Open AccessSingle‐Cell Mechanical Characterization of Human Macrophages
Author(s) -
Evers Tom M. J.,
Sheikhhassani Vahid,
Tang Huaqi,
Haks Mariëlle C.,
Ottenhoff Tom H. M.,
Mashaghi Alireza
Publication year - 2022
Publication title -
advanced nanobiomed research
Language(s) - English
Resource type - Journals
ISSN - 2699-9307
DOI - 10.1002/anbr.202100133
Subject(s) - macrophage , phagocytosis , microbiology and biotechnology , phenotype , motility , cell , immune system , granulocyte macrophage colony stimulating factor , function (biology) , biology , chemistry , immunology , in vitro , cytokine , biochemistry , gene
Macrophages remodel their mechanics during differentiation toward different subtypes and drastically adapt their shapes during phagocytosis or entry to inflamed tissues. Although these functions depend on cell mechanical properties, the mechanical behavior of macrophages is still poorly understood and accurate physiologically relevant data on basic mechanical properties of different macrophage subtypes are lacking almost entirely. By combining several complementary single‐cell force spectroscopy techniques, whole cell mechanics of M1 (differentiated by granulocyte macrophage colony‐stimulating factor [GM‐CSF]) and M2 (differentiated by macrophage colony‐stimulating factor [M‐CSF]) macrophages is systematically analyzed, and it is revealed that M2 macrophages exhibit solid‐like behavior, whereas M1 macrophages behave more fluid‐like. In addition, the findings indicate that M2 macrophages exhibit increased dynamic motility as compared to M1 macrophages, consistent with their mechanical phenotypes. The technology presented herein can be used to distinguish macrophage subtypes based on their mechanical phenotype, and suggests that mechanical properties of macrophages are linked to their immune function.