Actin nano-architecture of phagocytic podosomes

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作者
J. Cody Herron
Shiqiong Hu
Takashi Watanabe
Ana T. Nogueira
Bei Liu
Megan E. Kern
Jesse Aaron
Aaron Taylor
Michael Pablo
Teng-Leong Chew
Timothy C. Elston
Klaus M. Hahn
机构
[1] University of North Carolina at Chapel Hill,Curriculum in Bioinformatics and Computational Biology
[2] University of North Carolina at Chapel Hill,Computational Medicine Program
[3] University of North Carolina at Chapel Hill,Department of Pharmacology, School of Medicine
[4] University of North Carolina at Chapel Hill,Department of Physics and Astronomy
[5] Howard Hughes Medical Institute Janelia Research Campus,Advanced Imaging Center
[6] University of North Carolina at Chapel Hill,Department of Chemistry
[7] University of North Carolina at Chapel Hill,Program in Molecular and Cellular Biophysics
[8] Fujita Health University,Division of Gene Regulation, Cancer Center
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Podosomes are actin-enriched adhesion structures important for multiple cellular processes, including migration, bone remodeling, and phagocytosis. Here, we characterize the structure and organization of phagocytic podosomes using interferometric photoactivated localization microscopy, a super-resolution microscopy technique capable of 15–20 nm resolution, together with structured illumination microscopy and localization-based super-resolution microscopy. Phagocytic podosomes are observed during frustrated phagocytosis, a model in which cells attempt to engulf micropatterned IgG antibodies. For circular patterns, this results in regular arrays of podosomes with well-defined geometry. Using persistent homology, we develop a pipeline for semi-automatic identification and measurement of podosome features. These studies reveal an hourglass shape of the podosome actin core, a protruding knob at the bottom of the core, and two actin networks extending from the core. Additionally, the distributions of paxillin, talin, myosin II, α-actinin, cortactin, and microtubules relative to actin are characterized.
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