TY - JOUR
T1 - Cell-type specific expression of ATP-sensitive potassium channels in the rat hippocampus
AU - Zawar, C.
AU - Plant, T. D.
AU - Schirra, C.
AU - Konnerth, A.
AU - Neumcke, B.
PY - 1999/1/15
Y1 - 1999/1/15
N2 - 1. The distribution of ATP-sensitive K+ channels (K(ATP) channels) was investigated in four cell types in hippocampal slices prepared from 10- to 13-day-old rats: CA1 pyramidal cells, interneurones of stratum radiatum in CA1, complex glial cells of the same area and granule cells of the dentate gyrus. The neuronal cell types were identified visually and characterized by the shapes and patterns of their action potentials and by neurobiotin labelling. 2. The patch-clamp technique was used to study the sensitivity of whole-cell currents to diazoxide (0.3 mM), a K(ATP) channel opener, and to tolbutamide (0.5 mM) or glibenclamide (20 μM), two K(ATP) channel inhibitors. The fraction of cells in which whole-cell currents were activated by diazoxide and inhibited by tolbutamide was 26% of pyramidal cells, 89% of interneurones, 100% of glial cells and 89% of granule cells. The reversal potential of the diazoxide-induced current was at the K+ equilibrium potential and a similar current activated spontaneously when cells were dialysed with an ATP-free pipette solution. 3. Using the single-cell RT-PCR method, the presence of mRNA encoding K(ATP) channel subunits (Kir6.1, Kir6.2, SUR1 and SUR2) was examined in CA1 pyramidal cells and interneurones. Subunit mRNA combinations that can result in functional K(ATP) channels (Kir6.1 together with SUR1, Kir6.2 together with SUR1 or SUR2) were detected in only 17% of the pyramidal cells. On the other hand, K(ATP) channels may be formed in 75% of the interneurones, mainly by the combination of Kir6.2 with SUR1 (58% of all interneurones). The results of these combined analyses indicate that functional K(ATP) channels are present in principal neurones, interneurones and glial cells of the rat hippocampus, but at highly different densities in the four cell types studied.
AB - 1. The distribution of ATP-sensitive K+ channels (K(ATP) channels) was investigated in four cell types in hippocampal slices prepared from 10- to 13-day-old rats: CA1 pyramidal cells, interneurones of stratum radiatum in CA1, complex glial cells of the same area and granule cells of the dentate gyrus. The neuronal cell types were identified visually and characterized by the shapes and patterns of their action potentials and by neurobiotin labelling. 2. The patch-clamp technique was used to study the sensitivity of whole-cell currents to diazoxide (0.3 mM), a K(ATP) channel opener, and to tolbutamide (0.5 mM) or glibenclamide (20 μM), two K(ATP) channel inhibitors. The fraction of cells in which whole-cell currents were activated by diazoxide and inhibited by tolbutamide was 26% of pyramidal cells, 89% of interneurones, 100% of glial cells and 89% of granule cells. The reversal potential of the diazoxide-induced current was at the K+ equilibrium potential and a similar current activated spontaneously when cells were dialysed with an ATP-free pipette solution. 3. Using the single-cell RT-PCR method, the presence of mRNA encoding K(ATP) channel subunits (Kir6.1, Kir6.2, SUR1 and SUR2) was examined in CA1 pyramidal cells and interneurones. Subunit mRNA combinations that can result in functional K(ATP) channels (Kir6.1 together with SUR1, Kir6.2 together with SUR1 or SUR2) were detected in only 17% of the pyramidal cells. On the other hand, K(ATP) channels may be formed in 75% of the interneurones, mainly by the combination of Kir6.2 with SUR1 (58% of all interneurones). The results of these combined analyses indicate that functional K(ATP) channels are present in principal neurones, interneurones and glial cells of the rat hippocampus, but at highly different densities in the four cell types studied.
UR - http://www.scopus.com/inward/record.url?scp=0033556338&partnerID=8YFLogxK
U2 - 10.1111/j.1469-7793.1999.315ae.x
DO - 10.1111/j.1469-7793.1999.315ae.x
M3 - Article
C2 - 9852317
AN - SCOPUS:0033556338
SN - 0022-3751
VL - 514
SP - 327
EP - 341
JO - Journal of Physiology
JF - Journal of Physiology
IS - 2
ER -