TY - JOUR
T1 - Estrogen receptor-α in osteocytes is important for trabecular bone formation in male mice
AU - Windahl, Sara H.
AU - Börjesson, Anna E.
AU - Farman, Helen H.
AU - Engdahl, Cecilia
AU - Movérare-Skrtic, Sofia
AU - Sjögrena, Klara
AU - Lagerquist, Marie K.
AU - Kindblom, Jenny M.
AU - Koskela, Antti
AU - Tuukkanen, Juha
AU - Pajevic, Paola Divieti
AU - Feng, Jian Q.
AU - Dahlman-Wright, Karin
AU - Antonson, Per
AU - Gustafsson, Jan Åke
AU - Ohlsson, Claes
PY - 2013/2/5
Y1 - 2013/2/5
N2 - The bone-sparing effect of estrogen in both males and females is primarily mediated via estrogen receptor-α (ERα), encoded by the Esr1 gene. ERα in osteoclasts is crucial for the trabecular bonesparing effect of estrogen in females, but it is dispensable for trabecular bone in male mice and for cortical bone in both genders. We hypothesized that ERα in osteocytes is important for trabecular bone in male mice and for cortical bone in both males and females. Dmp1-Cre mice were crossed with ERαflox/flox mice to generate mice lacking ERα protein expression specifically in osteocytes (Dmp1-ERα-/-). Male Dmp1-ERα-/- mice displayed a substantial reduction in trabecular bone volume (-20%, P < 0.01) compared with controls. Dynamic histomorphometry revealed reduced bone formation rate (-45%, P < 0.01) but the number of osteoclasts per bone surface was unaffected in the male Dmp1-ERα-/- mice. The male Dmp1-ERα-/- mice had reduced expression of several osteoblast/osteocyte markers in bone, including Runx2, Sp7, and Dmp1 (P < 0.05). Gonadal intact Dmp1-ERα-/- female mice had no significant reduction in trabecular bone volume but ovariectomized Dmp1-ERα-/- female mice displayed an attenuated trabecular bone response to supraphysiological E2 treatment. Dmp1-ERα-/- mice of both genders had unaffected cortical bone. In conclusion, ERα in osteocytes regulates trabecular bone formation and thereby trabecular bone volume in male mice but it is dispensable for the trabecular bone in female mice and the cortical bone in both genders. We propose that the physiological trabecular bone-sparing effect of estrogen is mediated via ERα in osteocytes in males, but via ERα in osteoclasts in females.
AB - The bone-sparing effect of estrogen in both males and females is primarily mediated via estrogen receptor-α (ERα), encoded by the Esr1 gene. ERα in osteoclasts is crucial for the trabecular bonesparing effect of estrogen in females, but it is dispensable for trabecular bone in male mice and for cortical bone in both genders. We hypothesized that ERα in osteocytes is important for trabecular bone in male mice and for cortical bone in both males and females. Dmp1-Cre mice were crossed with ERαflox/flox mice to generate mice lacking ERα protein expression specifically in osteocytes (Dmp1-ERα-/-). Male Dmp1-ERα-/- mice displayed a substantial reduction in trabecular bone volume (-20%, P < 0.01) compared with controls. Dynamic histomorphometry revealed reduced bone formation rate (-45%, P < 0.01) but the number of osteoclasts per bone surface was unaffected in the male Dmp1-ERα-/- mice. The male Dmp1-ERα-/- mice had reduced expression of several osteoblast/osteocyte markers in bone, including Runx2, Sp7, and Dmp1 (P < 0.05). Gonadal intact Dmp1-ERα-/- female mice had no significant reduction in trabecular bone volume but ovariectomized Dmp1-ERα-/- female mice displayed an attenuated trabecular bone response to supraphysiological E2 treatment. Dmp1-ERα-/- mice of both genders had unaffected cortical bone. In conclusion, ERα in osteocytes regulates trabecular bone formation and thereby trabecular bone volume in male mice but it is dispensable for the trabecular bone in female mice and the cortical bone in both genders. We propose that the physiological trabecular bone-sparing effect of estrogen is mediated via ERα in osteocytes in males, but via ERα in osteoclasts in females.
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U2 - 10.1073/pnas.1220811110
DO - 10.1073/pnas.1220811110
M3 - Article
C2 - 23345419
AN - SCOPUS:84873452045
SN - 0027-8424
VL - 110
SP - 2294
EP - 2299
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 6
ER -