Functional analysis of purinergic receptors using IMCT technology in transgenic mouse retina
| Project/Area Number |
16500268
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Neurophysiology and muscle physiology
|
|---|
| Research Institution | Keio University |
|---|
Principal Investigator |
KANEDA Makoto Keio University, Assistant Professor, 医学部, 助教授 (30214480)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
KANEKO Akimichi Seijo University, Professor, リハビリテーション学部, 教授 (00051491)
|
|---|
| Project Period (FY) |
2004 – 2005
|
| Project Status |
Completed (Fiscal Year 2005)
|
| Budget Amount *help |
¥3,200,000 (Direct Cost: ¥3,200,000)
Fiscal Year 2005: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 2004: ¥2,400,000 (Direct Cost: ¥2,400,000)
|
|---|
| Keywords | retina / ATP / purinergic receptors / マウス |
|---|
| Research Abstract |
We investigated the distribution of P2X-purinoceptor families in the cholinergic amacrine cells of the mouse retina by the immunohistochemical technique and the patch clamp technique. The immunoreactivity for P2X2-purinoceptors selectively distributed in the OFF-type cholinergic amacrine cells but not in the ON-type cholinergic amacrine cells. The immunoreactivity for P2X2-purinoceptors in the OFF-type cholinergic amacrine cells disappeared when IMCT technology was introduced to ablate the cholinergic amacrine cells selectively from the retinal circuit. These immunohistochemical studies indicate that P2X2-purinoceptors are selectively expressed on the OFF-type cholinergic amacrine cells. In the slice preparation of the transgenic mouse retina, the cholinergic amacrine cells were identified by the signals of green fluorescent protein. Under the patch clamp recordings, responses to ATP in the OFF-type cholinergic amacrine cells were greater than those in the ON-type cholinergic amacrine cells. No responses to ATP were observed in the non-cholinergic amacrine cells. The responses of ATP in the OFF-type cholinergic amacrine cells were mediated by the P2X2-purinoceptors. The electrophysiological data also support that P2X2-purinoceptors are selectively expressed in the OFF-type cholinergic amacrine cells. ATP also increased the GABAergic inputs to the dendrites of both the ON-type and the OFF-type cholinergic amacrine cells. The increase in the GABAergic inputs were mediated by the different types of P2X-purinoceptors.
|
Report
(3 results)
Research Products
(17 results)
-
-
-
-
-
-
-
-
[Journal Article] OFF-cholinergic-pathway-selective localization of P2X2-purinoceptors in the mouse retina.2004
Author(s)
Kaneda, M., Ishii, K., Morishima, Y., Akagi, T., Yamazaki, Y., Nakanishi, S., Hashikawa, T.
-
Journal Title
J. Comp. Neurol. 476
Pages: 103-111
Description
「研究成果報告書概要(和文)」より
Related Report
-
[Journal Article] A nonsense mutation of the sodium channel gene SCN2A in apatient with intractable epilepsy and mental decline.2004
Author(s)
Kamiya, K., Kaneda, M., Sugawara, T., Mazaki, E., Okamura, N., Montal, M., Makita, N, Tanaka, M., Fukushima, K., Fujiwara, T., Inoue, Y., Yamakawa, K.
-
Journal Title
J. Neurosci. 24
Pages: 2690-2698
Description
「研究成果報告書概要(和文)」より
Related Report
-
-
[Journal Article] OFF-cholinergic-pathway-selective localization of P2X2-purinoceptors in the mouse retina.2004
Author(s)
Kaneda, M., Ishii, K., Morishima, Y.Akagi, T, Yamazaki, Y., Nakanishi, S., Hashikawa, T.
-
Journal Title
J.Comp.Neurol. 476
Pages: 103-111
Description
「研究成果報告書概要(欧文)」より
Related Report
-
[Journal Article] A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline.2004
Author(s)
Kamiya, K., Kaneda, M., Sugawara, T., Mazaki, E., Okamura, N., Montal, M., Makita, N, Tanaka, M., Fukushima, K., Fujiwara, T., Inoue, Y., Yamakawa, K.
-
Journal Title
J.Neurosci. 24
Pages: 2690-2698
Description
「研究成果報告書概要(欧文)」より
Related Report
-
[Journal Article] OFF-cholinergic-pathway-selective localization of P2X2-purinoceptors in the mouse retina.2004
Author(s)
Kaneda, M., Ishii, K., Morishima, Y., Akagi, T., Yamazaki, Y., Nakanishi, S., Hashikawa T.
-
Journal Title
J.Comp.Neurol. 476
Pages: 103-111
Related Report
-
-
-
-
