Ciencias,UNAM

A cAMP regulated K+-selective channel from the sea urchin sperm plasma membrane

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dc.contributor.author Labarca, P
dc.contributor.author Santi, C
dc.contributor.author Zapata, O
dc.contributor.author Morales, E
dc.contributor.author Beltran, C
dc.contributor.author Lievano, A
dc.contributor.author Darszon, A
dc.date.accessioned 2011-01-22T10:28:24Z
dc.date.available 2011-01-22T10:28:24Z
dc.date.issued 1996
dc.identifier.issn 0012-1606
dc.identifier.uri http://hdl.handle.net/11154/2971
dc.description.abstract Ion channels are deeply involved in sperm physiology. In sea urchin sperm cyclic nucleotide levels increase during quimotaxis and in the acrosome reaction (AR). Although cyclic nucleotides are second messengers known to directly or indirectly modulate ion channels, it is not clear how they modulate sperm responses to the egg outer layer. Here, we describe a cAMP regulated Kf-selective channel from sea urchin sperm plasma membranes fused into planar bilayers that may have a role during sea urchin sperm quimotaxis and/or the AR. Its single channel conductance in 100 mM KCl is 103 pS. In bi-ionic experiments, the channel displayed a K+/Na+ permeability ratio (P-K+/P-Na+) of similar to 5. Thus, in sea water its reversal potential would be similar to-13 mV and channel opening would depolarize spermatozoa. The channel has low open probability (P-0 = 0.8 +/- 0.2% at 0 mV applied voltage) and weak voltage dependence. Channel activity is reversibly up-regulated by cAMP in the cis bilayer side, but not by cGMP. This modulation followed a single Langmuir isotherm with an apparent k(d) of 200 mu M At this concentration the channel open probability at 0 mV increased up to 11-fold. TEA(+) blocked the channel only from the trans side. Also Ba2+ in bans blocked the channel in a voltage-dependent manner. (C) 1996 Academic Press, Inc. en_US
dc.language.iso en en_US
dc.title A cAMP regulated K+-selective channel from the sea urchin sperm plasma membrane en_US
dc.type Article en_US
dc.identifier.idprometeo 3114
dc.source.novolpages 174(2):271-280
dc.subject.wos Developmental Biology
dc.description.index WoS: SCI, SSCI o AHCI
dc.relation.journal Developmental Biology

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