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aP2-Cre-Mediated In...
aP2-Cre-Mediated Inactivation of Estrogen Receptor Alpha Causes Hydrometra
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- Antonson, P. (författare)
- Karolinska Institutet
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Matic, M. (författare)
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- Portwood, N. (författare)
- Karolinska Institutet
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- Kuiper, R. V. (författare)
- Karolinska Institutet
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- Bryzgalova, G. (författare)
- Karolinska Institutet
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- Gao, H. (författare)
- Karolinska Institutet
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- Windahl, Sara H, 1971 (författare)
- Gothenburg University,Göteborgs universitet,Centre for Bone and Arthritis Research,Institutionen för medicin, avdelningen för invärtesmedicin och klinisk nutrition,Institute of Medicine, Department of Internal Medicine and Clinical Nutrition
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Humire, P. (författare)
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- Ohlsson, Claes, 1965 (författare)
- Gothenburg University,Göteborgs universitet,Institutionen för medicin,Centre for Bone and Arthritis Research,Institute of Medicine
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- Berggren, P. O. (författare)
- Karolinska Institutet
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- Gustafsson, J. A. (författare)
- Karolinska Institutet
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- Dahlman-Wright, K. (författare)
- Karolinska Institutet
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(creator_code:org_t)
- 2014-01-08
- 2014
- Engelska.
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Ingår i: Plos One. - : Public Library of Science (PLoS). - 1932-6203. ; 9:1
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https://gup.ub.gu.se...
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Abstract
Ämnesord
Stäng
- In this study we describe the reproductive phenotypes of a novel mouse model in which Cre-mediated deletion of ER alpha is regulated by the aP2 (fatty acid binding protein 4) promoter. ER alpha-floxed mice were crossed with transgenic mice expressing Cre-recombinase under the control of the aP2 promoter to generate aP2-Cre/ER alpha(flox/flox) mice. As expected, ER alpha mRNA levels were reduced in adipose tissue, but in addition we also detected an 80% reduction of ER alpha levels in the hypothalamus of aP2-Cre/ER alpha(flox/flox) mice. Phenotypic analysis revealed that aP2-Cre/ER alpha(flox/flox) female mice were infertile. In line with this, aP2-Cre/ER alpha(flox/flox) female mice did not cycle and presented 3.8-fold elevated estrogen levels. That elevated estrogen levels were associated with increased estrogen signaling was evidenced by increased mRNA levels of the estrogen-regulated genes lactoferrin and aquaporin 5 in the uterus. Furthermore, aP2-Cre/ER alpha(flox/flox) female mice showed an accumulation of intra-uterine fluid, hydrometra, without overt indications for causative anatomical anomalies. However, the vagina and cervix displayed advanced keratosis with abnormal quantities of accumulating squamous epithelial cells suggesting functional obstruction by keratin plugs. Importantly, treatment of aP2-Cre/ER alpha(flox/flox) mice with the aromatase inhibitor Letrozole caused regression of the hydrometra phenotype linking increased estrogen levels to the observed phenotype. We propose that in aP2-Cre/ER alpha(flox/flox) mice, increased serum estrogen levels cause over-stimulation in the uterus and genital tracts resulting in hydrometra and vaginal obstruction.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Reumatologi och inflammation (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Rheumatology and Autoimmunity (hsv//eng)
Nyckelord
- er-alpha
- hormone neurons
- knockout mice
- deletion
- females
- gene
- beta
- mechanisms
- generation
- phenotypes
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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Plos One
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Till lärosätets databas
- Av författaren/redakt...
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Antonson, P.
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Matic, M.
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Portwood, N.
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Kuiper, R. V.
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Bryzgalova, G.
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Gao, H.
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visa fler...
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Windahl, Sara H, ...
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Humire, P.
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Ohlsson, Claes, ...
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Berggren, P. O.
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Gustafsson, J. A ...
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Dahlman-Wright, ...
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Göteborgs universitet
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Karolinska Institutet