Environmental arsenic and androgen receptor regulation

环境砷和雄激素受体调节

• 批准号: 7645020
• 负责人: ADENA E ROSENBLATT
• 金额: $ 3.67万
• 依托单位: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-15 至 2011-07-14
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7645020
• 关键词: Androgen Receptor; Androgens; Antigens; Arsenic; Arsenites; Binding; Biological Assay; Characteristics; Dactinomycin; Development; Dose; Electrophoretic Mobility Shift Assay; Exposure to; Fertility; Gene Targeting; Genes; Genetic Transcription; Genitourinary system; Goals; Hormones; Infertility; Ligands; Male Infertility; Malignant neoplasm of prostate; Mediating; Messenger RNA; Modeling; Molecular; Nuclear; Physiologic pulse; Play; Production; Prostate; Proteins; RNA Decay; RNase protection assay; Regulation; Reporter; Reporter Genes; Reverse Transcriptase Polymerase Chain Reaction; Role; Running; Sperm Count Procedure; Sperm Motility; Tissues; Toxic effect; Toxin; Transactivation; Western Blotting; activating transcription factor; body system; cancer cell; chromatin immunoprecipitation; mRNA Expression; male; men; promoter; protein expression; radioligand; receptor; receptor function; sodium arsenite; sperm cell

DESCRIPTION (provided by applicant): Environmental arsenic is a known toxin that has detrimental effects on a variety of organ systems including the male urogenital tract. Increased exposure to environmental arsenic is associated with male infertility. The manifestations of infertility in these men include production of abnormal sperm, decreased sperm counts and decreased sperm mobility. While there is evidence to support the relationship between arsenic and male infertility the exact mechanism is unclear. Androgen receptors (AR) are ligand-activated transcription factors that regulate genes involved in development of the male urogenital tract, secondary sexual characteristics, and sperm production. Since the androgen receptor plays a critical role in male fertility it may be a target of arsenic toxicity in the urogenital tract. We have found that sodium arsenite causes a dose dependent inhibition of AR transcriptional activity. This proposal seeks to assess the effect of sodium arsenite on AR-regulated gene transcription. Three different models of androgen target tissues, TM4 (sertoli), PNT2 (normal prostate), and PCS (prostate cancer) cells, will be used for these studies. Our long- term goal is to elucidate the mechanism by which arsenic may regulate AR activity leading to male infertility.

描述（由申请人提供）：环境砷是一种已知的毒素，对包括男性泌尿生殖道在内的各种器官系统具有有害影响。暴露于环境砷的增加与男性不育有关。这些男性不育的表现包括产生异常精子，精子数量减少和精子活动力下降。虽然有证据支持砷和男性不育之间的关系，但确切的机制尚不清楚。雄激素受体（AR）是一种配体激活的转录因子，调节与男性泌尿生殖道发育、第二性征和精子产生有关的基因。由于雄激素受体在男性生育中起着关键作用，因此它可能是尿生殖道砷毒性的靶点。我们已经发现亚砷酸钠导致AR转录活性的剂量依赖性抑制。该提案旨在评估亚砷酸钠对AR调节的基因转录的影响。这些研究将使用三种不同的雄激素靶组织模型，即TM 4（支持细胞）、PNT 2（正常前列腺）和PCS（前列腺癌）细胞。我们的长期目标是阐明砷可能调节AR活性导致男性不育的机制。