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NEUROREGULATION AND MOTILITY

Direct association of calponin with specific domains of PKC-

Department of Pediatrics-Gastroenterology, University of Michigan Medical Center, Ann Arbor, Michigan

Submitted 30 July 2008 ; accepted in final form 17 October 2008

Calponin contributes to the regulation of smooth muscle contraction through its interaction with F-actin and inhibition of the actin-activated Mg-ATPase activity of phosphorylated myosin. Previous studies have shown that the contractile agonist acetylcholine induced a direct association of translocated calponin and PKC- in the membrane. In the present study, we have determined the domain of PKC- involved in direct association with calponin. In vitro binding assay was carried out by incubating glutathione S-transferase-calponin aa 92-229 with His-tagged proteins of individual domains and different combinations of domains of PKC-. Calponin was found to bind directly to the full-length PKC-. Calponin bound to C2 and C4 domains but not to C1 and C3 domains of PKC-. When incubated with proteins of different combination of domains, calponin bound to C2-C3, C3-C4, and C2-C3-C4 but not to C1-C2 or C1-C2-C3. To determine whether these in vitro bindings mimic the in vivo associations, and in vivo binding assay was performed by transfecting colonic smooth muscle cells with His-tagged proteins of individual domains and different combinations of domains of PKC-. Coimmunoprecipitation of calponin with His-tagged truncated forms of PKC- showed that C1-C2, C1-C2-C3, C2-C3, and C3-C4 did not associate with calponin. Calponin associated only with full-length PKC- and with C2-C3-C4 in cells in the resting state, and this association increased upon stimulation with acetylcholine. These data suggest that calponin bound to fragments that may mimic the active form of PKC- and that the functional association of PKC- with calponin requires both C2 and C4 domains during contraction of colonic smooth muscle cells.

tropomyosin; smooth muscle; contraction; cytoskeleton; signaling