Evidence map›Paper›PMID 28808241›Full record

ArticleScientific reports2017

Specific calpain inhibition protects kidney against inflammaging.

Guillaume Hanouna, Laurent Mesnard, Sophie Vandermeersch, Joëlle Perez, Sandrine Placier, Jean-Philippe Haymann, Fabien Campagne, Julien Moroch, Aurélien Bataille, Laurent Baud and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
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

11 authors at 2 institutions in 2 countries.

Guillaume HanounaSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Laurent MesnardSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Sophie VandermeerschSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Joëlle PerezSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Sandrine PlacierSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Jean-Philippe HaymannSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Fabien CampagneThe HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsaud Institute for Computational Biomedicine, Weill Cornell Medical College, New York, United States of America.
Julien MorochDepartment of Physiology and Biophysics, The Weill Cornell Medical College, New York, United States of America.
Aurélien BatailleSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Laurent BaudSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France.
Emmanuel LetavernierSorbonne Universités, UPMC Univ Paris 06, UMR S 1155, F-75020, Paris, France. emmanuel.letavernier@tnn.aphp.fr.
Inserm · FRCornell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calpains are ubiquitous pro-inflammatory proteases, whose activity is controlled by calpastatin, their specific inhibitor. Transgenic mice over-expressing rabbit calpastatin (CalpTG) are protected against vascular remodelling and angiotensin II-dependent inflammation. We hypothesized that specific calpain inhibition would protect against aging-related lesions in arteries and kidneys. We analysed tissues from 2-months and 2-years-old CalpTG and wild-type mice and performed high throughput RNA-Sequencing of kidney tissue in aged mice. In addition, we analysed inflammatory response in the kidney of aged CalpTG and wild-type mice, and in both in vivo (monosodium urate peritonitis) and in vitro models of inflammation. At two years, CalpTG mice had preserved kidney tissue, less vascular remodelling and less markers of senescence than wild-type mice. Nevertheless, CalpTG mice lifespan was not extended, due to the development of lethal spleen tumors. Inflammatory pathways were less expressed in aged CalpTG mice, especially cytokines related to NF-κB and NLRP3 inflammasome activation. CalpTG mice had reduced macrophage infiltration with aging and CalpTG mice produced less IL-1α and IL-1β in vivo in response to inflammasome activators. In vitro, macrophages from CalpTG mice produced less IL-1α in response to particulate activators of inflammasome. Calpains inhibition protects against inflammaging, limiting kidney and vascular lesions related to aging.

Indexed as

AgingAnimalsArteriesCalcium-Binding ProteinsCalpainCells, CulturedCysteine Proteinase InhibitorsCytokinesInflammasomesKidneyMiceMice, Inbred C57BLNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinPeritonitisRabbitsCalcium-Binding ProteinsCalpaincalpastatinCysteine Proteinase InhibitorsCytokinesInflammasomesNF-kappa BNLR Family, Pyrin Domain-Containing 3 ProteinNlrp3 protein, mouse

Identifiers

PMID28808241
PMCPMC5556007
OpenAlexW2744147836

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.