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1 Institute of Neuroscience, University of Oregon, Eugene, Oregon, United States
2 Howard Hughes Medical Institute, Columbia University Medical Center, New York, New York, United States
* To whom correspondence should be addressed. E-mail: shawn{at}lox.uoregon.edu.
Post-embryonic developmental changes in electrophysiological properties of the AIY interneuron class were investigated using whole-cell voltage-clamp. AIY interneurons displayed an increase in cell capacitance during larval development, whereas steady-state current amplitude did not increase. The time course of the outward membrane current, carried at least in part by K+ ions, matured, from a slowly activating, sustained current to a rapidly-activating, decaying current. We also investigated how the development of capacitance and outward current was altered by loss-of-function mutations in genes expressed in AIY. One such gene, the LIM homeobox gene ttx-3, is known to be involved in the specification of the AIY neuronal subtype. In ttx-3 mutants, capacitance and outward current matured precociously. In mutants of the gene wrk-1, an immunoglobulin superfamily (IgSF) member whose expression is regulated by ttx-3, capacitance matured normally, whereas outward current matured precociously. We conclude that AIY interneurons contain distinct pathways for regulating capacitance and membrane current.
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