Kallistatin limits abdominal aortic aneurysm by attenuating generation of reactive oxygen species and apoptosis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
31 08 2021
Historique:
received: 24 05 2021
accepted: 20 08 2021
entrez: 1 9 2021
pubmed: 2 9 2021
medline: 9 11 2021
Statut: epublish

Résumé

Inflammation, vascular smooth muscle cell apoptosis and oxidative stress are believed to play important roles in abdominal aortic aneurysm (AAA) pathogenesis. Human kallistatin (KAL; gene SERPINA4) is a serine proteinase inhibitor previously shown to inhibit inflammation, apoptosis and oxidative stress. The aim of this study was to investigate the role of KAL in AAA through studies in experimental mouse models and patients. Serum KAL concentration was negatively associated with the diagnosis and growth of human AAA. Transgenic overexpression of the human KAL gene (KS-Tg) or administration of recombinant human KAL (rhKAL) inhibited AAA in the calcium phosphate (CaPO

Identifiants

pubmed: 34465809
doi: 10.1038/s41598-021-97042-8
pii: 10.1038/s41598-021-97042-8
pmc: PMC8408144
doi:

Substances chimiques

Reactive Oxygen Species 0
Serpins 0
kallistatin 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

17451

Informations de copyright

© 2021. The Author(s).

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Auteurs

Smriti Murali Krishna (SM)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Jiaze Li (J)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Yutang Wang (Y)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.
School of Applied and Biomedical Sciences, Faculty of Science and Technology, Federation University Australia, Horsham, VIC, Australia.

Corey S Moran (CS)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Alexandra Trollope (A)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.
Division of Anatomy, College of Medicine and Dentistry, James Cook University, Townsville, QLD, Australia.

Pacific Huynh (P)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Roby Jose (R)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Erik Biros (E)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia.

Jianxing Ma (J)

Department of Physiology, Health Sciences Centre, University of Oklahoma, Oklahoma City, OK, 73104, USA.

Jonathan Golledge (J)

The Vascular Biology Unit, Queensland Research Centre for Peripheral Vascular Disease, College of Medicine and Dentistry, James Cook University, Townsville, QLD, 4811, Australia. jonathan.golledge@jcu.edu.au.
Department of Vascular and Endovascular Surgery, Townsville University Hospital, Townsville, QLD, Australia. jonathan.golledge@jcu.edu.au.

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