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Human peritoneal tight junction, transporter and channel expression in health and kidney failure, and associated solute transport.
Levai, Eszter; Marinovic, Iva; Bartosova, Maria; Zhang, Conghui; Schaefer, Betti; Jenei, Hanna; Du, Zhiwei; Drozdz, Dorota; Klaus, Günter; Arbeiter, Klaus; Romero, Philipp; Schwenger, Vedat; Schwab, Constantin; Szabo, Attila J; Zarogiannis, Sotirios G; Schmitt, Claus Peter.
Afiliação
  • Levai E; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Marinovic I; Pediatric Center, MTA Center of Excellence, Semmelweis University, Budapest, Hungary.
  • Bartosova M; HUNREN SE Pediatrics and Nephrology Research Group, Budapest, Hungary.
  • Zhang C; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Schaefer B; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Jenei H; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Du Z; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Drozdz D; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Klaus G; Division of Pediatric Nephrology, Center for Pediatric and Adolescent Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
  • Arbeiter K; Jagiellonian University Medical College, Krakow, Poland.
  • Romero P; KfH Pediatric Kidney Center, Marburg, Germany.
  • Schwenger V; Department of Pediatrics and Adolescent Medicine, Medical University Vienna, Vienna, Austria.
  • Schwab C; Division of Pediatric Surgery, Department of General, Visceral and Transplantation Surgery, University Hospital Heidelberg, Heidelberg, Germany.
  • Szabo AJ; Department of Nephrology, Klinikum der Landeshauptstadt Stuttgart, Stuttgart, Germany.
  • Zarogiannis SG; Institute of Pathology, Heidelberg University, Heidelberg, Germany.
  • Schmitt CP; Pediatric Center, MTA Center of Excellence, Semmelweis University, Budapest, Hungary.
Sci Rep ; 13(1): 17429, 2023 10 13.
Article em En | MEDLINE | ID: mdl-37833387
Next to the skin, the peritoneum is the largest human organ, essentially involved in abdominal health and disease states, but information on peritoneal paracellular tight junctions and transcellular channels and transporters relative to peritoneal transmembrane transport is scant. We studied their peritoneal localization and quantity by immunohistochemistry and confocal microscopy in health, in chronic kidney disease (CKD) and on peritoneal dialysis (PD), with the latter allowing for functional characterizations, in a total of 93 individuals (0-75 years). Claudin-1 to -5, and -15, zonula occludens-1, occludin and tricellulin, SGLT1, PiT1/SLC20A1 and ENaC were consistently detected in mesothelial and arteriolar endothelial cells, with age dependent differences for mesothelial claudin-1 and arteriolar claudin-2/3. In CKD mesothelial claudin-1 and arteriolar claudin-2 and -3 were more abundant. Peritonea from PD patients exhibited increased mesothelial and arteriolar claudin-1 and mesothelial claudin-2 abundance and reduced mesothelial and arteriolar claudin-3 and arteriolar ENaC. Transperitoneal creatinine and glucose transport correlated with pore forming arteriolar claudin-2 and mesothelial claudin-4/-15, and creatinine transport with mesothelial sodium/phosphate cotransporter PiT1/SLC20A1. In multivariable analysis, claudin-2 independently predicted the peritoneal transport rates. In conclusion, tight junction, transcellular transporter and channel proteins are consistently expressed in peritoneal mesothelial and endothelial cells with minor variations across age groups, specific modifications by CKD and PD and distinct associations with transperitoneal creatinine and glucose transport rates. The latter deserve experimental studies to demonstrate mechanistic links.Clinical Trial registration: The study was performed according to the Declaration of Helsinki and is registered at www.clinicaltrials.gov (NCT01893710).
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Insuficiência Renal Crônica Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Insuficiência Renal / Insuficiência Renal Crônica Idioma: En Ano de publicação: 2023 Tipo de documento: Article