Acute endotoxemia in mice induces downregulation of megalin and cubilin in the kidney

Schreiber, Andrea and Theilig, Franziska and Schweda, Frank and Hoecherl, Klaus (2012) Acute endotoxemia in mice induces downregulation of megalin and cubilin in the kidney. KIDNEY INTERNATIONAL, 82 (1). pp. 53-59. ISSN 0085-2538,

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Abstract

Severe sepsis is often accompanied by acute renal failure with renal tubular dysfunction. Albuminuria is a common finding in septic patients and we studied whether it was due to an impairment of proximal tubular endocytosis of filtered albumin. We studied the regulation of megalin and cubilin, the two critical multiligand receptors responsible for albumin absorption, during severe experimental endotoxemia. Lipopolysaccharide (LPS) caused a time-and dose-dependent suppression of megalin and cubilin expression that was paralleled by a decrease in plasma albumin levels and an increase in the urine concentration of albumin in mice. Incubation of rat renal cortical slices with LPS also reduced the mRNA expression of megalin and cubilin. Further, LPS suppressed megalin and cubilin mRNA expression in murine primary proximal tubule cells and decreased the uptake of FITC albumin in these cells. In addition, the increase in urine levels of albumin in response to ischemia/reperfusion-induced acute renal failure was paralleled by a decrease in the expression of megalin and cubilin. Thus, our data indicate that the expression of megalin and cubilin is decreased during experimental endotoxemia and in response to renal ischemia/reperfusion injury. This downregulation may contribute, in part, to an increase in urine levels of albumin during acute renal failure. Kidney International (2012) 82, 53-59; doi:10.1038/ki.2012.62; published online 21 March 2012

Item Type: Article
Uncontrolled Keywords: ACUTE-RENAL-FAILURE; ISCHEMIA-REPERFUSION INJURY; SEVERE SEPSIS; SEVERE INFLAMMATION; GLOMERULAR BARRIER; SIZE-SELECTIVITY; PROXIMAL TUBULE; SEPTIC SHOCK; NITRIC-OXIDE; KAPPA-B; acute renal failure; albumin; inflammation; ischemia; lipopolysaccharide
Subjects: 500 Science > 570 Life sciences
Divisions: Biology, Preclinical Medicine > Institut für Physiologie > Prof. Dr. Frank Schweda
Depositing User: Dr. Gernot Deinzer
Date Deposited: 11 May 2020 08:32
Last Modified: 11 May 2020 08:32
URI: https://pred.uni-regensburg.de/id/eprint/18538

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