Literature DB >> 17548268

Expression of ATP sensitive K+ channel subunit Kir6.1 in rat kidney.

M Zhou1, H J He, R Suzuki, O Tanaka, M Sekiguchi, Y Yasuoka, K Kawahara, H Itoh, H Abe.   

Abstract

ATP-sensitive K+ (K(ATP)) channels in kidney are considered to play roles in regulating membrane potential during the change in intracellular ATP concentration. They are composed of channel subunits (Kir6.1, Kir6.2), which are members of the inwardly rectifying K+ channel family, and sulphonylurea receptors (SUR1, SUR2A and SUR2B), which belong to the ATP-binding cassette superfamily. In the present study, we have investigated the expression and localization of Kir6.1 in rat kidney with Western blot analysis, immunohistochemistry, in situ hybridization histochemistry, and immunoelectron microscopy. Western blot analysis showed that Kir6.1 was expressed in the mitochondria and microsome fractions of rat kidney and very weakly in the membrane fractions. Immunohistochemistry revealed that Kir6.1 was widely distributed in renal tubular epithelial cells, glomerular mesangial cells, and smooth muscles of blood vessels. In immunoelectron microscopy, Kir6.1 is mainly localized in the mitochondria, endoplasmic reticulum (ER), and very weakly in cell membranes. Thus, Kir6.1 is contained in the kidney and may be a candidate of mitochondrial K(ATP) channels.

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Year:  2007        PMID: 17548268

Source DB:  PubMed          Journal:  Eur J Histochem        ISSN: 1121-760X            Impact factor:   3.188


  8 in total

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Journal:  FEBS Lett       Date:  2012-01-21       Impact factor: 4.124

2.  A novel mitochondrial K(ATP) channel assay.

Authors:  Andrew P Wojtovich; David M Williams; Marcin K Karcz; Coeli M B Lopes; Daniel A Gray; Keith W Nehrke; Paul S Brookes
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Authors:  Andrew P Wojtovich; C Owen Smith; Cole M Haynes; Keith W Nehrke; Paul S Brookes
Journal:  Biochim Biophys Acta       Date:  2013-01-02

Review 4.  Basolateral membrane K+ channels in renal epithelial cells.

Authors:  Kirk L Hamilton; Daniel C Devor
Journal:  Am J Physiol Renal Physiol       Date:  2012-02-15

5.  Postconditioning ameliorates mitochondrial DNA damage and deletion after renal ischemic injury.

Authors:  Xiaohua Tan; Lei Zhang; Yunpeng Jiang; Yujia Yang; Wenqi Zhang; Yulin Li; Xiuying Zhang
Journal:  Nephrol Dial Transplant       Date:  2013-09-10       Impact factor: 5.992

6.  Fibroblast growth factor 2 protects against renal ischaemia/reperfusion injury by attenuating mitochondrial damage and proinflammatory signalling.

Authors:  Xiao-Hua Tan; Xiao-Meng Zheng; Li-Xia Yu; Jian He; Hong-Mei Zhu; Xiu-Ping Ge; Xiao-Li Ren; Fa-Qing Ye; Saverio Bellusci; Jian Xiao; Xiao-Kun Li; Jin-San Zhang
Journal:  J Cell Mol Med       Date:  2017-05-24       Impact factor: 5.310

7.  Activation of the AMP-related kinase (AMPK) induces renal vasodilatation and downregulates Nox-derived reactive oxygen species (ROS) generation.

Authors:  Claudia Rodríguez; Cristina Contreras; Javier Sáenz-Medina; Mercedes Muñoz; César Corbacho; Joaquín Carballido; Albino García-Sacristán; Medardo Hernandez; Miguel López; Luis Rivera; Dolores Prieto
Journal:  Redox Biol       Date:  2020-05-16       Impact factor: 11.799

8.  Localization of ATP-sensitive K+ channel subunits in rat liver.

Authors:  Ming Zhou; Kiwamu Yoshikawa; Hideo Akashi; Mitsutaka Miura; Ryoji Suzuki; Tao-Sheng Li; Hiroshi Abe; Yoshio Bando
Journal:  World J Exp Med       Date:  2019-12-19
  8 in total

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