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CD147 Levels in Blood and Adipose Tissues Correlate with Vascular Dysfunction in Obese Diabetic Adults.

Authors :
Ali MM
Mirza I
Naquiallah D
Hassan C
Masrur M
Bianco FM
Mahmoud AM
Source :
Journal of cardiovascular development and disease [J Cardiovasc Dev Dis] 2021 Dec 28; Vol. 9 (1). Date of Electronic Publication: 2021 Dec 28.
Publication Year :
2021

Abstract

CD147 is a glycoprotein that stimulates the production of matrix metalloproteinases (MMPs), known contributors to cardiovascular risk. The activity of CD147 protein depends on its glycosylation. However, it is unclear whether CD147 protein expression or glycosylation are influenced by the diabetic milieu characterized by hyperglycemia and abundant glycation-end-products (AGEs). We examined the circulating and visceral adipose tissue (VAT) levels of CD147 and their correlation with vascular function in obese, obese diabetic, and non-obese controls ( n = 40, each). The circulating levels of CD147 and the glycosylated CD147 protein in VAT were considerably higher in obese, particularly obese diabetic subjects compared to controls. Obese diabetics had the lowest brachial and arteriolar vasoreactivity and the highest carotid pulse-wave velocity (PWV, a measure of arterial stiffness) among the three groups. CD147 correlated positively with body mass index (BMI), total and visceral fat mass, PWV, and plasma levels of glucose, insulin, MMPs, and AGEs and negatively with brachial artery and VAT-arteriolar vasoreactivity and nitric oxide production. Multivariate regression revealed that BMI, body fat mass, insulin, and glucose levels significantly predicted CD147. Our data suggest that higher levels of CD147 in obese subjects, particularly those with diabetes, are linked to vascular dysfunction and several cardiometabolic risk factors.

Details

Language :
English
ISSN :
2308-3425
Volume :
9
Issue :
1
Database :
MEDLINE
Journal :
Journal of cardiovascular development and disease
Publication Type :
Academic Journal
Accession number :
35050217
Full Text :
https://doi.org/10.3390/jcdd9010007