Actin nano-architecture of phagocytic podosomes

被引:9
|
作者
Herron, J. Cody [1 ,2 ]
Hu, Shiqiong [3 ]
Watanabe, Takashi [3 ,8 ]
Nogueira, Ana T. [3 ]
Liu, Bei [3 ]
Kern, Megan E. [4 ]
Aaron, Jesse [5 ]
Taylor, Aaron [5 ]
Pablo, Michael [6 ,7 ]
Chew, Teng-Leong [5 ]
Elston, Timothy C. [1 ,2 ,3 ]
Hahn, Klaus M. [2 ,3 ]
机构
[1] Univ N Carolina, Curriculum Bioinformat & Computat Biol, Chapel Hill, NC 27515 USA
[2] Univ N Carolina, Computat Med Program, Chapel Hill, NC 27515 USA
[3] Univ N Carolina, Dept Pharmacol, Sch Med, Chapel Hill, NC 27515 USA
[4] Univ N Carolina, Dept Phys & Astron, Chapel Hill, NC USA
[5] Howard Hughes Med Inst, Adv Imaging Ctr, Janelia Res Campus, Ashburn, VA USA
[6] Univ N Carolina, Dept Chem, Chapel Hill, NC USA
[7] Univ N Carolina, Program Mol & Cellular Biophys, Chapel Hill, NC USA
[8] Fujita Hlth Univ, Canc Ctr, Div Gene Regulat, Toyoake, Aichi, Japan
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
SELF-ORGANIZATION; CELL; PROTEIN; DYNAMICS; FLUOROPHORES; OSTEOCLASTS; RING;
D O I
10.1038/s41467-022-32038-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Podosomes are actin structures important in multiple cell functions. Here, the authors use iPALM microscopy to reveal an "hourglass" shape of the podosome actin core, a protruding "knob" at the bottom of the core, and two actin networks extending from it. 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, alpha-actinin, cortactin, and microtubules relative to actin are characterized.
引用
收藏
页数:16
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