BECs form distinct regions of collagen- versus laminin- enriched basement membranes through integrin-mediated adhesions. Mechanistically, collagen-associated BECs form desmosomes and adherens junctions (AJs) with SECs while laminin-associated BECs display reduced desmosomes but sustain AJs and actomyosin expression with SECs. Notably, we show both in vivo and in a bilayered human keratinocyte model, that laminin, compared to collagen, is sufficient to repress desmosome formation while sustaining AJs specifically at the interlayer cell contacts. In vivo, laminin deficiency enhances desmosome expression across layers and impairs the wound-healing capacity of SECs. This defect was partially rescued by genetic reduction of the desmosome protein Desmoplakin-1a, highlighting the role of ECM-dependent junctional specialization in mediating differences in SEC injury response. Overall, our findings identify that stem cells, through their matrix, establish specialized junctions in the overlying stratified epithelium, which contribute to skin healing properties.
Source: Nature Communications
Authors: Helen Mengze He, Liana C. Boraas, Jon M. Bell, Xiangyu Gong, Sophia L. Iannaccone, Zhang Wen, Michael Mak, Marina Carlson, Kaelyn Sumigray, Stefania Nicoli
Institutions: Yale University, Stony Brook University
Language: English
Subfield: Cell Biology
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $6,990
Awards: G1500780118, G1535566005, The hidden life of mRNAs: a non-coding role as sensors of endothelial cells mechanotransduction, G3257633638, miRNA-regulation at focal adhesions establishes vascular mechanohomeostasis, G437767537, G5216011792, Mechanics of mammalian morphogenesis, G713706486, G7786139779, Dynamic Cell-Matrix Interactions Dictate Thoracic Aortopathy, TRANSFER GRANT: Systems Biophysics of Multiscale State Transitions in Cells and Tissues
OpenAlex ID: W4415025127
