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Publication : Functional expression of a Kir2.1-like inwardly rectifying potassium channel in mouse mammary secretory cells.

First Author  Kamikawa A Year  2014
Journal  Am J Physiol Cell Physiol Volume  306
Issue  3 Pages  C230-40
PubMed ID  24259419 Mgi Jnum  J:210904
Mgi Id  MGI:5572863 Doi  10.1152/ajpcell.00219.2013
Citation  Kamikawa A, et al. (2014) Functional expression of a Kir2.1-like inwardly rectifying potassium channel in mouse mammary secretory cells. Am J Physiol Cell Physiol 306(3):C230-40
abstractText  K(+) channels in mammary secretory (MS) cells are believed to play a role in transcellular electrolyte transport and thus determining ionic composition of the aqueous phase of milk. However, direct evidence for specific K(+) channel activity in native MS cells is lacking at the single-cell level. Here, we show for the first time that an inwardly rectifying K(+) (Kir) channel is functionally expressed in fully differentiated MS cells that were freshly isolated from the mammary gland of lactating mice. Using the standard whole cell patch-clamp technique, we found that mouse MS cells consistently displayed a K(+) current, whose electrophysiological properties are similar to those previously reported for Kir2.x channels, particularly Kir2.1: 1) current-voltage relationship with strong inward rectification, 2) slope conductance approximately proportional to the square root of external K(+) concentration, 3) voltage- and time-dependent and high-affinity block by external Ba(2+), and 4) voltage-dependent inhibition by external Cs(+). Accordingly, RT-PCR analysis revealed the gene expression of Kir2.1, but not Kir2.2, Kir2.3, and Kir2.4, in lactating mouse mammary gland, and immunohistochemical staining showed Kir2.1 protein expression in the secretory cells. Cell-attached patch recordings from MS cells revealed that a 31-pS K(+) channel with strong inward rectification was likely active at the resting membrane potential. Collectively, the present work demonstrates that a functional Kir2.1-like channel is expressed in lactating mouse MS cells. We propose that the channel might be involved, at least in part, in secretion and/or preservation of ionic components of milk stored into the lumen of these cells.
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