Article ID Journal Published Year Pages File Type
10803119 Biochimica et Biophysica Acta (BBA) - Molecular Cell Research 2005 17 Pages PDF
Abstract
It is well known that the biological and carcinogenic effects of 17β-estradiol (E2) are mediated via nuclear estrogen receptors (ERs) by regulating nuclear gene expression. Several rapid, non-nuclear genomic effects of E2 are mediated via plasma membrane-bound ERs. In addition, there is accumulating evidence suggesting that mitochondria are also important targets for the action of estrogens and ERs. This review summarized the studies on the effects of estrogens via ERs on mitochondrial structure and function. The potential physiological and pathophysiological implications of deficiency and/or overabundance of these E2/ER-mediated mitochondrial effects in stimulation of cell proliferation, inhibition of apoptosis, E2-mediated cardiovascular and neuroprotective effects in target cells are also discussed.
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Life Sciences Biochemistry, Genetics and Molecular Biology Biochemistry
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