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Regulation of Signaling in Osteoclast Bone Resorption

破骨细胞骨吸收中信号传导的调节

基本信息

批准号：
7257298
负责人：
MEENAKSHI A CHELLAIAH
金额：
$ 28.83万
依托单位：
UNIVERSITY OF MARYLAND BALTIMORE
依托单位国家：
美国
项目类别：
财政年份：
1999
资助国家：
美国
起止时间：
1999-08-01 至 2009-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7257298
关键词：
Actins Applications Grants Binding Binding Proteins Binding Sites Biological Bone Resorption Bone remodeling Complex Degenerative polyarthritis Development Disease Dominant-Negative Mutation Gelsolin Goals Knockout Mice Laboratories Localized Mediating Molecular Mus Non-Receptor Type 12 Protein Tyrosine Phosphatase Oligopeptides Osteoclasts Osteoporosis PTK2B gene PTPN12 gene Pathway interactions Peptides Periodontal Diseases Phosphatidylinositols Phosphoproteins Phosphoric Monoester Hydrolases Phosphorylation Phosphotransferases Proline-Rich Domain Protein Dephosphorylation Protein Kinase Protein Tyrosine Kinase Protein Tyrosine Phosphatase Proteins Regulation Role Signal Transduction Signaling Molecule Signaling Protein Therapeutic Intervention Tyrosine Phosphorylation Wiskott-Aldrich Syndrome adenoviral-mediated design human PTK2B protein monomer phosphatase inhibitor polymerization protein activation protein protein interaction research study rho GTP-Binding Proteins src-Family Kinases treatment effect

项目摘要

DESCRIPTION (provided by applicant): The long-term objective of this proposal is to elucidate the molecular mechanisms involved in actin ring formation and bone resorption. Bone resorption is the first step in bone remodeling. Actin ring formation has been shown to be a prerequisite for efficient bone resorption in osteoclasts. Recent preliminary studies from our laboratory suggest that N-WASP-Arp2/3 complex may have a role in the osteoclast actin ring formation. Tyrosine kinases such as PYK2 and Src are involved in the phosphorylation of N-WASP and N-WASP associated phosphoproteins. Moreover, tyrosine phosphatase (PTP-PEST) has a unique role in the modulation of tyrosine phosphorylation of N-WASP and the associated signaling molecules. We therefore hypothesize: 1. N-WASP coordinately activated by Cdc42, PtdIns P2 (PIP2), and kinase(s) can stimulate Arp2/3 mediated actin polymerization and actin ring formation in osteoclasts. 2. Src/PTP-PEST regulation of tyrosine phosphorylation of N-WASP and the associated signaling proteins is required for actin remodeling in the actin ring and bone resorption. Thus, our Specific Aims are to: 1. Determine the signal transduction mechanisms involved in N-WASP activation and actin ring formation. 2. Determine the regulation of tyrosine phosphorylation, actin ring formation, and bone resorption by PTP-PEST. The goal of this revised renewal application is to identify the underlying molecular mechanisms in actin ring formation. To advance the understanding of the mechanisms of bone resorption at the cellular and molecular level, different approaches will be used. HIV-TAT or adenoviral-mediated delivery of N-WASP, PTP-PEST, and kinases (Src and PYK2) into osteoclasts will be performed to identify the signal transduction mechanisms involved in the formation of N-WASP-Arp2/3 complex and actin ring. The binding sites of PTP-PEST with N-WASP will be characterized by the delivery of TAT-fused oligopeptides derived from proline-rich regions of PTP-PEST and N-WASP. We will analyze the effects of the above-mentioned treatments on actin ring formation and bone resorption. Identification of peptides that impede osteoclast function will be useful in the development of pharmacological agents, targeting osteoclast actin ring formation and bone resorption in disorders such as osteoporosis, periodontal disease, and osteoarthritis.

描述（由申请人提供）：该提案的长期目标是阐明肌动蛋白环形成和骨吸收所涉及的分子机制。骨吸收是骨重塑的第一步。肌动蛋白环的形成已被证明是破骨细胞有效骨吸收的先决条件。我们实验室最近的初步研究表明，N-WASP-Arp2/3 复合物可能在破骨细胞肌动蛋白环的形成中发挥作用。酪氨酸激酶如 PYK2 和 Src 参与 N-WASP 和 N-WASP 相关磷蛋白的磷酸化。此外，酪氨酸磷酸酶（PTP-PEST）在调节 N-WASP 酪氨酸磷酸化和相关信号分子方面具有独特的作用。因此，我们假设： 1. Cdc42、PtdIns P2 (PIP2) 和激酶协同激活的 N-WASP 可以刺激破骨细胞中 Arp2/3 介导的肌动蛋白聚合和肌动蛋白环形成。 2. Src/PTP-PEST 对 N-WASP 酪氨酸磷酸化和相关信号蛋白的调节是肌动蛋白环中肌动蛋白重塑和骨吸收所必需的。因此，我们的具体目标是： 1. 确定参与 N-WASP 激活和肌动蛋白环形成的信号转导机制。 2.确定PTP-PEST对酪氨酸磷酸化、肌动蛋白环形成和骨吸收的调节。这一修订后的更新申请的目标是确定肌动蛋白环形成的潜在分子机制。为了在细胞和分子水平上促进对骨吸收机制的理解，将使用不同的方法。将进行 HIV-TAT 或腺病毒介导的 N-WASP、PTP-PEST 和激酶（Src 和 PYK2）递送至破骨细胞中，以鉴定参与 N-WASP-Arp2/3 复合物和肌动蛋白环形成的信号转导机制。 PTP-PEST 与 N-WASP 的结合位点将通过递送源自 PTP-PEST 和 N-WASP 富含脯氨酸的区域的 TAT 融合寡肽来表征。我们将分析上述治疗对肌动蛋白环形成和骨吸收的影响。鉴定阻碍破骨细胞功能的肽将有助于药物制剂的开发，针对骨质疏松症、牙周病和骨关节炎等疾病中的破骨细胞肌动蛋白环形成和骨吸收。