Expression pattern of Kv11 (Ether à-go-go-related gene; erg) K+ channels in the mouse retina.

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Expression pattern of Kv11 (Ether à-go-go-related gene; erg) K+ channels in the mouse retina. / Cordeiro, Sönke; Guseva, Daria; Wulfsen, Iris; Bauer, Christiane K.

In: PLOS ONE, Vol. 6, No. 12, 12, 2011, p. 29490.

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@article{49e094dc4e884023a90890547a339cd3,
title = "Expression pattern of Kv11 (Ether {\`a}-go-go-related gene; erg) K+ channels in the mouse retina.",
abstract = "In response to light, most retinal neurons exhibit gradual changes in membrane potential. Therefore K+ channels that mediate threshold currents are well-suited for the fine-tuning of signal transduction. In the present study we demonstrate the expression of the different Kv11 (ether-{\`a}-go-go related gene; erg) channel subunits in the human and mouse retina by RT PCR and quantitative PCR, respectively. Immunofluorescence analysis with cryosections of mouse retinae revealed the following local distribution of the three Kv11 subunits: Kv11.1 (m-erg1) displayed the most abundant expression with the strongest immunoreactivity in rod bipolar cells. In addition, immunoreactivity was found in the inner part of the outer plexiform layer (OPL), in the inner plexiform layer (IPL) and in the inner segments of photoreceptors. Immunoreactivity for Kv11.2 (m-erg2) was observed in the outer part of the OPL and throughout the IPL. Double-labeling for vGluT1 or synaptophysin indicated a mainly presynaptic localization of Kv11.2. While no significant staining for Kv11.3 (m-erg3) was detected in the neuronal retina, strong Kv11.3 immunoreactivity was present in the apical membrane of the retinal pigment epithelium. The different expression levels were confirmed by real-time PCR showing almost equal levels of Kv11.1 and Kv11.2, while Kv11.3 mRNA expression was significantly lower. The two main splice variants of Kv11.1, isoforms a and b were detected in comparable levels suggesting a possible formation of cGMP/cGK-sensitive Kv11.1 channels in photoreceptors and rod bipolar cells. Taken together, the immunohistological results revealed different expression patterns of the three Kv11 channels in the mouse retina supposing distinct physiological roles.",
keywords = "Animals, Humans, Male, Female, Mice, *Gene Expression Regulation, Ether-A-Go-Go Potassium Channels/*genetics/*metabolism, Protein Subunits/genetics/metabolism, RNA, Messenger/genetics/metabolism, Retina/cytology/*metabolism, Animals, Humans, Male, Female, Mice, *Gene Expression Regulation, Ether-A-Go-Go Potassium Channels/*genetics/*metabolism, Protein Subunits/genetics/metabolism, RNA, Messenger/genetics/metabolism, Retina/cytology/*metabolism",
author = "S{\"o}nke Cordeiro and Daria Guseva and Iris Wulfsen and Bauer, {Christiane K.}",
year = "2011",
doi = "10.1371/journal.pone.0029490",
language = "English",
volume = "6",
pages = "29490",
journal = "PLOS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "12",

}

RIS

TY - JOUR

T1 - Expression pattern of Kv11 (Ether à-go-go-related gene; erg) K+ channels in the mouse retina.

AU - Cordeiro, Sönke

AU - Guseva, Daria

AU - Wulfsen, Iris

AU - Bauer, Christiane K.

PY - 2011

Y1 - 2011

N2 - In response to light, most retinal neurons exhibit gradual changes in membrane potential. Therefore K+ channels that mediate threshold currents are well-suited for the fine-tuning of signal transduction. In the present study we demonstrate the expression of the different Kv11 (ether-à-go-go related gene; erg) channel subunits in the human and mouse retina by RT PCR and quantitative PCR, respectively. Immunofluorescence analysis with cryosections of mouse retinae revealed the following local distribution of the three Kv11 subunits: Kv11.1 (m-erg1) displayed the most abundant expression with the strongest immunoreactivity in rod bipolar cells. In addition, immunoreactivity was found in the inner part of the outer plexiform layer (OPL), in the inner plexiform layer (IPL) and in the inner segments of photoreceptors. Immunoreactivity for Kv11.2 (m-erg2) was observed in the outer part of the OPL and throughout the IPL. Double-labeling for vGluT1 or synaptophysin indicated a mainly presynaptic localization of Kv11.2. While no significant staining for Kv11.3 (m-erg3) was detected in the neuronal retina, strong Kv11.3 immunoreactivity was present in the apical membrane of the retinal pigment epithelium. The different expression levels were confirmed by real-time PCR showing almost equal levels of Kv11.1 and Kv11.2, while Kv11.3 mRNA expression was significantly lower. The two main splice variants of Kv11.1, isoforms a and b were detected in comparable levels suggesting a possible formation of cGMP/cGK-sensitive Kv11.1 channels in photoreceptors and rod bipolar cells. Taken together, the immunohistological results revealed different expression patterns of the three Kv11 channels in the mouse retina supposing distinct physiological roles.

AB - In response to light, most retinal neurons exhibit gradual changes in membrane potential. Therefore K+ channels that mediate threshold currents are well-suited for the fine-tuning of signal transduction. In the present study we demonstrate the expression of the different Kv11 (ether-à-go-go related gene; erg) channel subunits in the human and mouse retina by RT PCR and quantitative PCR, respectively. Immunofluorescence analysis with cryosections of mouse retinae revealed the following local distribution of the three Kv11 subunits: Kv11.1 (m-erg1) displayed the most abundant expression with the strongest immunoreactivity in rod bipolar cells. In addition, immunoreactivity was found in the inner part of the outer plexiform layer (OPL), in the inner plexiform layer (IPL) and in the inner segments of photoreceptors. Immunoreactivity for Kv11.2 (m-erg2) was observed in the outer part of the OPL and throughout the IPL. Double-labeling for vGluT1 or synaptophysin indicated a mainly presynaptic localization of Kv11.2. While no significant staining for Kv11.3 (m-erg3) was detected in the neuronal retina, strong Kv11.3 immunoreactivity was present in the apical membrane of the retinal pigment epithelium. The different expression levels were confirmed by real-time PCR showing almost equal levels of Kv11.1 and Kv11.2, while Kv11.3 mRNA expression was significantly lower. The two main splice variants of Kv11.1, isoforms a and b were detected in comparable levels suggesting a possible formation of cGMP/cGK-sensitive Kv11.1 channels in photoreceptors and rod bipolar cells. Taken together, the immunohistological results revealed different expression patterns of the three Kv11 channels in the mouse retina supposing distinct physiological roles.

KW - Animals

KW - Humans

KW - Male

KW - Female

KW - Mice

KW - Gene Expression Regulation

KW - Ether-A-Go-Go Potassium Channels/genetics/metabolism

KW - Protein Subunits/genetics/metabolism

KW - RNA, Messenger/genetics/metabolism

KW - Retina/cytology/metabolism

KW - Animals

KW - Humans

KW - Male

KW - Female

KW - Mice

KW - Gene Expression Regulation

KW - Ether-A-Go-Go Potassium Channels/genetics/metabolism

KW - Protein Subunits/genetics/metabolism

KW - RNA, Messenger/genetics/metabolism

KW - Retina/cytology/metabolism

U2 - 10.1371/journal.pone.0029490

DO - 10.1371/journal.pone.0029490

M3 - SCORING: Journal article

VL - 6

SP - 29490

JO - PLOS ONE

JF - PLOS ONE

SN - 1932-6203

IS - 12

M1 - 12

ER -