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Glomerular type 1 angiotensin receptors augment kidney injury and inflammation in murine autoimmune nephritis

Crowley, S. D. (author)
Vasievich, M. P. (author)
Ruiz, P. (author)
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Gould, S. K. (author)
Parsons, K. K. (author)
Pazmino, A. K. (author)
Facemire, C. (author)
Chen, B. J. (author)
Kim, H. S. (author)
Tran, T. T. (author)
Pisetsky, D. S. (author)
Barisoni, L. (author)
Prieto-Carrasquero, M. C. (author)
Jeansson, Marie, 1971 (author)
Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine,Lunenfeld-Tanenbaum Research Institute, Mount Sinai Hospital
Foster, M. H. (author)
Coffman, T. M. (author)
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 (creator_code:org_t)
2009
2009
English.
In: J Clin Invest. - 1558-8238 .- 1558-8238 .- 0021-9738. ; 119:4, s. 943-53
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Studies in humans and animal models indicate a key contribution of angiotensin II to the pathogenesis of glomerular diseases. To examine the role of type 1 angiotensin (AT1) receptors in glomerular inflammation associated with autoimmune disease, we generated MRL-Faslpr/lpr (lpr) mice lacking the major murine type 1 angiotensin receptor (AT1A); lpr mice develop a generalized autoimmune disease with glomerulonephritis that resembles SLE. Surprisingly, AT1A deficiency was not protective against disease but instead substantially accelerated mortality, proteinuria, and kidney pathology. Increased disease severity was not a direct effect of immune cells, since transplantation of AT1A-deficient bone marrow did not affect survival. Moreover, autoimmune injury in extrarenal tissues, including skin, heart, and joints, was unaffected by AT1A deficiency. In murine systems, there is a second type 1 angiotensin receptor isoform, AT1B, and its expression is especially prominent in the renal glomerulus within podocytes. Further, expression of renin was enhanced in kidneys of AT1A-deficient lpr mice, and they showed evidence of exaggerated AT1B receptor activation, including substantially increased podocyte injury and expression of inflammatory mediators. Administration of losartan, which blocks all type 1 angiotensin receptors, reduced markers of kidney disease, including proteinuria, glomerular pathology, and cytokine mRNA expression. Since AT1A-deficient lpr mice had low blood pressure, these findings suggest that activation of type 1 angiotensin receptors in the glomerulus is sufficient to accelerate renal injury and inflammation in the absence of hypertension.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)

Keyword

Animals
Autoimmune Diseases/*etiology/immunology/pathology/physiopathology
Chemokines/genetics
Cytokines/genetics
Female
Kidney/injuries/pathology/physiopathology
Male
Mice
Mice
Inbred MRL lpr
Mice
Knockout
Nephritis/*etiology/immunology/pathology/physiopathology
RNA
Messenger/genetics/metabolism
Receptor
Angiotensin
Type 1/deficiency/genetics/*physiology
Renin-Angiotensin System/physiology

Publication and Content Type

ref (subject category)
art (subject category)

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