Actin filament disruption inhibits L-type Ca(2+) channel current in cultured vascular smooth muscle cells

• Published in: American Journal of Physiology: Cell Physiology 2000-08, Vol.279 (2), p.C480-C487
• Main Authors: Nakamura, M, Sunagawa, M, Kosugi, T, Sperelakis, N
• Format: Article
• Language: English
• Subjects: Actins - drug effects; Actins - metabolism; Animals; Aorta - drug effects; Aorta - metabolism; Calcium Channels, L-Type - drug effects; Calcium Channels, L-Type - metabolism; Cells, Cultured; Colchicine - pharmacology; Cytochalasin D - pharmacology; Gout Suppressants - pharmacology; Microtubules - drug effects; Microtubules - metabolism; Muscle, Smooth, Vascular - drug effects; Muscle, Smooth, Vascular - metabolism; Nucleic Acid Synthesis Inhibitors - pharmacology; Rats
• ISSN: 0363-6143
• DOI: 10.1152/ajpcell.2000.279.2.c480

To clarify interactions between the cytoskeleton and activity of L-type Ca(2+) (Ca(L)) channels in vascular smooth muscle (VSM) cells, we investigated the effect of disruption of actin filaments and microtubules on the L-type Ca(2+) current [I(Ba(L))] of cultured VSM cells (A7r5 cell line) using whole cell voltage clamp. The cells were exposed to each disrupter for 1 h and then examined electrophysiologically and morphologically. Results of immunostaining using anti-alpha-actin and anti-alpha-tubulin antibodies showed that colchicine disrupted both actin filaments and microtubules, cytochalasin D disrupted only actin filaments, and nocodazole disrupted only microtubules. I(Ba(L)) was greatly reduced in cells that were exposed to colchicine or cytochalasin D but not to nocodazole. Colchicine even inhibited I(Ba(L)) by about 40% when the actin filaments were stabilized by phalloidin or when the cells were treated with phalloidin plus taxol to stabilize both cytoskeletal components. These results suggest that colchicine must also cause some inhibition of I(Ba(L)) due to another unknown mechanism, e.g., a direct block of Ca(L) channels. In summary, actin filament disruption of VSM cells inhibits Ca(L) channel activity, whereas disrupting the microtubules does not.