• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to previous page

Characterization of the distribution and localization of IRK channel families in the developing neuronal cells.

Research Project

Project/Area Number 09670060
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General physiology
Research InstitutionKansai Medical University

Principal Investigator

OMORI Koichiro  Kansai Med.Univ., Dept.of Physiol., Assistant Prof., 医学部, 助教授 (80094465)

Co-Investigator(Kenkyū-buntansha) YAMAMOTO Akitsugu  Kansai Med.Univ., Dept.of Physiol., Lecturer, 医学部, 講師 (30174775)
MATSUDA Hiroko  Kansai Med.Univ., Dept.of Physiol., Professor, 医学部, 教授 (10181736)
Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥2,700,000 (Direct Cost: ¥2,700,000)
Fiscal Year 1998: ¥1,000,000 (Direct Cost: ¥1,000,000)
Fiscal Year 1997: ¥1,700,000 (Direct Cost: ¥1,700,000)
KeywordsIRK1 / GIRK1 / central nervous system / COS細胞 / イムノブロット / 内向き整流Kチャネル / パッチクランプ / 遺伝子導入 / バキュロウィルス / Sf9 / PC12
Research Abstract

The inwardly rectifying K^+ channels have been found in a variety of cell types including cardiac myocytes, neuronal cells, skeletal muscle, blood cells, osteoclasts and endothelial cells, and play important roles in maintenance of the resting membrane potential, regulation of the action potential duration and thereby controlling the excitability of the cells.
We examined the localization and distribution of IRK1, one of the classical inwardly rectifying K^+ channel, and GIRK1 that is gated by betagamma subunit of G protein, by using specific antibodies in neuronal cells.
1.The apparent molecular weights of-83 kDa and -65 kDa for the IRK1 and GIRK1, respectively, were detected in mouse cerebral crude membrane fraction, and were larger than the respective expected molecular weight. When these channel proteins were digested with N-glycosidase F, GIRKI shifted to -58 kDa, while IRK1 showed no change, suggesting that IRK1 may have 0-linked oligosaceharide chains.
2.The treatment of the crude membrane fraction with detergents solubilized GIRK1 by -40% of the total contents but hardly extracted IRK1, almost all of which retained in the insoluble fraction. The findings indicate that these channel proteins exist in the cellular organelle in different manner. In the neuronal cells, IRKl may interacts with PSD-95 or PSD-95 like protein which is one of thecytoskeletal protein and resistant to the detergent extraction.
3.We performed the same experiment as described above in cultured rat fetal neurons after cultivation for 4 weeks. Interestingly, -70-80% of both channel proteins were extracted from the cells by the detergent treatment. As neuronal cells in culture can not form mature synaptic junction, both channel proteins could not interact with cytoskeletal proteins correctly, suggesting again the interaction with PSD-95 family protein for IRKI in mature synaptic junction.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (14 results)

All Other

All Publications (14 results)

  • [Publications] Oishi K. et al.: "Neutralization of aspartate residues in the murine inwardly rectifying-." The Journal of Physiology. 510. 675-683 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Fujiseki Y. et al.: "Natriuretic peptide receptors, NPR-A and NPR-B, in cultured rabbit-." The Japanese Journal of Pharmacology. 79 in press. (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Tagawa Y. et al.: "A 60 kDa plasma membrance protein changes its localization to-." Cell Structure and Function. 24 in press. (1999)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Oishi, K et al.: "Neutralization of aspartate residues in the murine inwardly rectifying K^+ channel IRK1 affects the substate behavior in Mg^<2+> block." J.Physiol.510-3. 675-683 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Fujiseki, Y.et al.: "Natriuretc peptide receptors, NPR-A and NPR-B,in cultured rabbit retinal pigment epithelium cells." Jap.J.Pharmacol.79, (in press). (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Tagawa, Y.et al.: "A 60kDa plasma membrane protein changes its localization to autophagosome and autolysosome membrane during induction of autophagy in rat hepatoma cell line, H-4-II-E cells." Cell Struct.Funct.24, (in press). (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] Oishi K.et al.: "Neutralization of aspartate residues in the murine inwardly rectifying K^+-." The Journal of Physiology. 510・3. 675-683 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Omori K.et al.: "Effects of amino-acid substitution in the pore region in IRK1 channel." The Japanese Journal of Physiology. 48 Suppl.S100-S100 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Oishi K.et al.: "Neutralization of the negatively charged residues in the hydrophobic-." The Japanese Journal of Physiology. 48 Suppl.S114-S114 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Fujiseki Y.et al.: "Natriuretic peptide receptors,NPR-A and NPR-B,in cultured rabbit retinal-." The Japanese Journal of Pharmacology. 79(in press). (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] Tagawa Y.et al.: "A 60 kDa plasma membrane protein changes its localization to autophagosome-." Cell Structure and Function. 24(in press). (1999)

    • Related Report
      1998 Annual Research Report
  • [Publications] Omori,K: "Inwardly recifying potassium channels expressed by gene transfection into the Green Monkey Kidney cell line COS-1." The Journal of Physiology. 499・2. 369-378 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Oishi,K: "Effects of magnesium block on site-directed mutagenesis of inwardly rectifying K^+(IRK1) channels." The Japanese Journal of Physiology. 47・Suppl.2. S121-S121 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Yi,X: "Vascular endothelial growth factor expression in choroidal neovascularization in rats." Greafe′s Archive for Clinical and Experimental Ophthalmology. 235・5. 313-319 (1997)

    • Related Report
      1997 Annual Research Report

URL: 

Published: 1997-04-01   Modified: 2016-04-21  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi