Spatiotemporal dynamics of membrane surface charge regulates cell polarity and migration

• Published in: Nature cell biology Vol. 24; no. 10; pp. 1499 - 1515
• Main Authors: Banerjee, Tatsat, Biswas, Debojyoti, Pal, Dhiman Sankar, Miao, Yuchuan, Iglesias, Pablo A., Devreotes, Peter N.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.10.2022; Nature Publishing Group
• Subjects: 1-Phosphatidylinositol 3-kinase; 13/1; 13/106; 13/109; 13/44; 13/95; 14/19; 14/34; 14/35; 14/56; 14/63; 38/22; 38/23; 38/77; 631/57/2270; 631/80/84; 631/80/85; 631/80/86; 9/10; Actin; Actins - metabolism; Actuators; AKT protein; Biochemistry; Biomedical and Life Sciences; Cancer Research; Cell adhesion & migration; Cell Biology; Cell Membrane - metabolism; Cell migration; Cell Movement; Cell Polarity - physiology; Cell surface; Chemotactic Factors - metabolism; Computer applications; Cytoskeleton; Developmental Biology; Epidermal Growth Factor; Feedback; Feedback loops; Genetic analysis; Life Sciences; Localization; Mechanistic Target of Rapamycin Complex 2 - metabolism; Membranes; Molecular interactions; Phosphatidic acid; Phosphatidylinositol 3-Kinases - genetics; Phosphatidylinositol 3-Kinases - metabolism; Phosphatidylserine; Phosphatidylserines - metabolism; Phospholipids; Polarity; Proto-Oncogene Proteins c-akt - genetics; Proto-Oncogene Proteins c-akt - metabolism; Recruitment; Signal transduction; Signaling; Stem Cells; Surface charge; Zeta potential
• ISSN: 1465-7392; 1476-4679
• DOI: 10.1038/s41556-022-00997-7

During cell migration and polarization, numerous signal transduction and cytoskeletal components self-organize to generate localized protrusions. Although biochemical and genetic analyses have delineated many specific interactions, how the activation and localization of so many different molecules are spatiotemporally orchestrated at the subcellular level has remained unclear. Here we show that the regulation of negative surface charge on the inner leaflet of the plasma membrane plays an integrative role in the molecular interactions. Surface charge, or zeta potential, is transiently lowered at new protrusions and within cortical waves of Ras/PI3K/TORC2/F-actin network activation. Rapid alterations of inner leaflet anionic phospholipids—such as PI(4,5)P2, PI(3,4)P2, phosphatidylserine and phosphatidic acid—collectively contribute to the surface charge changes. Abruptly reducing the surface charge by recruiting positively charged optogenetic actuators was sufficient to trigger the entire biochemical network, initiate de novo protrusions and abrogate pre-existing polarity. These effects were blocked by genetic or pharmacological inhibition of key signalling components such as AKT and PI3K/TORC2. Conversely, increasing the negative surface charge deactivated the network and locally suppressed chemoattractant-induced protrusions or subverted EGF-induced ERK activation. Computational simulations involving excitable biochemical networks demonstrated that slight changes in feedback loops, induced by recruitment of the charged actuators, could lead to outsized effects on system activation. We propose that key signalling network components act on, and are in turn acted upon, by surface charge, closing feedback loops, which bring about the global-scale molecular self-organization required for spontaneous protrusion formation, cell migration and polarity establishment. Banerjee et al. detail the spatial and temporal dynamics of the surface charge on the inner leaflet of the plasma membrane and show that these dynamics are necessary and sufficient to regulate signalling pathways mediating cell migration and polarity.