Adipose tissue gene expression of CXCL10 and CXCL11 modulates inflammatory markers in obesity: implications for metabolic inflammation and insulin resistance.

CXCL10 CXCL11 CXCL9 adipose tissue insulin resistance metabolic inflammation obesity

Journal

Therapeutic advances in endocrinology and metabolism
ISSN: 2042-0188
Titre abrégé: Ther Adv Endocrinol Metab
Pays: United States
ID NLM: 101532143

Informations de publication

Date de publication:
2020
Historique:
received: 14 10 2019
accepted: 10 05 2020
entrez: 14 7 2020
pubmed: 14 7 2020
medline: 14 7 2020
Statut: epublish

Résumé

The CXCL subfamily of chemokines (CXCL9, CXCL10, and CXCL11; angiostatic chemokines) plays a key role in many inflammatory diseases. However, the expression of CXCLs in adipose tissue (AT) during obesity and association of these CXCLs with inflammatory markers and insulin resistance are poorly understood. Therefore, this study aimed to investigate the effects of CXCL gene expression on subcutaneous AT inflammatory markers and insulin resistance. Subcutaneous-fat biopsies were collected from 59 nondiabetic (lean/overweight/obese) individuals for RNA isolation. Expression levels of AT CXCL and inflammatory markers were determined by quantitative reverse transcriptase polymerase chain reaction (RT-qPCR). Biomedical parameters in the plasma were measured by enzyme-linked AT CXCL expression was higher in obese compared with lean individuals ( These data suggest that the CXCL family members, specifically CXCL10 and CXCL11, are potential biomarkers for the onset of AT inflammation during obesity.

Sections du résumé

BACKGROUND BACKGROUND
The CXCL subfamily of chemokines (CXCL9, CXCL10, and CXCL11; angiostatic chemokines) plays a key role in many inflammatory diseases. However, the expression of CXCLs in adipose tissue (AT) during obesity and association of these CXCLs with inflammatory markers and insulin resistance are poorly understood. Therefore, this study aimed to investigate the effects of CXCL gene expression on subcutaneous AT inflammatory markers and insulin resistance.
METHODS METHODS
Subcutaneous-fat biopsies were collected from 59 nondiabetic (lean/overweight/obese) individuals for RNA isolation. Expression levels of AT CXCL and inflammatory markers were determined by quantitative reverse transcriptase polymerase chain reaction (RT-qPCR). Biomedical parameters in the plasma were measured by enzyme-linked
RESULTS RESULTS
AT CXCL expression was higher in obese compared with lean individuals (
CONCLUSION CONCLUSIONS
These data suggest that the CXCL family members, specifically CXCL10 and CXCL11, are potential biomarkers for the onset of AT inflammation during obesity.

Identifiants

pubmed: 32655851
doi: 10.1177/2042018820930902
pii: 10.1177_2042018820930902
pmc: PMC7331767
doi:

Types de publication

Journal Article

Langues

eng

Pagination

2042018820930902

Informations de copyright

© The Author(s), 2020.

Déclaration de conflit d'intérêts

Conflict of interest statement: The authors declare that there is no conflict of interest.

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Auteurs

Shihab Kochumon (S)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Ashraf Al Madhoun (AA)

Animal and Imaging Core Facilities, Dasman Diabetes Institute, Dasman, Kuwait.

Fatema Al-Rashed (F)

Immunology and Microbiology Department, Dasman Diabetes Institute, Dasman, Kuwait.

Rafaat Azim (R)

School of Medicine, Royal College of Surgeons in Ireland, Medical University of Bahrain, Busaiteen, Bahrain.

Ebaa Al-Ozairi (E)

Medical Division, Dasman Diabetes Institute, Kuwait.

Fahd Al-Mulla (F)

Genetics and Bioinformatics, Dasman Diabetes Institute, Kuwait, Dasman, Kuwait.

Rasheed Ahmad (R)

Immunology & Microbiology Department, Dasman Diabetes Institute, AL-Soor Street, P.O. Box 1180 Dasman, Kuwait 15462, Kuwait.

Classifications MeSH