Journal of Molecular BiologyBiochemistryPeer-reviewed journal article
Human plastins are novel cytoskeletal pH sensors with a reduced F-actin bundling capacity at basic pH
Lucas A. RunyaniD, Elena KudryashovaiD, Richa AgrawaliD, Mubarik Mohamed, Dmitri S. KudryashoviD
Abstract
Intracellular pH (pHi) is a fundamental component of cell homeostasis. Controlled elevations in pHi precede and accompany cell polarization, cytokinesis, and directional migration. pH dysregulation contributes to cancer, neurodegenerative diseases, diabetes, and other metabolic disorders. While cytoskeletal rearrangements are crucial for these processes, only a few cytoskeletal proteins, namely Cdc42, cofilin, talin, cortactin, -actinin, and AIP1 have been documented as pH sensors. Here, we report that actin-bundling proteins plastin 2 (PLS2, aka LCP1) and plastin 3 (PLS3) respond to physiological scale pH fluctuations by a reduced F-actin bundling at alkaline pH. The inhibition of PLS2 actin-bundling activity at elevated pH stems from the reduced affinity of the N-terminal actin-binding domain (ABD1) to actin. In fibroblast cells, elevated cytosolic pH caused the dissociation of ectopically expressed PLS2 from actin structures, whereas acidic conditions promoted its tighter association with focal adhesions and stress fibers. We identified His207 as one of the pH-sensing residues whose mutation to Lys and Tyr reduces pH sensitivity by enhancing and inhibiting the bundling ability, respectively. Our results suggest that weaker actin bundling by plastin isoforms at alkaline pH favors higher dynamics of the actin cytoskeleton. Therefore, like other cytoskeleton pH sensors, plastins promote disassembly and faster dynamics of cytoskeletal components during cytokinesis and cell migration. Since both plastins are implemented in cancer, their pH sensitivity may contribute to the accelerated proliferation and enhanced invasive and metastatic potentials of cancer cells at alkaline pHi. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=152 SRC="FIGDIR/small/645573v1_ufig1.gif" ALT="Figure 1"> View larger version (69K): org.highwire.dtl.DTLVardef@18430a4org.highwire.dtl.DTLVardef@19584b1org.highwire.dtl.DTLVardef@13a8354org.highwire.dtl.DTLVardef@840dc3_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: human
- assay: proteomics
- research focus: cell signaling & trafficking
- approach: experimental assay
- Citations
- 3
- FWCI
- 1.50
- Field percentile
- top 20%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Allosteric Regulation of Human Plastins
C. Schwebach, E. Kudryashova, … D. S. KUDRYASHOV·bioRxiv·Dec 1, 2021
- Intracellular pH regulates beta-catenin with low pH increasing adhesion and signaling functions
B. J. Czowski, A. N. Marchi, K. A. White·bioRxiv·Mar 22, 2024
- Ventral Stress Fibers Induce Plasma Membrane Deformation in Human Fibroblasts
S. J. Ghilardi, M. S. Aronson, A. E. Sgro·bioRxiv·Mar 1, 2021
- A role for class I PAKs in the regulation of the excitability of the actin cytoskeleton.
Joe J. Tyler, Anthony C. Davidson, … Vassilis E. Koronakis·Journal of Cell SciencePeer-reviewed·Jun 15, 2025
- Tubulin C-terminal tails are pH sensors that regulate microtubule function
Allison M. Whited, Patrick Ryan DeLear, … Loren E. Hough·Journal of Biological ChemistryPeer-reviewed·Sep 25, 2026
- Stress pathway outputs are encoded by pH-dependent phase separation of its components.
Yuliia Didan, Milad Ghomlaghi, … Dominic C.H. Ng·Nature CommunicationsPeer-reviewed·Aug 5, 2024