Podocyte Activation of NLRP3 Inflammasomes Contributes to the Development of Proteinuria in Lupus Nephritis
Objective Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte in...
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Published in | Arthritis & rheumatology (Hoboken, N.J.) Vol. 69; no. 8; pp. 1636 - 1646 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Wiley Subscription Services, Inc
01.08.2017
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Subjects | |
Online Access | Get full text |
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Abstract | Objective
Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN.
Methods
A fluorescence‐labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus‐prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry.
Results
NLRP3 inflammasomes were activated in podocytes from lupus‐prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus‐prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species.
Conclusion
NLRP3 inflammasomes were activated in podocytes from lupus‐prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN. |
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AbstractList | Objective Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN. Methods A fluorescence-labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus-prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry. Results NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus-prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species. Conclusion NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN. Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN.OBJECTIVEDevelopment of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN.A fluorescence-labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus-prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry.METHODSA fluorescence-labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus-prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry.NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus-prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species.RESULTSNLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus-prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species.NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN.CONCLUSIONNLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN. Objective Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN. Methods A fluorescence‐labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus‐prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry. Results NLRP3 inflammasomes were activated in podocytes from lupus‐prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus‐prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species. Conclusion NLRP3 inflammasomes were activated in podocytes from lupus‐prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN. Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of LN. The purpose of this study was to investigate whether NLRP3 inflammasome activation is involved in the development of podocyte injury in LN. A fluorescence-labeled caspase 1 inhibitor probe was used to detect the activation of NLRP3 inflammasomes in podocytes derived from lupus-prone NZM2328 mice and from renal biopsy tissues obtained from patients with LN. MCC950, a selective inhibitor of NLRP3, was used to treat NZM2328 mice. Proteinuria, podocyte ultrastructure, and renal pathology were evaluated. In vitro, sera from diseased NZM2328 mice were used to stimulate a podocyte cell line, and the cells were analyzed by flow cytometry. NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from patients with LN. Inhibition of NLRP3 with MCC950 ameliorated proteinuria, renal histologic lesions, and podocyte foot process effacement in lupus-prone mice. In vitro, sera from diseased NZM2328 mice activated NLRP3 inflammasomes in the podocyte cell line through the production of reactive oxygen species. NLRP3 inflammasomes were activated in podocytes from lupus-prone mice and from LN patients. Activation of NLRP3 is involved in the pathogenesis of podocyte injuries and the development of proteinuria in LN. |
Author | Huang, Yuefang Gaskin, Felicia Hu, Haoqiang Fu, Shu Man Guo, Chaohuan Zhao, Jijun Xu, Bihua Yang, Niansheng Zhou, Mianjing Sung, Sun‐sang J. Fu, Rong Chen, Jingxian Wang, Hongyang Jin, Ou Wang, Shuang |
AuthorAffiliation | 1 Department of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China 7 Department of Microbiology, Immunology and Cancer Biology, University of Virginia, Charlottesville, VA 22908-0133, USA 5 Division of Rheumatology and Center of Inflammation, Immunology and Regenerative Medicine, Department of Medicine, University of Virginia, Charlottesville, VA 22908-0133, USA 6 Department of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA 22908-0133, USA 2 Department of Pediatrics, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China 3 Department of Rheumatology, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China 4 Department of Nephrology, Dongguan People’s Hospital, Dongguan, PR China |
AuthorAffiliation_xml | – name: 6 Department of Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA 22908-0133, USA – name: 2 Department of Pediatrics, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China – name: 1 Department of Rheumatology, First Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China – name: 4 Department of Nephrology, Dongguan People’s Hospital, Dongguan, PR China – name: 3 Department of Rheumatology, Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, PR China – name: 7 Department of Microbiology, Immunology and Cancer Biology, University of Virginia, Charlottesville, VA 22908-0133, USA – name: 5 Division of Rheumatology and Center of Inflammation, Immunology and Regenerative Medicine, Department of Medicine, University of Virginia, Charlottesville, VA 22908-0133, USA |
Author_xml | – sequence: 1 givenname: Rong surname: Fu fullname: Fu, Rong organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 2 givenname: Chaohuan surname: Guo fullname: Guo, Chaohuan organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 3 givenname: Shuang surname: Wang fullname: Wang, Shuang organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 4 givenname: Yuefang surname: Huang fullname: Huang, Yuefang organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 5 givenname: Ou surname: Jin fullname: Jin, Ou organization: Third Affiliated Hospital, Sun Yat‐sen University – sequence: 6 givenname: Haoqiang surname: Hu fullname: Hu, Haoqiang organization: Dongguan People's Hospital – sequence: 7 givenname: Jingxian surname: Chen fullname: Chen, Jingxian organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 8 givenname: Bihua surname: Xu fullname: Xu, Bihua organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 9 givenname: Mianjing surname: Zhou fullname: Zhou, Mianjing organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 10 givenname: Jijun surname: Zhao fullname: Zhao, Jijun organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 11 givenname: Sun‐sang J. surname: Sung fullname: Sung, Sun‐sang J. organization: University of Virginia – sequence: 12 givenname: Hongyang surname: Wang fullname: Wang, Hongyang organization: University of Virginia – sequence: 13 givenname: Felicia surname: Gaskin fullname: Gaskin, Felicia organization: University of Virginia – sequence: 14 givenname: Niansheng surname: Yang fullname: Yang, Niansheng email: zsuyns@163.com organization: First Affiliated Hospital, Sun Yat‐sen University – sequence: 15 givenname: Shu Man surname: Fu fullname: Fu, Shu Man organization: University of Virginia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28544564$$D View this record in MEDLINE/PubMed |
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Notes | Supported by the National Natural Science Foundation of China (grants 81471598 and 81671593), the Guangdong Natural Science Foundation (grant 2014A030313096), and the Guangzhou Science and Technology Planning Program (grant 201605122113460). Dr. S. M. Fu's work was supported in part by the NIH (grant R01‐AR‐047988) and the Alliance for Lupus Research (grant TIL332635). Drs. R. Fu, Guo, and S. Wang contributed equally to this work. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to this work. |
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References | 2001; 100 2015; 1 1995; 30 2015; 5 2013; 65 1993; 43 1989; 9 2007; 581 2015; 308 2017; 198 2014; 23 1996; 76 2010; 62 2014; 157 2015; 24 2015; 67 2004; 199 2016; 6 2002; 161 2015; 40 2013; 13 2015; 61 1997; 52 1995; 47 2015; 87 2015; 21 1997; 12 2013; 210 2017 2016 2000; 320 1994; 93 2016; 68 2012; 8 2003; 285 2014; 53 2001; 98 2014; 31 Sun H (e_1_2_6_34_1) 1996; 76 e_1_2_6_32_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_30_1 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_36_1 e_1_2_6_14_1 e_1_2_6_35_1 e_1_2_6_11_1 e_1_2_6_12_1 e_1_2_6_33_1 e_1_2_6_17_1 e_1_2_6_18_1 e_1_2_6_39_1 e_1_2_6_15_1 e_1_2_6_38_1 e_1_2_6_16_1 e_1_2_6_37_1 e_1_2_6_21_1 e_1_2_6_20_1 e_1_2_6_9_1 e_1_2_6_8_1 e_1_2_6_5_1 e_1_2_6_4_1 e_1_2_6_7_1 e_1_2_6_6_1 e_1_2_6_25_1 e_1_2_6_24_1 e_1_2_6_3_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_22_1 e_1_2_6_29_1 e_1_2_6_28_1 e_1_2_6_27_1 e_1_2_6_26_1 28544537 - Arthritis Rheumatol. 2017 Aug;69(8):1517-1520 |
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Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the... Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the pathogenesis of... Objective Development of proteinuria in lupus nephritis (LN) is associated with podocyte dysfunction. The NLRP3 inflammasome has been implicated in the... |
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SubjectTerms | Activation Activation analysis Animals Autoimmune diseases Biopsy Blotting, Western Caspase Caspase 1 - drug effects Caspase 1 - immunology Caspase 1 - metabolism Caspase-1 Cell Line Cytometry Feet Flow Cytometry Fluorescence Heterocyclic Compounds, 4 or More Rings - pharmacology Humans In vitro methods and tests Inflammasomes Inhibitors Interleukin-1beta - drug effects Interleukin-1beta - immunology Interleukin-1beta - metabolism Kidney - drug effects Kidney - immunology Kidney - metabolism Kidney - ultrastructure Kidney Glomerulus - drug effects Kidney Glomerulus - immunology Kidney Glomerulus - metabolism Kidney Glomerulus - ultrastructure Kidneys Lesions Lupus Lupus nephritis Lupus Nephritis - immunology Lupus Nephritis - metabolism Lupus Nephritis - pathology Mice Microscopy, Confocal Microscopy, Electron, Transmission Nephritis NLR Family, Pyrin Domain-Containing 3 Protein - antagonists & inhibitors NLR Family, Pyrin Domain-Containing 3 Protein - immunology Pathogenesis Patients Podocytes - drug effects Podocytes - immunology Podocytes - ultrastructure Proteinuria Proteinuria - immunology Proteinuria - metabolism Proteinuria - pathology Reactive oxygen species Reactive Oxygen Species - metabolism Rodents Sulfones - pharmacology Tissues Ultrastructure |
Title | Podocyte Activation of NLRP3 Inflammasomes Contributes to the Development of Proteinuria in Lupus Nephritis |
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