Related Experiment Video
Updated: May 31, 2026

An In vitro Model to Study Heterogeneity of Human Macrophage Differentiation and Polarization
Published on: June 12, 2013
17β-estradiol inhibits oxidized low-density lipoprotein-induced increase in matrix metalloproteinase-9 expression in
Hiroyasu Uzui1, Satyesh K Sinha, Tripathi B Rajavashisth
1Cardiometabolic Research Unit, Division of Endocrinology, Metabolism and Molecular Medicine, Charles R. Drew University of Medicine and Science, Los Angeles, CA, USA. huzui@u-fukui.ac.jp
Abstract:
Beneficial effects of estrogen have been attributed to improved lipid profiles and to direct effects on the arterial wall. Macrophage-derived matrix metalloproteinases (MMPs) are expressed in atherosclerotic plaques, where they may contribute to plaque disruption. We have shown that oxidized low-density lipoprotein (Ox-LDL) increases matrix metalloproteinase-9 (MMP-9) expression in macrophages (Mφ). In this study, we tested the hypothesis that 17β-estradiol regulates basal and Ox-LDL-induced expression of MMPs and their tissue inhibitor (TIMPs) in human Mφ. Peripheral blood mononuclear cells isolated from normal human subjects were cultured for 7 days to transform into Mφ. On day 7, Mφ were starved with serum-free medium for 16 hours and then treated with 17β-estradiol and/or progesterone (PROG) in the presence or absence Ox-LDL for 24 hours. Levels and activity of MMP-2 and MMP-9 and levels of TIMP-1 and TIMP-2 were determined. After exposure to Ox-LDL, MMP-9 expression increased by 60% and TIMP-1 expression decreased by 29% (P < 0.05 and P < 0.05, respectively, compared to control), whereas TIMP-2 expression was unchanged. 17β-estradiol reduced the levels of Ox-LDL-induced MMP-9 protein as measured by Western blot (P < 0.05; n = 5) and Ox-LDL-induced MMP-9 activity (P < 0.05; n = 5) as measured by gelatin zymography. Conclusively, estradiol abolished Ox-LDL-stimulated increase in the levels of macrophage-derived MMP-9 protein and activity in human Mφ. This effect was reversed by TAM but not by PROG. These data suggest that at least part of the protective effect of estrogen occurs by attenuation of Ox-LDL alterations in MMP-9 expression.
Insights
Estrogen reduces oxidized LDL-induced MMP-9 in macrophages, suggesting a protective role in atherosclerosis. This finding highlights estrogen
Area of Science:
- Cardiovascular Biology
- Endocrinology
- Molecular Medicine
Background:
- Estrogen's cardioprotective effects may involve improved lipid profiles and direct arterial actions.
- Macrophage-derived matrix metalloproteinases (MMPs) are implicated in atherosclerotic plaque instability.
- Oxidized low-density lipoprotein (Ox-LDL) is known to upregulate matrix metalloproteinase-9 (MMP-9) in macrophages.
Purpose of the Study:
- To investigate the regulation of MMPs and tissue inhibitors of metalloproteinases (TIMPs) by 17β-estradiol in human macrophages.
- To determine if 17β-estradiol modulates Ox-LDL-induced MMP expression and activity.
Main Methods:
- Human peripheral blood mononuclear cells were differentiated into macrophages.
- Macrophages were treated with 17β-estradiol and/or progesterone in the presence or absence of Ox-LDL.
- MMP-2, MMP-9, TIMP-1, and TIMP-2 levels and activity were assessed using Western blot and gelatin zymography.
Main Results:
- Ox-LDL significantly increased MMP-9 expression and activity while decreasing TIMP-1 levels.
- 17β-estradiol attenuated Ox-LDL-induced MMP-9 protein levels and activity.
- The effect of 17β-estradiol was reversed by tamoxifen but not by progesterone.
Conclusions:
- 17β-estradiol effectively counteracts Ox-LDL-stimulated MMP-9 upregulation in human macrophages.
- Estrogen's atheroprotective mechanisms may involve the suppression of macrophage-derived MMP-9.
- These findings suggest a role for estrogen in stabilizing atherosclerotic plaques by modulating MMP activity.
More Related Videos
06:18An In Vivo Estrogen Deficiency Mouse Model for Screening Exogenous Estrogen Treatments of Cardiovascular Dysfunction After Menopause
Published on: August 13, 2019
07:29Cell-free Biochemical Fluorometric Enzymatic Assay for High-throughput Measurement of Lipid Peroxidation in High Density Lipoprotein
Published on: October 12, 2017