Hormonal Regulation of Sertoli Cell Maturation

支持细胞成熟的激素调节

基本信息

批准号：
7370914
负责人：
MICHAEL D GRISWOLD
金额：
$ 29.9万
依托单位：
WASHINGTON STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
1977
资助国家：
美国
起止时间：
1977-08-01 至 2013-02-28
项目状态：
已结题

项目摘要

DESCRIPTION (provided by applicant): The long term goal of this project has been to understand the role of Sertoli cells in spermatogenesis. To achieve this goal, previous studies focused on gene expression and hormonal response of murine Sertoli cells and the interactions of the somatic cells with the germinal cells. The results of these studies have led to a central hypothesis that attempts to explain how Sertoli cells regulate the maturation of spermatogonia and the entry into spermatogenesis and meiosis. Elements of this testable hypothesis include: A) A major functional role of the Sertoli cells is to regulate the spatial and temporal delivery of retinoic acid to spermatogonia. B) Once delivered, the retinoic acid stimulates the undifferentiated spermatogonia to enter into a differentiation pathway and ultimately meiosis. Induction of the gene stra8 is a sensitive and reliable marker of this process. C) The delivery of retinoic acid via the Sertoli cells is a highly regulated process and is ultimately responsible for the establishment of the cycle of the seminiferous epithelium. The experiments to test this hypothesis are organized into three specific aims: Specific aim 1: Determine the kinetics of stra8 induction and the extent to which this induction in germ cells leads to differentiation in vivo and in vitro. Specific aim 2: Determine if, and how, the flow of retinoic acid through the Sertoli cells to the spermatogonia is regulated and resolve which components of the Sertoli cells are key for inducing stra8 in spermatogonia and initiating spermatogonial differentiation. Specific aim 3: Examine the onset of meiosis and establishment of the cycle of the seminiferous epithelium in models where the retinoid metabolism has been perturbed. The hypothesis requires that gonocytes and spermatogonia do not have access to circulating retinoic acid except that which is delivered by the Sertoli cells. Another requirement is that the delivery of retinoic acid to gonocytes or spermatogonia is sufficient to push these cells into the differentiation pathway. This hypothesis suggests a mechanism for entry into meiosis and thus predicts how the cycle of the seminiferous epithelium can be generated and regulated. This research project could potentially determine the molecular mechanisms that initiate spermatogenesis in the male germline and determine the role of the Sertoli cells in that process. Results from these studies could lead to new fundamental approaches to problems relating to male infertility and contraception. This research project could potentially determine the molecular mechanisms that initiate spermatogenesis in the male germline and determine the role of the Sertoli cells in that process. Results from these studies could lead to new fundamental approaches to problems relating to male infertility and contraception.

描述（由申请人提供）：该项目的长期目标是了解支持细胞在精子发生中的作用。为了实现这一目标，之前的研究重点是小鼠支持细胞的基因表达和激素反应以及体细胞与生殖细胞的相互作用。这些研究的结果提出了一个中心假设，试图解释支持细胞如何调节精原细胞的成熟以及进入精子发生和减数分裂。这一可检验假设的要素包括： A) 支持细胞的主要功能作用是调节视黄酸向精原细胞的空间和时间递送。 B) 一旦递送，视黄酸就会刺激未分化的精原细胞进入分化途径并最终减数分裂。基因 stra8 的诱导是该过程的敏感且可靠的标记。 C) 通过支持细胞传递视黄酸是一个高度调控的过程，最终负责生精上皮周期的建立。检验这一假设的实验分为三个具体目标：具体目标 1：确定 stra8 诱导的动力学以及生殖细胞中的这种诱导在体内和体外导致分化的程度。具体目标 2：确定视黄酸通过支持细胞到达精原细胞的流动是否以及如何受到调节，并确定支持细胞的哪些成分对于在精原细胞中诱导 stra8 和启动精原细胞分化至关重要。具体目标 3：在类维生素A代谢受到干扰的模型中检查减数分裂的开始和生精上皮周期的建立。该假说要求生殖母细胞和精原细胞无法获得循环视黄酸，除非支持细胞输送视黄酸。另一个要求是将视黄酸递送至生殖细胞或精原细胞足以推动这些细胞进入分化途径。这一假说提出了进入减数分裂的机制，从而预测了生精上皮的周期如何产生和调节。该研究项目可能会确定启动雄性种系精子发生的分子机制，并确定支持细胞在该过程中的作用。这些研究的结果可能会为男性不育和避孕相关问题带来新的基本方法。该研究项目可能会确定启动雄性种系精子发生的分子机制，并确定支持细胞在该过程中的作用。这些研究的结果可能会为男性不育和避孕相关问题带来新的基本方法。