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Conference Paper: Anti-dsDNA antibodies induce epithelial-to-mesenchymal transition and fibrotic processes in human proximal renal tubular epithelial cells
Title | Anti-dsDNA antibodies induce epithelial-to-mesenchymal transition and fibrotic processes in human proximal renal tubular epithelial cells |
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Authors | |
Issue Date | 2012 |
Publisher | American Society of Nephrology. The Journal's web site is located at http://www.jasn.org |
Citation | The 2012 Annual Meeting and Scientific Exposition of the American Society of Nephrology (Kidney Week 2012), San Diego, CA., 30 October-4 November 2012. In Journal of the American Society of Nephrology, 2012, v. 23 abstract suppl., p. 338A, abstract TH-PO1034 How to Cite? |
Abstract | BACKGROUND: Tubulo-interstitial pathology predicts renal prognosis. We investigated the role of anti-dsDNA antibodies in the pathogenesis of tubulo-interstitial pathology in lupus nephritis, focusing on proximal renal tubular epithelial cells (PTEC) and epithelial-to-mesenchymal transition (EMT). METHODS: Female NZBWF1/J mice at different stages of nephritis were sacrificed and kidneys harvested to assess the tubulo-interstitial changes over time. Growth-arrested primary human PTEC were cultured with human polyclonal anti-dsDNA antibodies or control IgG (10μg/ml for both) for periods up to 48h, and investigated for the synthesis of mediators of fibrosis and EMT. RESULTS: NZBWF1/J mice showed progressive tubular damage over time, as denoted by tubular atrophy, protein cast deposition, mononuclear cell infiltration and increasing tubulo-interstitial expression of fibronectin, collagen type I and fibroblast specific protein-1 (FSP-1). Anti-dsDNA antibodies significantly induced the synthesis of soluble and insoluble fibronectin in PTEC after 24h incubation (P<0.01 for both). Anti-dsDNA antibodies induced FSP-1 and β-catenin synthesis (P<0.001 for both), which was accompanied by increased ERK and PKC-α phosphorylation. Inhibition of ERK and PKC-α activation using specific inhibitors reduced anti-dsDNA antibody induced EMT markers and fibronectin synthesis, and preserved normal PTEC phenotype. CONCLUSIONS: Our data demonstrate that anti-dsDNA antibodies contribute to tubulo-interstitial pathology in lupus nephritis via direct effects on PTEC which are mediated through ERK and PKC-α activation. |
Description | Meeting Theme: Curing Kidney Disease Session - Pathobiology: Extracellular Matrix Biology, Fibrosis, Cell Adhesion: abstract TH-PO1034 |
Persistent Identifier | http://hdl.handle.net/10722/186840 |
ISSN | 2023 Impact Factor: 10.3 2023 SCImago Journal Rankings: 3.409 |
DC Field | Value | Language |
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dc.contributor.author | Ho, SSK | en_US |
dc.contributor.author | Yung, S | en_US |
dc.contributor.author | Cheung, KF | en_US |
dc.contributor.author | Tse, WW | en_US |
dc.contributor.author | Chan, DTM | en_US |
dc.date.accessioned | 2013-08-20T12:21:13Z | - |
dc.date.available | 2013-08-20T12:21:13Z | - |
dc.date.issued | 2012 | en_US |
dc.identifier.citation | The 2012 Annual Meeting and Scientific Exposition of the American Society of Nephrology (Kidney Week 2012), San Diego, CA., 30 October-4 November 2012. In Journal of the American Society of Nephrology, 2012, v. 23 abstract suppl., p. 338A, abstract TH-PO1034 | en_US |
dc.identifier.issn | 1046-6673 | - |
dc.identifier.uri | http://hdl.handle.net/10722/186840 | - |
dc.description | Meeting Theme: Curing Kidney Disease | - |
dc.description | Session - Pathobiology: Extracellular Matrix Biology, Fibrosis, Cell Adhesion: abstract TH-PO1034 | - |
dc.description.abstract | BACKGROUND: Tubulo-interstitial pathology predicts renal prognosis. We investigated the role of anti-dsDNA antibodies in the pathogenesis of tubulo-interstitial pathology in lupus nephritis, focusing on proximal renal tubular epithelial cells (PTEC) and epithelial-to-mesenchymal transition (EMT). METHODS: Female NZBWF1/J mice at different stages of nephritis were sacrificed and kidneys harvested to assess the tubulo-interstitial changes over time. Growth-arrested primary human PTEC were cultured with human polyclonal anti-dsDNA antibodies or control IgG (10μg/ml for both) for periods up to 48h, and investigated for the synthesis of mediators of fibrosis and EMT. RESULTS: NZBWF1/J mice showed progressive tubular damage over time, as denoted by tubular atrophy, protein cast deposition, mononuclear cell infiltration and increasing tubulo-interstitial expression of fibronectin, collagen type I and fibroblast specific protein-1 (FSP-1). Anti-dsDNA antibodies significantly induced the synthesis of soluble and insoluble fibronectin in PTEC after 24h incubation (P<0.01 for both). Anti-dsDNA antibodies induced FSP-1 and β-catenin synthesis (P<0.001 for both), which was accompanied by increased ERK and PKC-α phosphorylation. Inhibition of ERK and PKC-α activation using specific inhibitors reduced anti-dsDNA antibody induced EMT markers and fibronectin synthesis, and preserved normal PTEC phenotype. CONCLUSIONS: Our data demonstrate that anti-dsDNA antibodies contribute to tubulo-interstitial pathology in lupus nephritis via direct effects on PTEC which are mediated through ERK and PKC-α activation. | - |
dc.language | eng | en_US |
dc.publisher | American Society of Nephrology. The Journal's web site is located at http://www.jasn.org | - |
dc.relation.ispartof | Journal of the American Society of Nephrology | en_US |
dc.title | Anti-dsDNA antibodies induce epithelial-to-mesenchymal transition and fibrotic processes in human proximal renal tubular epithelial cells | en_US |
dc.type | Conference_Paper | en_US |
dc.identifier.email | Yung, S: ssyyung@hku.hk | en_US |
dc.identifier.email | Cheung, KF: skfc819@hku.hk | en_US |
dc.identifier.email | Tse, WW: kenniskt@hku.hk | en_US |
dc.identifier.email | Chan, DTM: dtmchan@hku.hk | en_US |
dc.identifier.authority | Yung, S=rp00455 | en_US |
dc.identifier.authority | Chan, DTM=rp00394 | en_US |
dc.description.nature | link_to_OA_fulltext | - |
dc.identifier.hkuros | 220417 | en_US |
dc.identifier.volume | 23 | - |
dc.identifier.issue | abstract suppl. | - |
dc.identifier.spage | 338A, abstract TH-PO1034 | en_US |
dc.identifier.epage | 338A, abstract TH-PO1034 | en_US |
dc.publisher.place | United States | - |
dc.identifier.issnl | 1046-6673 | - |