POTASSIUM CHANNELS IN RENAL PROXIMAL TUBULE

  • Sanjin D Kovačević Intitut za patološku fiziologiju, Medicinski fakultet Univerziteta u Beogradu
  • Jelena Nešović Ostojić Institut za patološku fiziologiju, Medicinski fakultet, Univerzitet u Beogradu

Sažetak


Potassium channels are a diverse family of membrane proteins and they are present within all cells of the body. They contain two subunits α, which determine the structure of the channel, and β, which can modify the properties of the channel. Those channels are transmembrane proteins that take part in K+ movement across cell membranes via a highly selective pore. The kidneys have crucial role in maintaining total body potassium content, by matching its intake and excretion. In the proximal tubule, K+ absorption is primarily passive and proportional to Na+ and water, so that changes in fluid and potassium transport are closely coupled. Proximal tubular K+ channels are crucial for the maintenance of a hyperpolarized membrane voltage. In leaky epithelia, such as the proximal tubule, the hyperpolarization of the basolateral membrane due to the increase in the K+ conductance of that barrier also results in the hyperpolarization of the apical membrane. They are also involved in regulating cell volume and in recycling potassium across the basolateral membrane. K+ channels of the KCNK and KCNJ gene families have been discovered in the basolateral membrane cell of various species. One of the primary functions of basolateral K+ channels is to recycle K+ across the basolateral membrane for proper function of the Na+-K+ ATPase. Activation by extracellular alkalinization has been associated with a role of TASK-2 in kidney proximal tubule bicarbonate reabsorption. In renal proximal tubules, luminal K+ channels play an important role for restoring the driving force of Na+-coupled transport systems (amino acids, glucose), which depolarize the luminal membrane. Some of these luminal K+ channels are activated directly by the transport-associated depolarization, others are regulated by mediators, second messenger pathways and cell volume.

Key words: proximal tubule, potassium, channels

Biografije autora

Sanjin D Kovačević, Intitut za patološku fiziologiju, Medicinski fakultet Univerziteta u Beogradu
Institut za patološku fiziologiju, saradnik u nastavi
Jelena Nešović Ostojić, Institut za patološku fiziologiju, Medicinski fakultet, Univerzitet u Beogradu
Institut za patološku fiziologiju, vanredni profesor

Reference

Hamilton KL, Devor DC. Basolateral membrane K channels in renal epithelial cells. Am J Physiol Renal Physiol. 2012 May; 302:F1069-1081.

Tian C, Zhu R, Zhu L, Qui T, Cao Z, Kang T. Pottasium channels: structure, diseases and modulators. Chem Biol Drug Des. 2014 Jan; 83:1-26.

Hebert SC, Desir G, Giebisch G, Wang W. Molecular diversity and regulation of renal potassium channels. Physiol Rev. 2005 Jan; 85:319-371.

Palmer BF. Regulation of potassium homeostasis. Clin J Am Soc Nephrol. 2015 Jun; 10(6):1050-1060.

Giebisch G. Renal potassium transport: mechanisms and regulation. Am J Physiol. 1998 May; 274(5 Pt 2):F817-833.

Giebisch G, Krapf R, Wagner C. Renal and extrarenal regulation of potassium. Kidney Int. 2007 Aug; 72:397-410.

Bleich M, Shan QX. Epithelial K+ channels: driving force generation and K+ recycling for epithelial transport with physiological and clinical imlications. Acta Physiologica Sinica 2007 Aug; 59(4):443-453.

Schultz SG, Dubinsky WP. Sodium absorption, volume control and potassium channels: In tribute to a great biologist. J Membrane Biol. 2001 Dec; 184:255-261.

Brochiero E, Wallendorf B, Gagnon D, Laprade R, Lapointe JY. Cloning of rabbit Kir6.1, SUR2A, and SUR2B: possible candidates for a renal KATP channel. Am J Physiol 2002 Feb; 282:F289-F300.

Isomoto S, Kondo C, Kurachi Y. Inwardly rectifying potassium channels: their molecular heterogeneity and function. Jpn J Physiol 1997 Feb; 47:11–39.

Reeves WB, Shah SV. Activation of potassium channels contributes to hypoxic injury in proximal tubules. J Clin Invest 1994 Dec; 94:2289-2294.

Derst C, Hirsch JR, Preisig-Muller R, Wischmeyer E, Karschin A, Doring F, Thomzig A, Veh RW, Schlatter E, Kummer W, Daut J. Cellular localization of the potassium channel Kir7.1 in guinea pig and human kidney. Kidney Int 2001 Jun; 59:2197-2205.

Derst C, Karschin C, Wischmeyer E, Hirsch JR, Preisig-Muller R, Rajan S, Engel H, Grzeschik K, Daut J, Karschin A. Genetic and functional linkage of Kir5.1 and Kir2.1 channel subunits. FEBS Lett 2001 Mar; 491:305-311.

Nakamura K, Hayashi H, Kubokawa M. Proinflamatory cytokines and potassium channels in the kidney. Mediators Inflamm. 2015 Oct; 2015:362768.

Zaika OL, Mamenko M, Palygin O, Boukelmoune N, Staruschenko A, Pochynyuk O. Direct inhibition of basolateral Kir4. 1/5.1 and Kir4. 1 channels in the cortical collecting duct by dopamine. Am J Physiol Renal Physiol. 2013 Nov; 305(9):F1277-87.

Cid LP, Roa Rojas HA, Niemeyer MI, Gonyales W, Araki M, Araki K, Supulveda FV . Task-2: a K2P K(+) channel with complex regulation and diverse physiological functions. Front Physiol. 2013 Jul; 4:198.

Cemerikic D, Nesovic-Ostojic J, Popadic D, Knezevic A, Dragovic S, Milovanovic A, Milovanovic J. Absence of KCNQ1-dependent K+ fluxes in proximal tubular cells of frog kidney. Comp Biochem Physiol A Mol Integr Physiol. 2007 Nov; 48:635-644.

Nesovic-Ostojic J, Markovic-Lipkovski J, Todorovic J, Cirovic S, Kovacevic S, Paunovic A, Cemerikic D, Milovanovic A. Immunolocalization of the TASK2 potassium channel in frog kidney. Folia Biol (Krakow). 2016 Oct; 64(3):183-188.

Enyedi P, Czirjak G. Molecular background of leak K+ currents: two-pore domain potassium channels. Physiol Rev. 2010 Apr; 90(2):559-605.

Warth R. Pottasium channels in epithelial transport. Pflugers Arch. 2003 Aug; 446(5):505-513.

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2017/12/28
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