IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v15y2024i1d10.1038_s41467-024-52453-9.html
   My bibliography  Save this article

β2 integrins impose a mechanical checkpoint on macrophage phagocytosis

Author

Listed:
  • Alexander H. Settle

    (Memorial Sloan Kettering Cancer Center
    Memorial Sloan Kettering Cancer Center)

  • Benjamin Y. Winer

    (Memorial Sloan Kettering Cancer Center)

  • Miguel M. Jesus

    (Memorial Sloan Kettering Cancer Center
    Memorial Sloan Kettering Cancer Center)

  • Lauren Seeman

    (Memorial Sloan Kettering Cancer Center)

  • Zhaoquan Wang

    (Memorial Sloan Kettering Cancer Center
    Weill Cornell Graduate School of Medical Sciences)

  • Eric Chan

    (Memorial Sloan Kettering Cancer Center)

  • Yevgeniy Romin

    (Memorial Sloan Kettering Cancer Center)

  • Zhuoning Li

    (Memorial Sloan Kettering Cancer Center)

  • Matthew M. Miele

    (Memorial Sloan Kettering Cancer Center)

  • Ronald C. Hendrickson

    (Memorial Sloan Kettering Cancer Center
    Memorial Sloan Kettering Cancer Center
    University of Miami School of Medicine)

  • Daan Vorselen

    (Wageningen University & Research)

  • Justin S. A. Perry

    (Memorial Sloan Kettering Cancer Center
    Memorial Sloan Kettering Cancer Center
    Weill Cornell Graduate School of Medical Sciences)

  • Morgan Huse

    (Memorial Sloan Kettering Cancer Center
    Memorial Sloan Kettering Cancer Center
    Weill Cornell Graduate School of Medical Sciences)

Abstract

Phagocytosis is an intensely physical process that depends on the mechanical properties of both the phagocytic cell and its chosen target. Here, we employed differentially deformable hydrogel microparticles to examine the role of cargo rigidity in the regulation of phagocytosis by macrophages. Whereas stiff cargos elicited canonical phagocytic cup formation and rapid engulfment, soft cargos induced an architecturally distinct response, characterized by filamentous actin protrusions at the center of the contact site, slower cup advancement, and frequent phagocytic stalling. Using phosphoproteomics, we identified β2 integrins as critical mediators of this mechanically regulated phagocytic switch. Macrophages lacking β2 integrins or their downstream effectors, Talin1 and Vinculin, exhibited specific defects in phagocytic cup architecture and selective suppression of stiff cargo uptake. We conclude that integrin signaling serves as a mechanical checkpoint during phagocytosis to pair cargo rigidity to the appropriate mode of engulfment.

Suggested Citation

  • Alexander H. Settle & Benjamin Y. Winer & Miguel M. Jesus & Lauren Seeman & Zhaoquan Wang & Eric Chan & Yevgeniy Romin & Zhuoning Li & Matthew M. Miele & Ronald C. Hendrickson & Daan Vorselen & Justin, 2024. "β2 integrins impose a mechanical checkpoint on macrophage phagocytosis," Nature Communications, Nature, vol. 15(1), pages 1-20, December.
  • Handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52453-9
    DOI: 10.1038/s41467-024-52453-9
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-52453-9
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-52453-9?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Daan Vorselen & Yifan Wang & Miguel M. Jesus & Pavak K. Shah & Matthew J. Footer & Morgan Huse & Wei Cai & Julie A. Theriot, 2020. "Microparticle traction force microscopy reveals subcellular force exertion patterns in immune cell–target interactions," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
    2. Laetitia Weinhard & Giulia Bartolomei & Giulia Bolasco & Pedro Machado & Nicole L. Schieber & Urte Neniskyte & Melanie Exiga & Auguste Vadisiute & Angelo Raggioli & Andreas Schertel & Yannick Schwab &, 2018. "Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction," Nature Communications, Nature, vol. 9(1), pages 1-14, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Péter Berki & Csaba Cserép & Zsuzsanna Környei & Balázs Pósfai & Eszter Szabadits & Andor Domonkos & Anna Kellermayer & Miklós Nyerges & Xiaofei Wei & Istvan Mody & Araki Kunihiko & Heinz Beck & He Ka, 2024. "Microglia contribute to neuronal synchrony despite endogenous ATP-related phenotypic transformation in acute mouse brain slices," Nature Communications, Nature, vol. 15(1), pages 1-24, December.
    2. Wanjie Wu & Yingzhu He & Yujun Chen & Yiming Fu & Sicong He & Kai Liu & Jianan Y. Qu, 2024. "In vivo imaging in mouse spinal cord reveals that microglia prevent degeneration of injured axons," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    3. Max Adrian & Martin Weber & Ming-Chi Tsai & Caspar Glock & Olga I. Kahn & Lilian Phu & Tommy K. Cheung & William J. Meilandt & Christopher M. Rose & Casper C. Hoogenraad, 2023. "Polarized microtubule remodeling transforms the morphology of reactive microglia and drives cytokine release," Nature Communications, Nature, vol. 14(1), pages 1-20, December.
    4. I. Hristovska & M. Robert & K. Combet & J. Honnorat & J-C Comte & O. Pascual, 2022. "Sleep decreases neuronal activity control of microglial dynamics in mice," Nature Communications, Nature, vol. 13(1), pages 1-15, December.
    5. Fabrizio A. Pennacchio & Alessandro Poli & Francesca Michela Pramotton & Stefania Lavore & Ilaria Rancati & Mario Cinquanta & Daan Vorselen & Elisabetta Prina & Orso Maria Romano & Aldo Ferrari & Matt, 2024. "N2FXm, a method for joint nuclear and cytoplasmic volume measurements, unravels the osmo-mechanical regulation of nuclear volume in mammalian cells," Nature Communications, Nature, vol. 15(1), pages 1-10, December.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:15:y:2024:i:1:d:10.1038_s41467-024-52453-9. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.