Section 64
Chapter 63,550

Evidence for an Na+-K+-Cl-cotransporter in mammalian type I vestibular hair cells

Rennie, K.J.; Ashmore, J.F.; Correia, M.J.

American Journal of Physiology. Cell Physiology 273(6): C1972-C1980


ISSN/ISBN: 0363-6143
PMID: 29585101
DOI: 10.1152/ajpcell.1997.273.6.c1972
Accession: 063549290

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In amniotes, there are two types of hair cells, designated I and II, that differ in their morphology, innervation pattern, and ionic membrane properties. Type I cells are unique among hair cells in that their basolateral surfaces are almost completely enclosed by an afferent calyceal nerve terminal. Recently, several lines of evidence have ascribed a motile function to type I hair cells. To investigate this, elevated external K+, which had been used previously to induce hair cell shortening, was used to induce shape changes in dissociated mammalian type I vestibular hair cells. Morphologically identified type I cells shortened and widened when the external K+ concentration was raised isotonically from 2 to 125 mM. The shortening did not require external Ca2+ but was abolished when external Cl- was replaced with gluconate or sulfate and when external Na+ was replaced with N-methyl-d-glucamine. Bumetanide (10-100 μM), a specific blocker of the Na+-K+-Cl- cotransporter, significantly reduced K+-induced shortening. Hyposmotic solution resulted in type I cell shape changes similar to those seen with high K+, i.e., shortening and widening. Type I cells became more spherical in hyposmotic solution, presumably as a result of a volume increase due to water influx. In hypertonic solution, cells became narrower and increased in length. These results suggest that shape changes in type I hair cells induced by high K+ are due, at least in part, to ion and solute entry via an Na+-K+-Cl- cotransporter, which results in cell swelling. A scheme is proposed whereby the type I hair cell depolarizes and K+ leaves the cell via voltage-dependent K+channels and accumulates in the synaptic space between the type I hair cell and calyx. Excess K+ could then be removed from the intercellular space by uptake via the cotransporter.

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