Caveolin-1α regulates primary cilium length by controlling RhoA GTPase activity

• Published in: Scientific reports 2019-02, Vol.9 (1), p.1116, Article 1116
• Main Authors: Rangel, Laura, Bernabé-Rubio, Miguel, Fernández-Barrera, Jaime, Casares-Arias, Javier, Millán, Jaime, Alonso, Miguel A., Correas, Isabel
• Format: Article
• Language: English
• Subjects: 14; 14/19; 14/28; 14/35; 42; 42/109; 42/89; 631/80/642; 631/80/85; Actin; Actin Cytoskeleton - metabolism; Animals; Biosynthesis; Caveolae; Caveolin; Caveolin 1 - genetics; Caveolin 1 - metabolism; Caveolin-1; Cell cycle; Cell lines; Centrosome - metabolism; Cilia; Cilia - metabolism; Cloning; Cytoskeleton; Dogs; Formins - metabolism; Gene Expression Regulation; Gene Knockout Techniques; Gene Silencing; Growth factors; Guanosine triphosphatases; Humanities and Social Sciences; Humans; Invaginations; Isoforms; Madin Darby Canine Kidney Cells; Membranes; Mice; Microscopy; multidisciplinary; Protein Isoforms - genetics; Protein Isoforms - metabolism; Proteins; rab GTP-Binding Proteins - metabolism; rho-Associated Kinases - metabolism; rhoA GTP-Binding Protein - metabolism; RhoA protein; Rocks; Science; Science (multidisciplinary); Signal transduction; Structure-function relationships
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-018-38020-5

The primary cilium is a single non-motile protrusion of the plasma membrane of most types of mammalian cell. The structure, length and function of the primary cilium must be tightly controlled because their dysfunction is associated with disease. Caveolin 1 (Cav1), which is best known as a component of membrane invaginations called caveolae, is also present in non-caveolar membrane domains whose function is beginning to be understood. We show that silencing of α and β Cav1 isoforms in different cell lines increases ciliary length regardless of the route of primary ciliogenesis. The sole expression of Cav1α, which is distributed at the apical membrane, restores normal cilium size in Cav1 KO MDCK cells. Cells KO for only Cav1α, which also show long cilia, have a disrupted actin cytoskeleton and reduced RhoA GTPase activity at the apical membrane, and a greater accumulation of Rab11 vesicles at the centrosome. Subsequent experiments showed that DIA1 and ROCK help regulate ciliary length. Since MDCK cells lack apical caveolae, our results imply that non-caveolar apical Cav1α is an important regulator of ciliary length, exerting its effect via RhoA and its effectors, ROCK and DIA1.