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

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.

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