Extracellular glutathione peroxidase (Gpx3) binds specifically to basement membranes of mouse renal cortex tubule cells

被引:121
作者
Olson, Gary E. [2 ]
Whitin, John C. [3 ]
Hill, Kristina E.
Winfrey, Virginia P. [2 ]
Motley, Amy K.
Austin, Lori M.
Deal, Jacqualyn
Cohen, Harvey J. [3 ]
Burk, Raymond F. [1 ]
机构
[1] Vanderbilt Univ, Med Ctr, Div Gastroenterol Hepatol & Nutr, Dept Med,Sch Med, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Sch Med, Dept Cell & Dev Biol, Nashville, TN 37232 USA
[3] Stanford Univ, Dept Pediat, Sch Med, Stanford, CA 94305 USA
关键词
selenoproteins; selenium metabolism; Gpx3 knockout mouse; Gpx3; localization; WHOLE-BODY SELENIUM; SELENOPROTEIN-P; NEUROLOGICAL DYSFUNCTION; HUMAN-PLASMA; MICE; DELETION; KIDNEY; GENE; EXPRESSION; DEFICIENT;
D O I
10.1152/ajprenal.00662.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Olson GE, Whitin JC, Hill KE, Winfrey VP, Motley AK, Austin LM, Deal J, Cohen HJ, Burk RF. Extracellular glutathione peroxidase (Gpx3) binds specifically to basement membranes of mouse renal cortex tubule cells. Am J Physiol Renal Physiol 298: F1244-F1253, 2010. First published December 16, 2009; doi:10.1152/ajprenal.00662.2009.-Glutathione peroxidase-3 (Gpx3), also known as plasma or extracellular glutathione peroxidase, is a selenoprotein secreted primarily by kidney proximal convoluted tubule cells. In this study Gpx3(-/-) mice have been produced and immunocytochemical techniques have been developed to investigate Gpx3 metabolism. Gpx3(-/-) mice maintained the same whole-body content and urinary excretion of selenium as did Gpx3(-/-) mice. They tolerated selenium deficiency without observable ill effects. The simultaneous knockout of Gpx3 and selenoprotein P revealed that these two selenoproteins account for > 97% of plasma selenium. Immunocytochemistry experiments demonstrated that Gpx3 binds selectively, both in vivo and in vitro, to basement membranes of renal cortical proximal and distal convoluted tubules. Based on calculations using selenium content, the kidney pool of Gpx3 is over twice as large as the plasma pool. These data indicate that Gpx3 does not serve in the regulation of selenium metabolism. The specific binding of a large pool of Gpx3 to basement membranes in the kidney cortex strongly suggests a need for glutathione peroxidase activity in the cortical peritubular space.
引用
收藏
页码:F1244 / F1253
页数:10
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