Estrogen and Aging effects on Transvaginal Transport

雌激素和衰老对经阴道运输的影响

• 批准号: 7233575
• 负责人: GEORGE I GORODESKI
• 金额: $ 35.79万
• 依托单位: CASE WESTERN RESERVE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-06-01 至 2009-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7233575
• 关键词: Actins; Biochemical; Biological Assay; Cell Fractionation; Cells; Communicable Diseases; Complex; Confocal Microscopy; Cultured Cells; Cytoskeleton; Data; Dimerization; Electrophysiology (science); Energy Transfer; Epithelial Cells; Epithelium; Estrogen Replacement Therapy; Estrogens; Exocervix; Extracellular Space; F-Actin; Female; Filament; Fluids and Secretions; Fluoroscopy; Functional disorder; G Actin; Genital system; Grant; Health; Homodimerization; Human; Immunoblotting; Immunofluorescence Immunologic; Immunoprecipitation; Inflammatory; Lateral; Measurement; Measures; Mediating; Menopause; Methodology; Methods; Modeling; Molecular Biology; Motor; Muscle Rigidity; Myosin ATPase; Myosin Heavy Chains; Myosin Type I; Myosin Type II; Nonmuscle Myosin Type IIB; Operative Surgical Procedures; Pathway interactions; Permeability; Phase; Phosphoric Monoester Hydrolases; Phosphorylation; Phosphotransferases; Physiology; Postmenopause; Premenopause; Progress Reports; Proteins; Regulation; Reproduction; Resistance; Rho-associated kinase; Shapes; Signal Pathway; Site-Directed Mutagenesis; Specimen; Structure; System; Takeda brand of pioglitazone hydrochloride; Time; Vagina; Width; Woman; Women' s Health; age effect; age related; base; casein kinase II; human tissue; improved; novel; reproductive; research study; yeast two hybrid system

DESCRIPTION (provided by applicant): Our long-term objective is to understand the mechanisms that regulate the permeability of epithelia of the female reproductive tract. We have discovered that estrogen modulates the Resistance of the Lateral Intercellular Space (R-LIS) of human normal ectocervical-vaginal epithelial cells (ECVE), and decreases the paracellular resistance. The geometry of the lateral intercellular space (and the R-LIS) is determined by the shape of epithelial cells that define this space, and depends on the rigidity of the cytoskeleton. Based on novel preliminary results we advance our Maior Hypothesis that estrogen decreases the rigidity of the cytoskeleton by remodeling the cortical acto-myosin frame. The study has four Specific Aims: (1) To understand how estrogen remodels the cytoskeletal cortical acto-myosin frame. Our Hypothesis-A is that formation of a rigid cortical frame depends on the interaction of nonmuscle myosin IIB with cortical actin. We propose that estrogen remodels the cytoskeleton into a flexible structure by inducing disassembly of nonmusele myosin lIB from the cortical actin ring. (2) To understand the structural basis of the cortical acto-myosin cytoskeletal ring in epithelial cells. Our Hypothesis-B is that in epithelial cells the stability of the cortical myosin-actin ring depends on the interaction of actin with homodimerized nonmuscle myosin IIB filaments. We propose that dedimerization of nonmuscle myosin IIB heavy chains inhibits myosin MgATPase activity, and leads to disassociation of nonmuscle myosin IIB from the cortical acto-myosin frame. (3) To understand the mechanism by which phosphorylation of nonmuscle myosin IIB heavy chains regulates MgATPase activity. Our Hypothesis-C is that that phosphorylation of nonmuscle myosin IIB heavy chains inhibits homodimerization of myosin filaments and blocks myosin MgATPase. The alternative hypothesis is that MgATPase can be regulated independent of dimerization, by phosphorylation of nonmuscle myosin lIB heavy chains directly at the motor domain. (4) To understand the signaling pathway of the estrogen-induced phosphorylation of nonmuscle myosin IIB heavy chains. Our Hypothesis-D is that the effect of estrogen is initiated by activation of the EGFR-MAPK pathway, and it involves casein kinase II (CKII) as the terminal kinase. The extended hypothesis postulates involvement of multimolecular complexes, including Rho-kinase and an unidentified phosphatase, as modulators of CKII-induced phosphorylation of nonmuscle myosin IIB heavy chains. Experiments will utilize tissues of human ectocervix and vagina obtained from women undergoing surgery, and cultures of human ECVE cells grown on filters. Health relatedness of the project: The results of the study may provide novel data about estrogen regulation of the permeability of the female reproductive tract epithelia, and improve our understanding of the physiology of reproduction: the pathophysiology of inflammatory and infectious disease in the genital tract; and for improving woman's health.

描述（由申请人提供）：我们的长期目标是了解调节女性生殖道上皮细胞渗透性的机制。我们发现雌激素调节人正常子宫颈阴道上皮细胞（ECVE）的细胞间间隙阻力（R-LIS），降低细胞旁阻力。侧细胞间隙（和R-LIS）的几何形状由限定该间隙的上皮细胞的形状决定，并取决于细胞骨架的刚性。基于新的初步结果，我们提出了我们的Maior假说，即雌激素通过重塑皮质肌动蛋白-肌球蛋白框架来降低细胞骨架的刚性。本研究有四个具体目的：（1）了解雌激素如何重塑细胞骨架皮质肌动蛋白框架。我们的假设A是，一个刚性的皮质框架的形成依赖于非肌肉肌球蛋白IIB与皮质肌动蛋白的相互作用。我们认为，雌激素通过诱导非肌球蛋白LIB从皮质肌动蛋白环上解体，将细胞骨架重塑成一个灵活的结构。(2)了解上皮细胞中皮质肌动球蛋白细胞骨架环的结构基础。我们的假设B是，在上皮细胞中，皮质肌球蛋白-肌动蛋白环的稳定性取决于肌动蛋白与同型二聚化非肌球蛋白IIB细丝的相互作用。我们建议，去二聚化的非肌肉肌球蛋白IIB重链抑制肌球蛋白MgATP酶活性，并导致非肌肉肌球蛋白IIB从皮质肌动蛋白肌球蛋白框架的解离。(3)了解非肌肉肌球蛋白IIB重链磷酸化调节MgATP酶活性的机制。我们的假设C是，非肌肉肌球蛋白IIB重链的磷酸化抑制肌球蛋白丝的同源二聚化，并阻断肌球蛋白MgATPase。另一种假设是，MgATP酶可以调节独立的二聚化，直接在电机域的非肌肉肌球蛋白IIB重链的磷酸化。(4)了解雌激素诱导的非肌肉肌球蛋白IIB重链磷酸化的信号通路。我们的假说-D是雌激素的作用是通过激活EGFR-MAPK途径启动的，它涉及酪蛋白激酶II（CKII）作为末端激酶。扩展的假设假设涉及多分子复合物，包括Rho激酶和一种身份不明的磷酸酶，作为CKII诱导的非肌肉肌球蛋白IIB重链磷酸化的调节剂。实验将利用从接受手术的妇女获得的人外宫颈和阴道组织，以及在过滤器上生长的人ECVE细胞培养物。该项目的健康相关性：该研究的结果可能提供有关雌激素调节女性生殖道上皮细胞渗透性的新数据，并提高我们对生殖生理学的理解：生殖道炎症和感染性疾病的病理生理学;并改善妇女的健康。