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Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression
Renal DNase I is lost in advanced stages of lupus nephritis. Here, we determined if loss of renal DNase I reflects a concurrent loss of urinary DNase I, and whether absence of urinary DNase I predicts disease progression. Mouse and human DNase I protein and DNase I endonuclease activity levels were...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065113/ https://www.ncbi.nlm.nih.gov/pubmed/29624903 http://dx.doi.org/10.1002/cjp2.99 |
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author | Pedersen, Hege L Horvei, Kjersti D Thiyagarajan, Dhivya Norby, Gudrun E Seredkina, Natalya Moroni, Gabriella Eilertsen, Gro Ø Holdaas, Hallvard Strøm, Erik H Bakland, Gunnstein Meroni, Pier‐Luigi Rekvig, Ole P |
author_facet | Pedersen, Hege L Horvei, Kjersti D Thiyagarajan, Dhivya Norby, Gudrun E Seredkina, Natalya Moroni, Gabriella Eilertsen, Gro Ø Holdaas, Hallvard Strøm, Erik H Bakland, Gunnstein Meroni, Pier‐Luigi Rekvig, Ole P |
author_sort | Pedersen, Hege L |
collection | PubMed |
description | Renal DNase I is lost in advanced stages of lupus nephritis. Here, we determined if loss of renal DNase I reflects a concurrent loss of urinary DNase I, and whether absence of urinary DNase I predicts disease progression. Mouse and human DNase I protein and DNase I endonuclease activity levels were determined by western blot, gel, and radial activity assays at different stages of the murine and human forms of the disease. Cellular localization of DNase I was analyzed by immunohistochemistry, immunofluorescence, confocal microscopy, and immunoelectron microscopy. We further compared DNase I levels in human native and transplanted kidneys to determine if the disease depended on autologous renal genes, or whether the nephritic process proceeded also in transplanted kidneys. The data indicate that reduced renal DNase I expression level relates to serious progression of lupus nephritis in murine, human native, and transplanted kidneys. Notably, silencing of renal DNase I correlated with loss of DNase I endonuclease activity in the urine samples. Thus, urinary DNase I levels may therefore be used as a marker of lupus nephritis disease progression and reduce the need for renal biopsies. |
format | Online Article Text |
id | pubmed-6065113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-60651132018-08-02 Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression Pedersen, Hege L Horvei, Kjersti D Thiyagarajan, Dhivya Norby, Gudrun E Seredkina, Natalya Moroni, Gabriella Eilertsen, Gro Ø Holdaas, Hallvard Strøm, Erik H Bakland, Gunnstein Meroni, Pier‐Luigi Rekvig, Ole P J Pathol Clin Res Original Articles Renal DNase I is lost in advanced stages of lupus nephritis. Here, we determined if loss of renal DNase I reflects a concurrent loss of urinary DNase I, and whether absence of urinary DNase I predicts disease progression. Mouse and human DNase I protein and DNase I endonuclease activity levels were determined by western blot, gel, and radial activity assays at different stages of the murine and human forms of the disease. Cellular localization of DNase I was analyzed by immunohistochemistry, immunofluorescence, confocal microscopy, and immunoelectron microscopy. We further compared DNase I levels in human native and transplanted kidneys to determine if the disease depended on autologous renal genes, or whether the nephritic process proceeded also in transplanted kidneys. The data indicate that reduced renal DNase I expression level relates to serious progression of lupus nephritis in murine, human native, and transplanted kidneys. Notably, silencing of renal DNase I correlated with loss of DNase I endonuclease activity in the urine samples. Thus, urinary DNase I levels may therefore be used as a marker of lupus nephritis disease progression and reduce the need for renal biopsies. John Wiley and Sons Inc. 2018-04-06 /pmc/articles/PMC6065113/ /pubmed/29624903 http://dx.doi.org/10.1002/cjp2.99 Text en © 2018 The Authors The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Pedersen, Hege L Horvei, Kjersti D Thiyagarajan, Dhivya Norby, Gudrun E Seredkina, Natalya Moroni, Gabriella Eilertsen, Gro Ø Holdaas, Hallvard Strøm, Erik H Bakland, Gunnstein Meroni, Pier‐Luigi Rekvig, Ole P Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title | Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title_full | Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title_fullStr | Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title_full_unstemmed | Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title_short | Lupus nephritis: low urinary DNase I levels reflect loss of renal DNase I and may be utilized as a biomarker of disease progression |
title_sort | lupus nephritis: low urinary dnase i levels reflect loss of renal dnase i and may be utilized as a biomarker of disease progression |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065113/ https://www.ncbi.nlm.nih.gov/pubmed/29624903 http://dx.doi.org/10.1002/cjp2.99 |
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