TY - JOUR
T1 - Stimulation of vascular protein synthesis by activation of oestrogen receptor β
AU - Liang, M.
AU - Ekblad, E.
AU - Gustafsson, J. Å
AU - Nilsson, B. O.
PY - 2001
Y1 - 2001
N2 - The objective of this study was to investigate the effects of oestrogen receptor (ER) β activation on vascular protein synthesis and protein expression. Nuclear immuno-reactivity towards ERβ was observed abundantly in vascular smooth muscle and endothelial cells of mouse aorta. No ERα-positive cell nuclei were observed. In aorta from ovariectomized mice, treatment with the selective ERβ agonist genistein (100 nM) for 24 h increased [3H]leucine incorporation by about 30%. This effect was prevented by the ER blocker ICI 182780 (10 μM). Although genistein treatment stimulated protein synthesis, it caused no change in total protein determined either by the Lowry method on tissue homogenate or by densitometric scanning of protein bands (10-220 kDa) separated by SDS-PAGE. Separation of [35S]methionine-labelled proteins by SDS-PAGE did not reveal the protein(s) stimulated by genistein. DNA synthesis was not affected by 100 nM genistein, suggesting that genistein-induced stimulation of protein synthesis is not part of a growth response. Protein expression, determined by SDS-PAGE, was similar in aorta from ERβ-knockout and wild-type mice, suggesting that expression of vascular proteins does not depend solely on a functional ERβ gene. We suggest that activation of vascular ERβ stimulates synthesis of proteins and that this response is not associated with vascular growth.
AB - The objective of this study was to investigate the effects of oestrogen receptor (ER) β activation on vascular protein synthesis and protein expression. Nuclear immuno-reactivity towards ERβ was observed abundantly in vascular smooth muscle and endothelial cells of mouse aorta. No ERα-positive cell nuclei were observed. In aorta from ovariectomized mice, treatment with the selective ERβ agonist genistein (100 nM) for 24 h increased [3H]leucine incorporation by about 30%. This effect was prevented by the ER blocker ICI 182780 (10 μM). Although genistein treatment stimulated protein synthesis, it caused no change in total protein determined either by the Lowry method on tissue homogenate or by densitometric scanning of protein bands (10-220 kDa) separated by SDS-PAGE. Separation of [35S]methionine-labelled proteins by SDS-PAGE did not reveal the protein(s) stimulated by genistein. DNA synthesis was not affected by 100 nM genistein, suggesting that genistein-induced stimulation of protein synthesis is not part of a growth response. Protein expression, determined by SDS-PAGE, was similar in aorta from ERβ-knockout and wild-type mice, suggesting that expression of vascular proteins does not depend solely on a functional ERβ gene. We suggest that activation of vascular ERβ stimulates synthesis of proteins and that this response is not associated with vascular growth.
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U2 - 10.1677/joe.0.1710417
DO - 10.1677/joe.0.1710417
M3 - Article
C2 - 11739007
AN - SCOPUS:0035663283
SN - 0022-0795
VL - 171
SP - 417
EP - 423
JO - Journal of Endocrinology
JF - Journal of Endocrinology
IS - 3
ER -