Androgens are steroid hormones with a pivotal role in determining male characteristics, which bind to the androgen receptor (AR) to direct a unique transcriptional program. Although best studied in the human prostate and in prostate cancer, the AR transcriptional network also controls normal functions of other male reproductive tract tissues, including the epididymis and the vas deferens. A critical function of the epididymis, the proximal part of the male genital ducts that transport testicular products out of the body, is in sperm maturation. Immature sperm leaving the testis acquire the capacity to fertilize an egg during their passage through the head and body of the epididymis. Many factors contribute to establishing and maintaining the specific epididymis luminal environment that is required for normal sperm maturation. These include hormones and other testicular products that enter the duct, though the epithelium lining the epididymis has a pivotal role. The proximal luminal fluid has a low pH and bicarbonate concentration to preserve sperm motility and relatively high potassium concentrations to facilitate sperm quiescence. Multiple ion channels, ion exchangers, transporters and water channels in the apical or basolateral membranes of the epididymis epithelium participate in fine-tuning the luminal fluid. Building upon a) substantial preliminary data on the AR transcriptional network in human epididymis epithelial (HEE) cells, which suggest novel co-factors for this TF are involved in the epididymis, together with b) an innovative HEE organoid model, our goal is to test the overarching hypothesis that the Androgen Receptor is pivotal to establishing and maintaining normal functions of the human epididymis epithelium. Moreover, that through the recruitment of specific co-factors, AR orchestrates a unique transcriptional program in this tissue. In the first specific aim we will determine the mechanisms through which androgens impact the differentiation and function of the human epididymis epithelium. We will use a novel epididymis organoid model for functional studies together with single cell RNA- sequencing (scRNA-seq). These experiments will provide novel and important insights into the role of androgens in the biology of the human epididymis epithelium and the transcriptional network that coordinates its functions. Studies in the second aim will determine the mechanisms of interaction of AR with other co- factors including RUNX1 and CEBP? and how these factors integrate into the transcriptional network in the human epididymis epithelium. We will also investigate the hierarchy of dependency of AR, RUNX1 and CEBP? using genome wide and locus-specific assays. A gene of particular interest is the cystic fibrosis transmembrane conductance regulator (CFTR), which establishes and maintains chloride and bicarbonate gradients in the epididymis lumen. CFTR recruits a unique set of cis-regulatory elements in HEE cells, some of which also bind AR. These data may facilitate the identification of novel targets for male contraceptives and also have a profound impact on therapeutic approaches to restore male fertility in epididymis disease.
The Androgen receptor has a pivotal role in regulating gene expression in the male reproductive system, though is mainly studied in the prostate epithelium. Here we investigate its unique role in the human epididymis epithelium, which may inform new therapeutic approaches to male contraception and infertility.
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