Mocker, Alexander;
Hilgers, Karl F.;
Cordasic, Nada;
Wachtveitl, Rainer;
Menendez-Castro, Carlos;
Woelfle, Joachim;
Hartner, Andrea;
Fahlbusch, Fabian B.
Renal Chemerin Expression is Induced in Models of Hypertensive Nephropathy and Glomerulonephritis and Correlates with Markers of Inflammation and Fibrosis
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Media type:
E-Article
Title:
Renal Chemerin Expression is Induced in Models of Hypertensive Nephropathy and Glomerulonephritis and Correlates with Markers of Inflammation and Fibrosis
Contributor:
Mocker, Alexander;
Hilgers, Karl F.;
Cordasic, Nada;
Wachtveitl, Rainer;
Menendez-Castro, Carlos;
Woelfle, Joachim;
Hartner, Andrea;
Fahlbusch, Fabian B.
Published:
MDPI AG, 2019
Published in:
International Journal of Molecular Sciences, 20 (2019) 24, Seite 6240
Language:
English
DOI:
10.3390/ijms20246240
ISSN:
1422-0067
Origination:
Footnote:
Description:
Chemerin and its receptor, chemokine-like receptor 1 (CmklR1), are associated with chemotaxis, inflammation, and endothelial function, especially in metabolic syndrome, coronary heart disease, and hypertension. In humans, circulating chemerin levels and renal function show an inverse relation. So far, little is known about the potential role of chemerin in hypertensive nephropathy and renal inflammation. Therefore, we determined systemic and renal chemerin levels in 2-kidney-1-clip (2k1c) hypertensive and Thy1.1 nephritic rats, respectively, to explore the correlation between chemerin and markers of renal inflammation and fibrosis. Immunohistochemistry revealed a model-specific induction of chemerin expression at the corresponding site of renal damage (tubular vs. glomerular). In both models, renal expression of chemerin (RT-PCR, Western blot) was increased and correlated positively with markers of inflammation and fibrosis. In contrast, circulating chemerin levels remained unchanged. Taken together, these findings demonstrate that renal chemerin expression is associated with processes of inflammation and fibrosis-related to renal damage. However, its use as circulating biomarker of renal inflammation seems to be limited in our rat models.