期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 281, 期 20, 页码 14015-14025出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M600433200
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资金
- NCRR NIH HHS [RR-017353] Funding Source: Medline
- NHLBI NIH HHS [HL-72989] Funding Source: Medline
L-type, voltage-gated Ca2+ channels (CaL) play critical roles in brain and muscle cell excitability. Here we show that currents through heterologously expressed neuronal and smooth muscle CaL channel isoforms are acutely potentiated following alpha 5 beta 1 integrin activation. Only the alpha(1C) pore-forming channel subunit is critical for this process. Truncation and site-directed mutagenesis strategies reveal that regulation of Cav1.2 by alpha 5 beta 1 integrin requires phosphorylation of alpha(1C) C-terminal residues Ser(1901) and Tyr(2122). These sites are known to be phosphorylated by protein kinase A(PKA) and c-Src, respectively, and are conserved between rat neuronal (Cav1.2c) and smooth muscle (Cav1.2b) isoforms. Kinase assays are consistent with phosphorylation of these two residues by PKA and c-Src. Following alpha 5 beta 1 integrin activation, native CaL channels in rat arteriolar smooth muscle exhibit potentiation that is completely blocked by combined PKA and Src inhibition. Our results demonstrate that integrin-ECM interactions are a common mechanism for the acute regulation of CaL channels in brain and muscle. These findings are consistent with the growing recognition of the importance of integrin-channel interactions in cellular responses to injury and the acute control of synaptic and blood vessel function.
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