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Collagen IVα345 dysfunction in glomerular basement membrane diseases. I. Discovery of a COL4A3 variant in familial Goodpasture's and Alport diseases.
Pokidysheva, Elena N; Seeger, Harald; Pedchenko, Vadim; Chetyrkin, Sergei; Bergmann, Carsten; Abrahamson, Dale; Cui, Zhao Wei; Delpire, Eric; Fervenza, Fernando C; Fidler, Aaron L; Fogo, Agnes B; Gaspert, Ariana; Grohmann, Maik; Gross, Oliver; Haddad, George; Harris, Raymond C; Kashtan, Clifford; Kitching, A Richard; Lorenzen, Johan M; McAdoo, Stephen; Pusey, Charles D; Segelmark, Marten; Simmons, Alicia; Voziyan, Paul A; Wagner, Timo; Wüthrich, Rudolf P; Zhao, Ming-Hui; Boudko, Sergei P; Kistler, Andreas D; Hudson, Billy G.
Afiliação
  • Pokidysheva EN; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Seeger H; Nephrology Division, University Hospital Zurich, Zurich, Switzerland.
  • Pedchenko V; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Chetyrkin S; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Bergmann C; Department of Medicine and Nephrology, University Hospital Freiburg, Freiburg, Germany; Medizinische Genetik Mainz, Limbach Genetics, Mainz, Germany.
  • Abrahamson D; Department of Anatomy and Cell Biology, University of Kansas Medical Center, Kansas City, Kansas, USA.
  • Cui ZW; Renal Division, Peking University First Hospital, Beijing, PR China.
  • Delpire E; Department of Anesthesiology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA.
  • Fervenza FC; Division of Nephrology and Hypertension, Mayo Clinic, Rochester, Minnesota, USA.
  • Fidler AL; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Aspirnaut Program, Vanderbilt University Medical Center, Nashville, Tennessee,
  • Fogo AB; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Gaspert A; Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
  • Grohmann M; Medizinische Genetik Mainz, Limbach Genetics, Mainz, Germany.
  • Gross O; Clinic of Nephrology and Rheumatology, University Medical Center Goettingen, University of Goettingen, Goettingen, Germany.
  • Haddad G; Nephrology Division, University Hospital Zurich, Zurich, Switzerland.
  • Harris RC; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Kashtan C; Division of Pediatric Nephrology, University of Minnesota Medical School and Masonic Children's Hospital, Minneapolis, Minnesota, USA.
  • Kitching AR; Centre for Inflammatory Diseases, Monash University Department Medicine, Nephrology, Monash Health, Clayton, VIC, Australia.
  • Lorenzen JM; Nephrology Division, University Hospital Zurich, Zurich, Switzerland.
  • McAdoo S; Centre for Inflammatory Disease, Imperial College London, London, UK.
  • Pusey CD; Centre for Inflammatory Disease, Imperial College London, London, UK.
  • Segelmark M; Department of Biochemistry, Vanderbilt University, Nashville, Tennessee, USA.
  • Simmons A; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Aspirnaut Program, Vanderbilt University Medical Center, Nashville, Tennessee,
  • Voziyan PA; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
  • Wagner T; Medizinische Genetik Mainz, Limbach Genetics, Mainz, Germany.
  • Wüthrich RP; Nephrology Division, University Hospital Zurich, Zurich, Switzerland.
  • Zhao MH; Renal Division, Peking University First Hospital, Beijing, PR China.
  • Boudko SP; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Department of Biochemistry, Vanderbilt University, Nashville, Tennessee, USA.
  • Kistler AD; Department of Internal Medicine, Kantonsspital Frauenfeld, Frauenfeld, Switzerland.
  • Hudson BG; Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Center for Matrix Biology, Vanderbilt University Medical Center, Nashville, Tennessee, USA; Aspirnaut Program, Vanderbilt University Medical Center, Nashville, Tennessee,
J Biol Chem ; 296: 100590, 2021.
Article em En | MEDLINE | ID: mdl-33774048
Diseases of the glomerular basement membrane (GBM), such as Goodpasture's disease (GP) and Alport syndrome (AS), are a major cause of chronic kidney failure and an unmet medical need. Collagen IVα345 is an important architectural element of the GBM that was discovered in previous research on GP and AS. How this collagen enables GBM to function as a permselective filter and how structural defects cause renal failure remain an enigma. We found a distinctive genetic variant of collagen IVα345 in both a familial GP case and four AS kindreds that provided insights into these mechanisms. The variant is an 8-residue appendage at the C-terminus of the α3 subunit of the α345 hexamer. A knock-in mouse harboring the variant displayed GBM abnormalities and proteinuria. This pathology phenocopied AS, which pinpointed the α345 hexamer as a focal point in GBM function and dysfunction. Crystallography and assembly studies revealed underlying hexamer mechanisms, as described in Boudko et al. and Pedchenko et al. Bioactive sites on the hexamer surface were identified where pathogenic pathways of GP and AS converge and, potentially, that of diabetic nephropathy (DN). We conclude that the hexamer functions include signaling and organizing macromolecular complexes, which enable GBM assembly and function. Therapeutic modulation or replacement of α345 hexamer could therefore be a potential treatment for GBM diseases, and this knock-in mouse model is suitable for developing gene therapies.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença Antimembrana Basal Glomerular / Colágeno Tipo IV / Mutação / Nefrite Hereditária Limite: Animals Idioma: En Revista: J Biol Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doença Antimembrana Basal Glomerular / Colágeno Tipo IV / Mutação / Nefrite Hereditária Limite: Animals Idioma: En Revista: J Biol Chem Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos