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Mutations in KIRREL1, a slit diaphragm component, cause steroid-resistant nephrotic syndrome.
Solanki, Ashish K; Widmeier, Eugen; Arif, Ehtesham; Sharma, Shailza; Daga, Ankana; Srivastava, Pankaj; Kwon, Sang-Ho; Hugo, Hannah; Nakayama, Makiko; Mann, Nina; Majmundar, Amar J; Tan, Wei; Gee, Heon Yung; Sadowski, Caroline E; Rinat, Choni; Becker-Cohen, Rachel; Bergmann, Carsten; Rosen, Seymour; Somers, Michael; Shril, Shirlee; Huber, Tobias B; Mane, Shrikant; Hildebrandt, Friedhelm; Nihalani, Deepak.
Afiliação
  • Solanki AK; Department of Medicine, Nephrology Division, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Widmeier E; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Department of Medicine IV, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Arif E; Department of Medicine, Nephrology Division, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Sharma S; Department of Medicine, Nephrology Division, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Daga A; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Srivastava P; Department of Medicine, Nephrology Division, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Kwon SH; Department of Cellular Biology and Anatomy, Augusta University, Augusta, Georgia, USA.
  • Hugo H; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Nakayama M; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Mann N; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Majmundar AJ; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Tan W; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Gee HY; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA; Department of Pharmacology, Brain Korea 21 Program for Leading Universities & Students (PLUS) Project for Medical Sciences, Yonsei University College of Medicine, Seoul, Korea.
  • Sadowski CE; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Rinat C; Division of Pediatric Nephrology, Shaare Zedek Medical Center, The Hadassah-Hebrew University School of Medicine, Jerusalem, Israel.
  • Becker-Cohen R; Division of Pediatric Nephrology, Shaare Zedek Medical Center, The Hadassah-Hebrew University School of Medicine, Jerusalem, Israel.
  • Bergmann C; Department of Medicine IV, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Rosen S; Department of Pathology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
  • Somers M; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Shril S; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Huber TB; Department of Medicine IV, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany; III Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany; Biological Signalling Studies (BIOSS) Center for Biological Signaling Studies,
  • Mane S; Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, USA.
  • Hildebrandt F; Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA. Electronic address: friedhelm.hildebrandt@childrens.harvard.edu.
  • Nihalani D; Department of Medicine, Nephrology Division, Medical University of South Carolina, Charleston, South Carolina, USA. Electronic address: nihalani@musc.edu.
Kidney Int ; 96(4): 883-889, 2019 10.
Article em En | MEDLINE | ID: mdl-31472902
Steroid-resistant nephrotic syndrome is a frequent cause of chronic kidney disease almost inevitably progressing to end-stage renal disease. More than 58 monogenic causes of SRNS have been discovered and majority of known steroid-resistant nephrotic syndrome causing genes are predominantly expressed in glomerular podocytes, placing them at the center of disease pathogenesis. Herein, we describe two unrelated families with steroid-resistant nephrotic syndrome with homozygous mutations in the KIRREL1 gene. One mutation showed high frequency in the European population (minor allele frequency 0.0011) and this patient achieved complete remission following treatment, but later progressed to chronic kidney disease. We found that mutant KIRREL1 proteins failed to localize to the podocyte cell membrane, indicating defective trafficking and impaired podocytes function. Thus, the KIRREL1 gene product has an important role in modulating the integrity of the slit diaphragm and maintaining glomerular filtration function.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resistência a Medicamentos / Insuficiência Renal Crônica / Glucocorticoides / Proteínas de Membrana / Síndrome Nefrótica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Kidney Int Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resistência a Medicamentos / Insuficiência Renal Crônica / Glucocorticoides / Proteínas de Membrana / Síndrome Nefrótica Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Kidney Int Ano de publicação: 2019 Tipo de documento: Article