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Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology

Author

Listed:
  • Jeong-Ki Kim

    (Korea University)

  • Arghavan Louhghalam

    (University of Massachusetts Dartmouth)

  • Geonhui Lee

    (Korea University)

  • Benjamin W. Schafer

    (The Johns Hopkins University
    The John Hopkins University)

  • Denis Wirtz

    (The Johns Hopkins University
    The John Hopkins University
    The Johns Hopkins University
    The Johns Hopkins School of Medicine)

  • Dong-Hwee Kim

    (Korea University)

Abstract

The distinct spatial architecture of the apical actin cables (or actin cap) facilitates rapid biophysical signaling between extracellular mechanical stimuli and intracellular responses, including nuclear shaping, cytoskeletal remodeling, and the mechanotransduction of external forces into biochemical signals. These functions are abrogated in lamin A/C-deficient mouse embryonic fibroblasts that recapitulate the defective nuclear organization of laminopathies, featuring disruption of the actin cap. However, how nuclear lamin A/C mediates the ability of the actin cap to regulate nuclear morphology remains unclear. Here, we show that lamin A/C expressing cells can form an actin cap to resist nuclear deformation in response to physiological mechanical stresses. This study reveals how the nuclear lamin A/C-mediated formation of the perinuclear apical actin cables protects the nuclear structural integrity from extracellular physical disturbances. Our findings highlight the role of the physical interactions between the cytoskeletal network and the nucleus in cellular mechanical homeostasis.

Suggested Citation

  • Jeong-Ki Kim & Arghavan Louhghalam & Geonhui Lee & Benjamin W. Schafer & Denis Wirtz & Dong-Hwee Kim, 2017. "Nuclear lamin A/C harnesses the perinuclear apical actin cables to protect nuclear morphology," Nature Communications, Nature, vol. 8(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-02217-5
    DOI: 10.1038/s41467-017-02217-5
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