Clostridium difficile toxin B inhibits carbachol-induced force and myosin light chain phosphorylation in guinea-pig smooth muscle: role of Rho proteins

摘要

class="enumerated" style="list-style-type:decimal">Clostridium difficile toxin B glucosylates the Ras-related low molecular mass GTPases of the Rho subfamily thereby inactivating them. In the present report, toxin B was applied as a tool to test whether Rho proteins participate in the carbachol-induced increase in the Ca²⁺ sensitivity of force and myosin light chain (MLC) phosphorylation in intact intestinal smooth muscle.Small strips of the longitudinal muscle of guinea-pig small intestine were incubated in toxin B (40 ng ml⁻¹) overnight. Carbachol-induced force and intracellular [Ca²⁺], and, in a separate series, force and MLC phosphorylation, were determined.Carbachol induced a biphasic contraction: an initial rapid increase in force (peak 1) followed by a partial relaxation and a second delayed increase in force (peak 2). The peak of the Ca²⁺ signal measured with fura-2 preceded peak 1 of force and then declined to a lower suprabasal steady-state level. Peak 2 was not associated with a significant increase in [Ca²⁺]. Toxin B nearly completely inhibited peak 2 while peak 1 was not significantly inhibited. Toxin B had no effect on the Ca²⁺ transient.In control strips, MLC phosphorylation at peak 2 was 27.7 %, which was significantly higher than the resting value (18.6 %). The inhibition of the second, delayed, rise in force induced by toxin B was associated with complete inhibition of the increase in MLC phosphorylation. The resting MLC phosphorylation was not significantly different from that of the control strips.The initial increase in MLC phosphorylation determined 3 s after exposure to carbachol was 54 % in the control strips. Toxin B also inhibited this initial phosphorylation peak despite the fact that the Ca²⁺ transient and the initial increase in force were not inhibited by toxin B. This suggests that Rho proteins play an important role in setting the balance between MLC phosphorylation and dephosphorylation reactions even at high levels of intracellular Ca²⁺.These findings are consistent with the hypothesis that the delayed rise in force elicited by carbachol is due to an increase in the Ca²⁺ sensitivity of MLC phosphorylation mediated by Rho proteins.