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Microbial adhesion promotes Piezo1 activation to initiate innate immunity.

Created on 10 Sep 2026

Authors

Giulia Stucchi, Marco Galli, Stefano Cozzi, Anna Celant, Laura Marongiu, Giuseppe Rocca, Francesca Colnaghi, Maria Rita Chelazzi, Alessandra Polissi, Alessandra Maria Martorana, Giampiero Pietrocola, Marina Vai, Ivan Orlandi, Renato Ostuni, Simona Barresi, Angelo Lombardo, Metello Innocenti, Francesca Granucci

Published in

Nature immunology. Sep 09, 2026. Epub Sep 09, 2026.

Abstract

How mammals mount an effective immune response against infectious agents remains unresolved. Here we identify microbial adhesion to myeloid cells as a critical initiating event that precedes pattern recognition receptor (PRR) engagement. Using a skin infection model with pathogenic bacteria and fungi, we demonstrate that neutrophil recruitment occurs in two sequential phases. The early phase is PRR-independent and instead driven by microbial adhesion, which engages the mechanosensitive ion channel Piezo1 to promote leukotriene (LT)B4 production. Together with interleukin-1α, LTB4 induces CXCL1 release, triggering neutrophil infiltration via the same circuit at play during sterile inflammation. By contrast, the late phase is toll-like receptor (TLR)- and CXCL2-dependent, marking a transition to the canonical, pathogen-driven response. Our findings uncover microbial adhesion as a previously unrecognized danger signal that activates innate immunity via mechanotransduction, revealing a paradigm of how immune responses to infection are initiated.

PMID:
42717253
Bibliographic data and abstract were imported from PubMed on 10 Sep 2026.

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