Direction of actin flow dictates integrin LFA-1 orientation during leukocyte migration
Direction of actin flow dictates integrin LFA-1 orientation during leukocyte migration
Date
2017-12-11
Authors
Nordenfelt, Pontus
Moore, Travis I.
Mehta, Shalin B.
Kalappurakkal, Joseph Mathew
Swaminathan, Vinay
Koga, Nobuyasu
Lambert, Talley J.
Baker, David
Waters, Jennifer C.
Oldenbourg, Rudolf
Tani, Tomomi
Mayor, Satyajit
Waterman, Clare M.
Springer, Timothy
Moore, Travis I.
Mehta, Shalin B.
Kalappurakkal, Joseph Mathew
Swaminathan, Vinay
Koga, Nobuyasu
Lambert, Talley J.
Baker, David
Waters, Jennifer C.
Oldenbourg, Rudolf
Tani, Tomomi
Mayor, Satyajit
Waterman, Clare M.
Springer, Timothy
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DOI
10.1038/s41467-017-01848-y
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Keywords
Actin
Integrin signalling
Integrins
Molecular imaging
Polarization microscopy
Integrin signalling
Integrins
Molecular imaging
Polarization microscopy
Abstract
Integrin αβ heterodimer cell surface receptors mediate adhesive interactions that provide traction for cell migration. Here, we test whether the integrin, when engaged to an extracellular ligand and the cytoskeleton, adopts a specific orientation dictated by the direction of actin flow on the surface of migrating cells. We insert GFP into the rigid, ligand-binding head of the integrin, model with Rosetta the orientation of GFP and its transition dipole relative to the integrin head, and measure orientation with fluorescence polarization microscopy. Cytoskeleton and ligand-bound integrins orient in the same direction as retrograde actin flow with their cytoskeleton-binding β-subunits tilted by applied force. The measurements demonstrate that intracellular forces can orient cell surface integrins and support a molecular model of integrin activation by cytoskeletal force. Our results place atomic, Å-scale structures of cell surface receptors in the context of functional and cellular, μm-scale measurements.
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© The Author(s), 2017. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Nature Communications 8 (2017): 2047, doi:10.1038/s41467-017-01848-y.
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Nature Communications 8 (2017): 2047