Evidence map›Paper›PMID 41112958›Full record

ArticleFASEB bioAdvances2025

Adipocyte Calpain-2 Deficiency Reduces Obesity-Accelerated Abdominal Aortic Aneurysm Formation in Mice.

Ana Clara Frony, Aida Javidan, Weihua Jiang, Michihiro Okuyama, Lihua Yang, Haruhito A Uchida, Venkateswaran Subramanian

Abstract read
In one paragraph

Article in FASEB bioAdvances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

7 authors.

Ana Clara FronyDivision of Cardiovascular Medicine, Department of Medicine University of Missouri Columbia Missouri USA.ORCID https://orcid.org/0000-0002-0040-3788
Aida JavidanSaha Cardiovascular Research Center University of Kentucky Lexington Kentucky USA.
Weihua JiangSaha Cardiovascular Research Center University of Kentucky Lexington Kentucky USA.
Michihiro OkuyamaSaha Cardiovascular Research Center University of Kentucky Lexington Kentucky USA.
Lihua YangSaha Cardiovascular Research Center University of Kentucky Lexington Kentucky USA.
Haruhito A UchidaDivision of Kidney, Diabetes and Endocrine Diseases Okayama University Medical Development Field Okayama Japan.ORCID https://orcid.org/0000-0002-7629-7678
Venkateswaran SubramanianDivision of Cardiovascular Medicine, Department of Medicine University of Missouri Columbia Missouri USA.ORCID https://orcid.org/0000-0002-1183-7717

Funding

The role of IKKß in linking obesity to adipose tissue inflammation and adipogeneP20GM103527 · NIGMS · UNIVERSITY OF KENTUCKY · PI CASSIS, LISA A · 2012 to 2017
$13.7M
Role of miR-146a in Abdominal Aortic AneurysmR01HL156957 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SUBRAMANIAN, VENKATESWARAN · 2022 to 2025
$2.0M
Calpains and Abdominal Aortic AneurysmsR01HL130086 · NHLBI · UNIVERSITY OF KENTUCKY · PI SUBRAMANIAN, VENKATESWARAN · 2017 to 2020
$1.9M
NHLBI NIH HHS R01 HL130086NHLBI NIH HHS R01 HL156957NIGMS NIH HHS P20 GM103527
6 · The paper itself

Abstract

Abdominal adiposity is associated with increased risk of abdominal aortic aneurysm (AAA) development. Calpains are non-lysosomal calcium-dependent cysteine proteases that are highly expressed in human and experimental AAAs. Using a pharmacological inhibitor and genetically deficient mice, we previously demonstrated that calpain-2 (a major ubiquitous isoform) deficiency mitigated angiotensin II (AngII)-induced AAA formation in hypercholesterolemic mice. In addition, we also demonstrated that calpain inhibition strongly suppressed adipose tissue inflammation in obese mice. Here, we evaluated the contribution of adipocyte-specific calpain-2 on obesity-accelerated AAA in mice. Calpain-2 protein is highly expressed in the periaortic adipose tissue (PAAT) of AngII-induced AAAs in obese mice. To determine the relative contribution of calpain-2 in obesity-accelerated AAA development, calpain-2 floxed mice were bred to mice with a tamoxifen-inducible form of Cre under control of either the ubiquitous promoter, chicken β-actin, or adipocyte-specific promoter, Adipoq. Ubiquitous or adipocyte-specific depletion of calpain-2 in mice significantly suppressed Ang II-induced AAA formation in obese mice. In addition, calpain-2 depletion reduced the incidence of AngII-induced AAAs in mice. Furthermore, calpain-2 deficiency prevented AngII-induced aortic medial elastin fragmentation, adventitial collagen disruption, and periaortic leukocytic accumulation. These results suggest that adipocyte-derived calpain-2 plays a critical role in AngII-induced AAA development in diet-induced obese mice.

Indexed as

abdominal aortic aneurysmadipocytesangiotensin IIcalpainobesity

Identifiers

PMID41112958
PMCPMC12529642

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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.