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The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?

Podocytes are considered as the most important cells that determine loss of structure and function of the glomerular filter. We compared the expression of three podocyte markers, i.e.: synaptopodin (SYN), CR1 and neprilysin (NEP) in 107 patients with different forms of glomerulonephritis (GN) and 5...

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Autores principales: Kubiak-Wlekły, Anna, Perkowska-Ptasińska, Agnieszka, Olejniczak, Paweł, Rochowiak, Aleksandra, Kaczmarek, Elżbieta, Durlik, Magdalena, Czekalski, Stanisław, Niemir, Zofia I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Master Publishing Group 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614758/
https://www.ncbi.nlm.nih.gov/pubmed/23675111
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author Kubiak-Wlekły, Anna
Perkowska-Ptasińska, Agnieszka
Olejniczak, Paweł
Rochowiak, Aleksandra
Kaczmarek, Elżbieta
Durlik, Magdalena
Czekalski, Stanisław
Niemir, Zofia I.
author_facet Kubiak-Wlekły, Anna
Perkowska-Ptasińska, Agnieszka
Olejniczak, Paweł
Rochowiak, Aleksandra
Kaczmarek, Elżbieta
Durlik, Magdalena
Czekalski, Stanisław
Niemir, Zofia I.
author_sort Kubiak-Wlekły, Anna
collection PubMed
description Podocytes are considered as the most important cells that determine loss of structure and function of the glomerular filter. We compared the expression of three podocyte markers, i.e.: synaptopodin (SYN), CR1 and neprilysin (NEP) in 107 patients with different forms of glomerulonephritis (GN) and 5 normal kidneys (NK). A quantitative immunohistochemistry was applied to evaluate the expression of podocyte proteins. The results were related with serum creatinine (Scr), estimated glomerular filtration rate (eGFR) and urinary protein. We observed the reduction in the podocyte expression of NEP, SYN and CR1 in proliferative and non-proliferative forms of GN. Interestingly, in mesangial proliferative GN (MesPGN), the expression of SYN and CR1 was lower in IgA-MesPGN than in non-IgA-MesPGN (p<0.005 and p<0.02, respectively). In all the patients, the expression of NEP and SYN was positively related (r=0.53, p=0.02) as that of NEP and CR1 (r=0.39, p=0.04). Yet, clinical correlations with Scr (r=-0.33, p=0.03) and eGFR (r=0.26, p=0.05) were obtained only with respect to CR1. In conclusion, SYN, CR1 and NEP may be used as markers of podocyte loss in patients with GN. However, in agreement with previous studies, the clinical relevance draws a special attention to the expression of CR1.
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spelling pubmed-36147582013-05-01 The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant? Kubiak-Wlekły, Anna Perkowska-Ptasińska, Agnieszka Olejniczak, Paweł Rochowiak, Aleksandra Kaczmarek, Elżbieta Durlik, Magdalena Czekalski, Stanisław Niemir, Zofia I. Int J Biomed Sci Article Podocytes are considered as the most important cells that determine loss of structure and function of the glomerular filter. We compared the expression of three podocyte markers, i.e.: synaptopodin (SYN), CR1 and neprilysin (NEP) in 107 patients with different forms of glomerulonephritis (GN) and 5 normal kidneys (NK). A quantitative immunohistochemistry was applied to evaluate the expression of podocyte proteins. The results were related with serum creatinine (Scr), estimated glomerular filtration rate (eGFR) and urinary protein. We observed the reduction in the podocyte expression of NEP, SYN and CR1 in proliferative and non-proliferative forms of GN. Interestingly, in mesangial proliferative GN (MesPGN), the expression of SYN and CR1 was lower in IgA-MesPGN than in non-IgA-MesPGN (p<0.005 and p<0.02, respectively). In all the patients, the expression of NEP and SYN was positively related (r=0.53, p=0.02) as that of NEP and CR1 (r=0.39, p=0.04). Yet, clinical correlations with Scr (r=-0.33, p=0.03) and eGFR (r=0.26, p=0.05) were obtained only with respect to CR1. In conclusion, SYN, CR1 and NEP may be used as markers of podocyte loss in patients with GN. However, in agreement with previous studies, the clinical relevance draws a special attention to the expression of CR1. Master Publishing Group 2009-03 /pmc/articles/PMC3614758/ /pubmed/23675111 Text en © Anna Kubiak-Wlekly et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Article
Kubiak-Wlekły, Anna
Perkowska-Ptasińska, Agnieszka
Olejniczak, Paweł
Rochowiak, Aleksandra
Kaczmarek, Elżbieta
Durlik, Magdalena
Czekalski, Stanisław
Niemir, Zofia I.
The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title_full The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title_fullStr The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title_full_unstemmed The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title_short The Comparison of the Podocyte Expression of Synaptopodin, CR1 and Neprilysin in Human Glomerulonephritis: Could the Expression of CR1 be Clinically Relevant?
title_sort comparison of the podocyte expression of synaptopodin, cr1 and neprilysin in human glomerulonephritis: could the expression of cr1 be clinically relevant?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614758/
https://www.ncbi.nlm.nih.gov/pubmed/23675111
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