Logo Medical Science Monitor

Call: +1.631.470.9640
Mon - Fri 10:00 am - 02:00 pm EST

Contact Us

Logo Medical Science Monitor Logo Medical Science Monitor Logo Medical Science Monitor

26 January 2024: Lab/In Vitro Research

CTRP13 Mitigates Endothelial Cell Ferroptosis via the AMPK/KLF4 Pathway: Implications for Atherosclerosis Protection

Jie Du 123ABCDEF , Jianjun Wu 12ABC , Youqi Zhang 12CDF , Qi Liu 12CDF , Xing Luo 12ABD , Xingtao Huang 12ABC , Xuedong Wang 12ABC , Fan Yang 12AEF , JingBo Hou 12ABCDEFG*

DOI: 10.12659/MSM.942733

Med Sci Monit 2024; 30:e942733

Figure 6 C1q/tumor necrosis factor-related protein 13 (CTRP13) restored mitochondrial functioning by counteracting oxidized low-density lipoprotein (ox-LDL) effects on the AMPK/KLF4 pathway. The following groups were assessed: (1) Control; (2) ox-LDL; (3) ox-LDL + CTRP13; (4) ox-LDL + CTRP13 + compound C; and (5) ox-LDL + CTRP13 + APTO. (A) Representative fluorescent images of DCFH-DA probe and (B) quantification of intracellular reactive oxygen species (ROS) levels in 5 cell groups. (C) Representative fluorescent JC-1 images for testing the mitochondrial membrane potential in human umbilical vein endothelial cells (HUVECs), aggregates shown in green, and monomers shown in red (scale bars=100 μm). (D) Quantitative analysis of the aggregates to monomers ratio. (E, F) Intracellular glutathione peroxidase 4 (GPX4) levels were depicted by representative immunofluorescence images. The data are expressed as the mean±SD (n=3–4 per group). Statistical power=0.972987, effect size(r)=0.914731. * P<0.05 vs the control group. # P<0.05 vs the ox-LDL group. Fluorescent images were evaluated using Olympus fluorescence microscopy with cellSens Dimension software (Version 1.3 rev, Olympus, Tokyo, Japan), and the positive cells were measured by Image Pro Plus 6.0 (Media Cybernetics, Rockville, MD, USA). GraphPad Prism 9.0 software (La Jolla, USA) was used to analyze the data.

Your Privacy

We use cookies to ensure the functionality of our website, to personalize content and advertising, to provide social media features, and to analyze our traffic. If you allow us to do so, we also inform our social media, advertising and analysis partners about your use of our website, You can decise for yourself which categories you you want to deny or allow. Please note that based on your settings not all functionalities of the site are available. View our privacy policy.

Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750