Netrin G1 Is a Novel Target Antigen in Primary Membranous Nephropathy

Background: Primary membranous nephropathy (MN) is caused by circulating autoantibodies (ab) binding to antigens on the podocyte surface. PLA2R1 is the main target antigen in 70-80% of cases, but the pathogenesis is unresolved in 10-15% of patients. Methods: We used native Western blotting to identify IgG4-ab in the serum of the index MN patient, which binds an antigen endogenously expressed on podocyte membranes. These IgG4-ab were used to immunoprecipitate the target antigen and mass spectrometry used to identify Netrin G1 (NTNG1). Native Western blot and ELISA analyzed NTNG1-ab in cohorts of 888 patients with MN or other glomerular diseases. Results: NTNG1 was identified as a novel target antigen in MN. It is a membrane protein expressed in healthy podocytes. Immunohistochemistry confirmed granular NTNG1 in subepithelial glomerular immune deposits. In prospective and retrospective MN cohorts, we identified three patients with NTNG1-associated MN, who showed IgG4-dominant circulating NTNG1-ab, enhanced NTNG1 expression in the kidney, and glomerular IgG4 deposits. No NTNG1-ab were identified in 561 PLA2R1-ab positive patients, 27 THSD7A-ab positive patients, and 77 patients with other glomerular diseases. In two patients with available followup of 2 and 4 years, both NTNG1-ab and proteinuria persisted. Conclusions: NTNG1 expands the repertoire of target antigens in patients with MN. The clinical role of NTNG1-ab remains to be defined.

[1]  M. Haas,et al.  Hematopoietic Stem Cell Transplant-Membranous Nephropathy Is Associated with Protocadherin FAT1 , 2022, Journal of the American Society of Nephrology : JASN.

[2]  A. Brazma,et al.  The PRIDE database resources in 2022: a hub for mass spectrometry-based proteomics evidences , 2021, Nucleic Acids Res..

[3]  M. Granato,et al.  Robo2 Drives Target-Selective Peripheral Nerve Regeneration in Response to Glia-Derived Signals , 2020, The Journal of Neuroscience.

[4]  N. Bec,et al.  Contactin-1 is a novel target antigen in membranous nephropathy associated with chronic inflammatory demyelinating polyneuropathy. , 2021, Kidney international.

[5]  J. Duffield,et al.  The glomerular filtration barrier: a structural target for novel kidney therapies , 2021, Nature Reviews Drug Discovery.

[6]  Aaron J. Storey,et al.  Transforming Growth Factor Beta Receptor 3 (TGFBR3)–Associated Membranous Nephropathy , 2021, Kidney360.

[7]  Aaron J. Storey,et al.  Serine Protease HTRA1 as a Novel Target Antigen in Primary Membranous Nephropathy , 2021, Journal of the American Society of Nephrology : JASN.

[8]  Sidhartha Chaudhry,et al.  Protocadherin 7–Associated Membranous Nephropathy , 2020, Journal of the American Society of Nephrology : JASN.

[9]  Aaron J. Storey,et al.  Neural cell adhesion molecule 1 is a novel autoantigen in membranous lupus nephritis. , 2020, Kidney international.

[10]  F. Emma,et al.  Semaphorin 3B-associated membranous nephropathy is a distinct type of disease predominantly present in pediatric patients. , 2020, Kidney international.

[11]  W. Dębek,et al.  Ubiquitin carboxy‐terminal hydrolase L1 – physiology and pathology , 2020, Cell Biochemistry and Function.

[12]  M. Jadoul,et al.  Neural epidermal growth factor-like 1 protein (NELL-1) associated membranous nephropathy. , 2020, Kidney international.

[13]  G. Zahner,et al.  Clinical Relevance of Domain-Specific Phospholipase A2 Receptor 1 Antibody Levels in Patients with Membranous Nephropathy. , 2019, Journal of the American Society of Nephrology : JASN.

[14]  Seung-Hee Lee,et al.  NGL-1/LRRC4C-Mutant Mice Display Hyperactivity and Anxiolytic-Like Behavior Associated With Widespread Suppression of Neuronal Activity , 2019, Frontiers in Molecular Neuroscience.

[15]  R. Stahl,et al.  Role of phospholipase A2 receptor 1 antibody level at diagnosis for long-term renal outcome in membranous nephropathy , 2019, PloS one.

[16]  Y. Bae,et al.  NGL-1/LRRC4C Deletion Moderately Suppresses Hippocampal Excitatory Synapse Development and Function in an Input-Independent Manner , 2019, Front. Mol. Neurosci..

[17]  U. Specks,et al.  Exostosin 1/Exostosin 2-Associated Membranous Nephropathy. , 2019, Journal of the American Society of Nephrology : JASN.

[18]  R. Stahl,et al.  Diagnostic role of renal biopsy in PLA2R1-antibody-positive patients with nephrotic syndrome , 2019, Modern Pathology.

[19]  R. Stahl,et al.  Antigen-Specific IgG Subclasses in Primary and Malignancy-Associated Membranous Nephropathy , 2018, Front. Immunol..

[20]  R. Stahl,et al.  Characterization of autoantibodies in primary membranous nephropathy and their clinical significance , 2018, Expert review of clinical immunology.

[21]  Christopher S. Hughes,et al.  Single-pot, solid-phase-enhanced sample preparation for proteomics experiments , 2018, Nature Protocols.

[22]  Belinda Jim,et al.  Proteinuric Kidney Diseases: A Podocyte's Slit Diaphragm and Cytoskeleton Approach , 2018, Front. Med..

[23]  D. Salant,et al.  An Indirect Immunofluorescence Method Facilitates Detection of Thrombospondin Type 1 Domain-Containing 7A-Specific Antibodies in Membranous Nephropathy. , 2017, Journal of the American Society of Nephrology : JASN.

[24]  Martin Eisenacher,et al.  PRIDE Inspector Toolsuite: Moving Toward a Universal Visualization Tool for Proteomics Data Standard Formats and Quality Assessment of ProteomeXchange Datasets , 2015, Molecular & Cellular Proteomics.

[25]  G. Drewes,et al.  Thermal proteome profiling for unbiased identification of direct and indirect drug targets using multiplexed quantitative mass spectrometry , 2015, Nature Protocols.

[26]  Markus Gödel,et al.  Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy. , 2015, The New England journal of medicine.

[27]  J. Klein,et al.  Thrombospondin type-1 domain-containing 7A in idiopathic membranous nephropathy. , 2015, The New England journal of medicine.

[28]  Jeroen Krijgsveld,et al.  Ultrasensitive proteome analysis using paramagnetic bead technology , 2014, Molecular systems biology.

[29]  J. Wetzels,et al.  Development of a standardized ELISA for the determination of autoantibodies against human M-type phospholipase A2 receptor in primary membranous nephropathy. , 2013, Clinica chimica acta; international journal of clinical chemistry.

[30]  E. Jones,et al.  Structural basis for cell surface patterning through NetrinG–NGL interactions , 2011, The EMBO journal.

[31]  S. Balabanov,et al.  Ubiquitin C-terminal hydrolase-l1 activity induces polyubiquitin accumulation in podocytes and increases proteinuria in rat membranous nephropathy. , 2011, The American journal of pathology.

[32]  G. Remuzzi,et al.  Early-childhood membranous nephropathy due to cationic bovine serum albumin. , 2011, The New England journal of medicine.

[33]  克治 桑門 海外論文紹介 : M-Type Phospholipase A2 Receptor as Target Antigen in Idiopathic Membranous Nephropathy , 2010 .

[34]  M. Segal,et al.  The Spine Apparatus, Synaptopodin, and Dendritic Spine Plasticity , 2010, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[35]  D. Hochstrasser,et al.  Relative quantification of proteins in human cerebrospinal fluids by MS/MS using 6-plex isobaric tags. , 2008, Analytical chemistry.

[36]  A. Afenjar,et al.  Netrin G1 mutations are an uncommon cause of atypical Rett syndrome with or without epilepsy. , 2007, Pediatric neurology.

[37]  Shigeyoshi Itohara,et al.  Axonal netrin-Gs transneuronally determine lamina-specific subdendritic segments , 2007, Neuroscience Research.

[38]  R. Weinberg,et al.  NGL family PSD-95–interacting adhesion molecules regulate excitatory synapse formation , 2006, Nature Neuroscience.

[39]  A. Clarke,et al.  NTNG1 mutations are a rare cause of Rett syndrome , 2006, American journal of medical genetics. Part A.

[40]  H. Schägger,et al.  Blue native PAGE , 2006, Nature Protocols.

[41]  S. Itohara,et al.  Human netrin-G1 isoforms show evidence of differential expression. , 2005, Genomics.

[42]  Shigeyoshi Itohara,et al.  A family-based association study and gene expression analyses of netrin-G1 and -G2 genes in schizophrenia , 2005, Biological Psychiatry.

[43]  A. Gurney,et al.  The netrin-G1 ligand NGL-1 promotes the outgrowth of thalamocortical axons , 2003, Nature Neuroscience.

[44]  J. Haymann,et al.  Antenatal membranous glomerulonephritis due to anti-neutral endopeptidase antibodies. , 2002, The New England journal of medicine.

[45]  S. Itohara,et al.  Netrin-G1: a Novel Glycosyl Phosphatidylinositol-Linked Mammalian Netrin That Is Functionally Divergent from Classical Netrins , 2000, The Journal of Neuroscience.