Macrophage migration is differentially regulated by fibronectin and laminin through altered adhesion and myosin II localization.

Autor: Stinson MW; Uniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817., Liu S; Uniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817., Laurenson AJ; Uniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.; The Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD 20817., Rotty JD; Uniformed Services University of the Health Sciences, Department of Biochemistry, Bethesda, MD 20814.
Jazyk: angličtina
Zdroj: Molecular biology of the cell [Mol Biol Cell] 2024 Feb 01; Vol. 35 (2), pp. ar22. Date of Electronic Publication: 2023 Dec 13.
DOI: 10.1091/mbc.E23-04-0137
Abstrakt: Macrophages are indispensable for proper immune surveillance and inflammatory regulation. They also exhibit dramatic phenotypic plasticity and are highly responsive to their local microenvironment, which includes the extracellular matrix (ECM). This work demonstrates that two fibrous ECM glycoproteins, fibronectin (FN) and laminin (LAM), elicit distinct morphological and migratory responses from macrophages in two-dimensional environments. LAM 111 inhibits macrophage cell spreading, but drives them to migrate rapidly and less persistently compared with cells on FN. Differential integrin engagement and ROCK/myosin II organization helps explain why macrophages alter their morphology and migration character on these two ECM components. This study also demonstrates that LAM 111 exerts a suppressive effect toward FN, as macrophages plated on a LAM/FN mixture adopt a morphology and migratory character almost identical to LAM alone. This suggests that distinct responses can be initiated downstream of receptor-ECM engagement, and that one component of the microenvironment may affect the cell's ability to sense another. Overall, macrophages appear intrinsically poised to rapidly switch between distinct migratory characters based on their ECM environments. The role of ECM composition in dictating motile and inflammatory responses in three-dimensional and in vivo contexts warrants further study.
Databáze: MEDLINE