Literature DB >> 15781987

Expression of the arylhydrocarbon receptor in the peri-implantation period of the mouse uterus and the impact of dioxin on mouse implantation.

Michio Kitajima1, Khaleque Newaz Khan, Akira Fujishita, Hideaki Masuzaki, Takehiko Koji, Tadayuki Ishimaru.   

Abstract

The arylhydrocarbon receptor (AhR) is a nuclear transcription factor mediating toxic effects of chemicals such as dioxins. The 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), a member of polyhalogenated aromatic hydrocarbons family, exerts a wide-variety of toxic effects in a tissue- and species-specific manner including the reproduction process. Recently, AhR-mediated direct effects of TCDD on a cell-specific interaction with ovarian steroids have been shown. However, information regarding the effects of TCDD on the mouse implantation is limited. We therefore examined the expression and localization of AhR in the pregnant mouse uterus from 4 to 10 days of gestation (day 4 to day 10) using immunohistochemistry to investigate the effect of TCDD on uterine tissue during the peri-implantation period. Intense AhR expression was detected in the uterine vasculature throughout the periods examined. We also found that implanted blastocysts and their surrounding luminal epithelia and decidualized stroma expressed AhR on day 5. On days 6 and 7, persistent AhR expression was found in the transitional zone between the invading embryonic tissue and decidual tissue. On days 9 to 10, placental vasculature and spongiotrophoblasts displayed AhR immunoreactivity. The administration of TCDD on day 4 decreased the number of surviving implanted embryos on day 7 in a dose-dependent manner. This effect of TCDD was inhibited by the simultaneous administration of an AhR antagonist, alpha-naphthoflavone (alpha-NF). The spatio-temporal expression of AhR during the peri-implantation phase of the mouse uterus may indicate functional roles of this orphan receptor in fetomaternal interactions as well as substantiate the risk of exposure to chemicals such as dioxins during the reproductive period.

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Year:  2004        PMID: 15781987     DOI: 10.1679/aohc.67.465

Source DB:  PubMed          Journal:  Arch Histol Cytol        ISSN: 0914-9465


  8 in total

1.  Aryl hydrocarbon receptor activation in lactotropes and gonadotropes interferes with estradiol-dependent and -independent preprolactin, glycoprotein alpha and luteinizing hormone beta gene expression.

Authors:  Jinyan Cao; Heather B Patisaul; Sandra L Petersen
Journal:  Mol Cell Endocrinol       Date:  2010-12-25       Impact factor: 4.102

2.  Expression of aryl hydrocarbon receptor in human placentas and fetal tissues.

Authors:  Yi-zhou Jiang; Kai Wang; Roy Fang; Jing Zheng
Journal:  J Histochem Cytochem       Date:  2010-03-30       Impact factor: 2.479

3.  Ah Receptor Signaling Controls the Expression of Cardiac Development and Homeostasis Genes.

Authors:  Vinicius S Carreira; Yunxia Fan; Qing Wang; Xiang Zhang; Hisaka Kurita; Chia-I Ko; Mindi Naticchioni; Min Jiang; Sheryl Koch; Mario Medvedovic; Ying Xia; Jack Rubinstein; Alvaro Puga
Journal:  Toxicol Sci       Date:  2015-07-02       Impact factor: 4.849

Review 4.  Exposure to endocrine disruptors during adulthood: consequences for female fertility.

Authors:  Saniya Rattan; Changqing Zhou; Catheryne Chiang; Sharada Mahalingam; Emily Brehm; Jodi A Flaws
Journal:  J Endocrinol       Date:  2017-03-29       Impact factor: 4.286

Review 5.  The role of the aryl hydrocarbon receptor in the female reproductive system.

Authors:  Isabel Hernández-Ochoa; Bethany N Karman; Jodi A Flaws
Journal:  Biochem Pharmacol       Date:  2008-10-14       Impact factor: 5.858

6.  Treatment of Human Placental Choriocarcinoma Cells with Formaldehyde and Benzene Induced Growth and Epithelial Mesenchymal Transition via Induction of an Antioxidant Effect.

Authors:  Hae-Miru Lee; Soo-Min Kim; Kyung-Chul Choi
Journal:  Int J Environ Res Public Health       Date:  2017-07-29       Impact factor: 3.390

7.  Evaluation of Placentation and the Role of the Aryl Hydrocarbon Receptor Pathway in a Rat Model of Dioxin Exposure.

Authors:  Khursheed Iqbal; Stephen H Pierce; Keisuke Kozai; Pramod Dhakal; Regan L Scott; Katherine F Roby; Carrie A Vyhlidal; Michael J Soares
Journal:  Environ Health Perspect       Date:  2021-11-08       Impact factor: 9.031

Review 8.  Molecular mechanisms of the physiological functions of the aryl hydrocarbon (dioxin) receptor, a multifunctional regulator that senses and responds to environmental stimuli.

Authors:  Yoshiaki Fujii-Kuriyama; Kaname Kawajiri
Journal:  Proc Jpn Acad Ser B Phys Biol Sci       Date:  2010       Impact factor: 3.493

  8 in total

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