Cytoskeletal activation of NHE1 regulates mechanosensitive cell volume adaptation and proliferation

Mammalian cells rapidly respond to environmental changes by altering transmembrane water and ion fluxes, changing cell volume. Contractile forces generated by actomyosin have been proposed to mechanically regulate cell volume. However, our findings reveal a different mechanism in adherent cells, where elevated actomyosin activity increases cell volume in normal-like cells (NIH 3T3 and others) through interaction with the sodium-hydrogen exchanger isoform 1 (NHE1). This leads to a slow secondary volume increase (SVI) following the initial regulatory volume decrease during hypotonic shock. The active cell response is further confirmed by intracellular alkalinization during mechanical stretch. Moreover, cytoskeletal activation of NHE1 during SVI deforms the nucleus, causing immediate transcriptomic changes and ERK-dependent growth inhibition. Notably, SVI and its associated changes are absent in many cancer cell lines or cells on compliant substrates with reduced actomyosin activity. Thus, actomyosin acts as a sensory element rather than a force generator during adaptation to environmental challenges.

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Publication Details

Journal
Cell Reports
Published
2024-11-22
DOI
https://doi.org/10.1016/j.celrep.2024.114992
Citations
9
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
2.93

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article

Cytoskeletal activation of NHE1 regulates mechanosensitive cell volume adaptation and proliferation

Qin Ni, Dingchang Lin, Sean X. Sun, Kaustav Bera et al.
9 citations
Cell Reports
Cellular Mechanics and Interactions
2.93
article

Cytoskeletal activation of NHE1 regulates mechanosensitive cell volume adaptation and proliferation

Qin Ni, Dingchang Lin, Sean X. Sun, Kaustav Bera, Κωνσταντίνος Κωνσταντόπουλος, Yizeng Li, Ana Carina Nogueira Vasconcelos, Gabriel Shatkin, Yichen Wang, Andrew P. Feinberg, Yuhan Yang, Zhuoxu Ge, Yuqing Yan, Yufei Wu, Anindya Sen, Jinyu Fu
article en
9 citations

Abstract

Mammalian cells rapidly respond to environmental changes by altering transmembrane water and ion fluxes, changing cell volume. Contractile forces generated by actomyosin have been proposed to mechanically regulate cell volume. However, our findings reveal a different mechanism in adherent cells, where elevated actomyosin activity increases cell volume in normal-like cells (NIH 3T3 and others) through interaction with the sodium-hydrogen exchanger isoform 1 (NHE1). This leads to a slow secondary volume increase (SVI) following the initial regulatory volume decrease during hypotonic shock. The active cell response is further confirmed by intracellular alkalinization during mechanical stretch. Moreover, cytoskeletal activation of NHE1 during SVI deforms the nucleus, causing immediate transcriptomic changes and ERK-dependent growth inhibition. Notably, SVI and its associated changes are absent in many cancer cell lines or cells on compliant substrates with reduced actomyosin activity. Thus, actomyosin acts as a sensory element rather than a force generator during adaptation to environmental challenges.

Cell ReportsVol. 43(12)
Binghamton University (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Sidney Kimmel Comprehensive Cancer Center (US)
National Science Foundation, Johns Hopkins University, Bloomberg Philanthropies, National Institutes of Health, National Institute of General Medical Sciences
Openalex Percentile: Top 9%
Cellular Mechanics and Interactions
2.93
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