Differential Regulation of Hemichannels and Gap Junction Channels by RhoA GTPase and Actin Cytoskeleton: A Comparative Analysis of Cx43 and Cx26

• Published in: International journal of molecular sciences 2024-07, Vol.25 (13), p.7246
• Main Authors: Jara, Oscar, Maripillán, Jaime, Momboisse, Fanny, Cárdenas, Ana María, García, Isaac E, Martínez, Agustín D
• Format: Article
• Language: English
• Subjects: Actin; Actin Cytoskeleton - metabolism; Actins - metabolism; Animals; Cell Membrane - metabolism; Comparative analysis; Connexin 26 - metabolism; Connexin 43 - metabolism; connexin trafficking; cytochalasin-B; Cytoskeleton; G proteins; gap junction channel regulation; Gap Junctions - metabolism; hemichannels; Humans; Membrane proteins; Permeability; Photographic industry; Plasma; Polymerization; Proteins; rhoA GTP-Binding Protein - metabolism; small GTPase; Somatotropin
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms25137246

Connexins (Cxs) are transmembrane proteins that assemble into gap junction channels (GJCs) and hemichannels (HCs). Previous researches support the involvement of Rho GTPases and actin microfilaments in the trafficking of Cxs, formation of GJCs plaques, and regulation of channel activity. Nonetheless, it remains uncertain whether distinct types of Cxs HCs and GJCs respond differently to Rho GTPases or changes in actin polymerization/depolymerization dynamics. Our investigation revealed that inhibiting RhoA, a small GTPase that controls actin polymerization, or disrupting actin microfilaments with cytochalasin B (Cyto-B), resulted in reduced GJCs plaque size at appositional membranes and increased transport of HCs to non-appositional plasma membrane regions. Notably, these effects were consistent across different Cx types, since Cx26 and Cx43 exhibited similar responses, despite having distinct trafficking routes to the plasma membrane. Functional assessments showed that RhoA inhibition and actin depolymerization decreased the activity of Cx43 GJCs while significantly increasing HC activity. However, the functional status of GJCs and HCs composed of Cx26 remained unaffected. These results support the hypothesis that RhoA, through its control of the actin cytoskeleton, facilitates the transport of HCs to appositional cell membranes for GJCs formation while simultaneously limiting the positioning of free HCs at non-appositional cell membranes, independently of Cx type. This dynamic regulation promotes intercellular communications and reduces non-selective plasma membrane permeability through a Cx-type dependent mechanism, whereby the activity of Cx43 HCs and GJCs are differentially affected but Cx26 channels remain unchanged.