Key result
Schistosoma mansoni muscle fibres feature a prominent Ca2+-activated K+ channel with ~195 pS conductance.
Why the study?
Muscle cells isolated from Schistosoma mansoni were studied to characterize their ionic conductances and identify Ca2+-activated K+ channels.
Answers are grounded in this paper and cite their sources.
May represent a novel anthelmintic target; leaves open whether channel blockade alters viability in vivo.
Muscle cells from adult male Schistosoma mansoni have been isolated using a combination of papain digestions and mechanical dissociation procedures. The muscle fibres isolated in this way lacked nuclei but they did contract and relax in response to high [K+], a response which was blocked in the presence of Co2+. From this we conclude that the isolation procedure yields viable muscle fibres useful for physiological studies. Patch-clamp recordings taken from the isolated fibres show a variety of discrete ionic conductances. In inside-out patches one prominent channel was a Ca(2+)-activated K+ channel with a conductance of 195 pS and a selectivity greater than 10:1 for K+ over Na+, Cs+ or NH4+. Percentage open time was dependent on [Ca2+] at the intracellular face. With [Ca2+] at 1 microM or greater percentage open time was greater than 95%; at 0.1 microM it was less than 2%. No voltage sensitivity could be detected in the voltage range from -50 to -10 mV membrane potential. Ba2+ (10 mM), but neither tetraethylammonium nor 3,4-diaminopyridine blocked the channel from the intracellular face. This Ca(2+)-activated K+ channel in the muscle membrane of this acoelomate animal is similar in most respects to the maxi-K+ channels which have been described in a variety of cells from more highly evolved animals.
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Blair et al. (1991) studied Schistosoma mansoni. Intracellular calcium concentration manipulation was evaluated on Channel conductance and percentage open time. In isolated muscle fibres from Schistosoma mansoni, a prominent Ca2+-activated K+ channel was identified with a conductance of 195 pS and >95% open time at ≥1 microM intracellular Ca2+.
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