From podocyte biology to novel cures for glomerular disease

The podocyte is a key component of the glomerular filtration barrier. Podocyte dysfunction is central to the underlying pathophysiology of many common glomerular diseases, including diabetic nephropathy, glomerulonephritis and genetic forms of nephrotic syndrome. Collectively, these conditions affec...

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Published in:Kidney international Vol. 96; no. 4; p. 850
Main Authors: Torban, Elena, Braun, Fabian, Wanner, Nicola, Takano, Tomoko, Goodyer, Paul R, Lennon, Rachel, Ronco, Pierre, Cybulsky, Andrey V, Huber, Tobias B
Format: Journal Article
Language:English
Published: United States 01.10.2019
ISSN:1523-1755, 1523-1755
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Abstract The podocyte is a key component of the glomerular filtration barrier. Podocyte dysfunction is central to the underlying pathophysiology of many common glomerular diseases, including diabetic nephropathy, glomerulonephritis and genetic forms of nephrotic syndrome. Collectively, these conditions affect millions of people worldwide, and account for the majority of kidney diseases requiring dialysis and transplantation. The 12th International Podocyte Conference was held in Montreal, Canada from May 30 to June 2, 2018. The primary aim of this conference was to bring together nephrologists, clinician scientists, basic scientists and their trainees from all over the world to present their research and to establish networks with the common goal of developing new therapies for glomerular diseases based on the latest advances in podocyte biology. This review briefly highlights recent advances made in understanding podocyte structure and metabolism, experimental systems in which to study podocytes and glomerular disease, disease mediators, genetic and immune origins of glomerulopathies, and the development of novel therapeutic agents to protect podocyte and glomerular injury.
AbstractList The podocyte is a key component of the glomerular filtration barrier. Podocyte dysfunction is central to the underlying pathophysiology of many common glomerular diseases, including diabetic nephropathy, glomerulonephritis and genetic forms of nephrotic syndrome. Collectively, these conditions affect millions of people worldwide, and account for the majority of kidney diseases requiring dialysis and transplantation. The 12th International Podocyte Conference was held in Montreal, Canada from May 30 to June 2, 2018. The primary aim of this conference was to bring together nephrologists, clinician scientists, basic scientists and their trainees from all over the world to present their research and to establish networks with the common goal of developing new therapies for glomerular diseases based on the latest advances in podocyte biology. This review briefly highlights recent advances made in understanding podocyte structure and metabolism, experimental systems in which to study podocytes and glomerular disease, disease mediators, genetic and immune origins of glomerulopathies, and the development of novel therapeutic agents to protect podocyte and glomerular injury.The podocyte is a key component of the glomerular filtration barrier. Podocyte dysfunction is central to the underlying pathophysiology of many common glomerular diseases, including diabetic nephropathy, glomerulonephritis and genetic forms of nephrotic syndrome. Collectively, these conditions affect millions of people worldwide, and account for the majority of kidney diseases requiring dialysis and transplantation. The 12th International Podocyte Conference was held in Montreal, Canada from May 30 to June 2, 2018. The primary aim of this conference was to bring together nephrologists, clinician scientists, basic scientists and their trainees from all over the world to present their research and to establish networks with the common goal of developing new therapies for glomerular diseases based on the latest advances in podocyte biology. This review briefly highlights recent advances made in understanding podocyte structure and metabolism, experimental systems in which to study podocytes and glomerular disease, disease mediators, genetic and immune origins of glomerulopathies, and the development of novel therapeutic agents to protect podocyte and glomerular injury.
The podocyte is a key component of the glomerular filtration barrier. Podocyte dysfunction is central to the underlying pathophysiology of many common glomerular diseases, including diabetic nephropathy, glomerulonephritis and genetic forms of nephrotic syndrome. Collectively, these conditions affect millions of people worldwide, and account for the majority of kidney diseases requiring dialysis and transplantation. The 12th International Podocyte Conference was held in Montreal, Canada from May 30 to June 2, 2018. The primary aim of this conference was to bring together nephrologists, clinician scientists, basic scientists and their trainees from all over the world to present their research and to establish networks with the common goal of developing new therapies for glomerular diseases based on the latest advances in podocyte biology. This review briefly highlights recent advances made in understanding podocyte structure and metabolism, experimental systems in which to study podocytes and glomerular disease, disease mediators, genetic and immune origins of glomerulopathies, and the development of novel therapeutic agents to protect podocyte and glomerular injury.
Author Torban, Elena
Huber, Tobias B
Takano, Tomoko
Goodyer, Paul R
Lennon, Rachel
Ronco, Pierre
Cybulsky, Andrey V
Wanner, Nicola
Braun, Fabian
Author_xml – sequence: 1
  givenname: Elena
  surname: Torban
  fullname: Torban, Elena
  email: elena.torban@mcgill.ca
  organization: Department of Medicine, McGill University Health Centre Research Institute, McGill University, Montreal, Quebec, Canada. Electronic address: elena.torban@mcgill.ca
– sequence: 2
  givenname: Fabian
  surname: Braun
  fullname: Braun, Fabian
  organization: III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
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  givenname: Nicola
  surname: Wanner
  fullname: Wanner, Nicola
  organization: III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
– sequence: 4
  givenname: Tomoko
  surname: Takano
  fullname: Takano, Tomoko
  organization: Department of Medicine, McGill University Health Centre Research Institute, McGill University, Montreal, Quebec, Canada
– sequence: 5
  givenname: Paul R
  surname: Goodyer
  fullname: Goodyer, Paul R
  organization: Department of Pediatrics, McGill University Health Centre Research Institute, McGill University, Montreal, Quebec, Canada
– sequence: 6
  givenname: Rachel
  surname: Lennon
  fullname: Lennon, Rachel
  organization: Wellcome Centre for Cell-Matrix Research, University of Manchester, Manchester, UK
– sequence: 7
  givenname: Pierre
  surname: Ronco
  fullname: Ronco, Pierre
  organization: Sorbonne University, INSERM UMR_S 1155, and Nephrology and Dialysis Department, Hôpital Tenon, Paris France
– sequence: 8
  givenname: Andrey V
  surname: Cybulsky
  fullname: Cybulsky, Andrey V
  organization: Department of Medicine, McGill University Health Centre Research Institute, McGill University, Montreal, Quebec, Canada
– sequence: 9
  givenname: Tobias B
  surname: Huber
  fullname: Huber, Tobias B
  email: t.huber@uke.de
  organization: III. Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. Electronic address: t.huber@uke.de
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