Evidence map›Paper›PMID 22951891›Full record

ArticleKidney international2012

The IgA1 immune complex-mediated activation of the MAPK/ERK kinase pathway in mesangial cells is associated with glomerular damage in IgA nephropathy.

Houda Tamouza, Jonathan M Chemouny, Leona Raskova Kafkova, Laureline Berthelot, Martin Flamant, Marie Demion, Laurent Mesnard, Etienne Paubelle, Francine Walker, Bruce A Julian and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Kidney international, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

57 citing papers in PubMed, 97 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. N-methyl-D-aspartate receptor inhibition protects against obesity-induced kidney disease.Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association · 2026
    Article
  5. Review
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  15. Article
  16. Review
  17. Article
  18. Article
  19. IgA nephropathy.Nature reviews. Disease primers · 2023
    Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 4 institutions in 3 countries.

Houda TamouzaINSERM U699, Paris, France.
Jonathan M Chemouny
Leona Raskova Kafkova
Laureline Berthelot
Martin Flamant
Marie Demion
Laurent Mesnard
Etienne Paubelle
Francine Walker
Bruce A Julian
Emilie Tissandié
Meetu K Tiwari
Niels O S Camara
François Vrtovsnik
Marc Benhamou
Jan Novak
Renato C Monteiro
Ivan C Moura
Inserm · FRUniversity of Alabama at Birmingham · USAssistance Publique – Hôpitaux de Paris · FRUniversidade de São Paulo · BR

Funding

Elucidating IgA Nephropathy through Genetic Studies of IgA1 GlycosylationR01DK082753 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI GHARAVI, ALI G, NOVAK, JAN · 2009 to 2024
$8.7M
Immune Complexes and Mesangial Cells in IGA NephropathyP01DK061525 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI MESTECKY, JIRI F · 2002 to 2006
$6.7M
Molecular Basis of Pathogenicity of IgA1-containing Immune ComplexesR01DK078244 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI JAN NOVAK · 2007 to 2026
$6.0M
Analytical tools for the analysis of clustered O-glycans in clinical samplesR01GM098539 · NIGMS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI RENFROW, MATTHEW B · 2011 to 2019
$2.7M
Urinary Polypeptide Biomarkers of IgA NephropathyR21DK075868 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NOVAK, JAN · 2009 to 2010
$403k
New Animal Model for Studies of mucosal Immunity and IgA NephropathyR21DK083663 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NOVAK, JAN · 2010 to 2011
$401k
Molecular Basis of Pathogenicity of IgA1-containing Immune ComplexesR56DK078244 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI NOVAK, JAN · 2012 to 2012
$92k
NIDDK NIH HHS DK061525NIDDK NIH HHS DK075868NIDDK NIH HHS DK078244NIDDK NIH HHS DK082753NIDDK NIH HHS DK083663NIDDK NIH HHS P01 DK061525NIDDK NIH HHS R01 DK078244NIDDK NIH HHS R01 DK082753NIDDK NIH HHS R21 DK075868NIDDK NIH HHS R21 DK083663NIDDK NIH HHS R56 DK078244NIGMS NIH HHS GM098539NIGMS NIH HHS R01 GM098539
6 · The paper itself

Abstract

IgA nephropathy (IgAN), the most common primary glomerulonephritis worldwide, has significant morbidity and mortality as 20-40% of patients progress to end-stage renal disease within 20 years of onset. In order to gain insight into the molecular mechanisms involved in the progression of IgAN, we systematically evaluated renal biopsies from such patients. This showed that the MAPK/ERK signaling pathway was activated in the mesangium of patients presenting with over 1 g/day proteinuria and elevated blood pressure, but absent in biopsy specimens of patients with IgAN and modest proteinuria (<1 g/day). ERK activation was not associated with elevated galactose-deficient IgA1 or IgG specific for galactose-deficient IgA1 in the serum. In human mesangial cells in vitro, ERK activation through mesangial IgA1 receptor (CD71) controlled pro-inflammatory cytokine secretion and was induced by large-molecular-mass IgA1-containing circulating immune complexes purified from patient sera. Moreover, IgA1-dependent ERK activation required renin-angiotensin system as its blockade was efficient in reducing proteinuria in those patients exhibiting substantial mesangial activation of ERK. Thus, ERK activation alters mesangial cell-podocyte crosstalk, leading to renal dysfunction in IgAN. Assessment of MAPK/ERK activation in diagnostic renal biopsies may predict the therapeutic efficacy of renin-angiotensin system blockers in IgAN.

Indexed as

Cell CommunicationMAP Kinase Signaling SystemAdultAgedAngiotensin-Converting Enzyme InhibitorsAngiotensin IIAngiotensin II Type 1 Receptor BlockersAntigen-Antibody ComplexAntigens, CDBiopsyBlood PressureCalciumCell ProliferationCells, CulturedEnzyme ActivationExtracellular Signal-Regulated MAP KinasesAngiotensin-Converting Enzyme InhibitorsAngiotensin IIAngiotensin II Type 1 Receptor BlockersAntigen-Antibody ComplexAntigens, CDCalciumCD71 antigenExtracellular Signal-Regulated MAP KinasesIL6 protein, humanImmunoglobulin AInflammation MediatorsInterleukin-6MTOR protein, humanPhosphatidylinositol 3-KinaseProto-Oncogene Proteins c-aktReceptors, TransferrinTOR Serine-Threonine Kinases

Identifiers

PMID22951891
PMCPMC5177564
OpenAlexW1972687707

What OpenQuestion holds

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Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.