Mechanism of differential adhesion by protocadherin-cadherin complexes

原钙粘蛋白-钙粘蛋白复合物的差异粘附机制

• 批准号: 8472540
• 负责人: JAMES DAVID JONTES
• 金额: $ 18.3万
• 依托单位: OHIO STATE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-05-24 至 2015-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8472540
• 关键词: Adhesions; Adhesives; Affect; Architecture; Autistic Disorder; Axon; Brain; Cadherins; Cell Adhesion; Cell Adhesion Molecules; Cell Communication; Cell Surface Receptors; Cell physiology; Cells; Complex; Coupled; Data; Development; Disease; Epilepsy; Family; Foundations; Goals; Knowledge; Link; Mediating; Mental Retardation; Molecular; Mutation; N-Cadherin; Nervous system structure; Play; Property; Publishing; Role; Schizophrenia; Testing; Work; cell motility; developmental disease; insight; member; neural circuit; neural patterning; neurodevelopment; neuropsychiatry; novel; preference; protocadherin 19; relating to nervous system; research study; synaptogenesis

DESCRIPTION (provided by applicant): Selective cell-cell interactions are required to establish the precise three-dimensional architecture of the vertebrate nervous system through coordinated cell movements, regional partitioning, axon targeting and synapse formation. The cadherin superfamily comprises a large, diverse array of cell surface receptors that includes both the classical cadherins and the protocadherins. Both classical cadherins and protocadherins have been proposed to play roles in establishing neural circuitry in the developing brain. While the classical cadherins are known to be homophilic cell adhesion molecules, the involvement of protocadherins in cell adhesion remains uncertain. In our previous work, we showed that Protocadherin-19 (Pcdh19) associates with N-cadherin (Ncad) to form a heteromeric cis-complex. In preliminary data, we show that Pcdh19 mediates homophilic adhesion as part of the Pcdh19-Ncad complex, although it is not adhesive itself. The main hypothesis of this proposal is that protocadherins associate with classical cadherins to form cis-complexes with distinct adhesive properties. To investigate this hypothesis in more detail we propose the following Specific Aims. In Aim 1, we will test the hypothesis that members of the d-protocadherin family form cis-complexes with classical cadherins and determine whether these complexes mediate homophilic adhesion, as we have shown for Pcdh19-Ncad. In Aim 2, we will first determine the residues in Pcdh19 that constitute the adhesive interface, and then determine if this mechanism is general to Pcdh-Cdh complexes. Insights gained from these experiments will elucidate the molecular underpinnings of a novel mechanism of cell adhesion and will advance our knowledge of protocadherin and cadherin function, providing an essential foundation for understanding the roles of these molecules in neural development and elucidating the mechanisms that establish patterns of neural connectivity.

描述（由申请人提供）：需要选择性细胞 - 细胞相互作用来通过协调的细胞运动，区域分配，轴突靶向和突触形成来建立脊椎动物神经系统的精确三维结构。钙粘蛋白的超家族包括包括经典钙粘蛋白和原钙粘着蛋白的大量细胞表面受体。经典的钙粘蛋白和原钙粘着蛋白均已提出在发育中的大脑中建立神经回路方面发挥作用。虽然已知经典的钙粘蛋白是均质细胞粘附分子，但原钙粘着蛋白在细胞粘附中的参与仍然不确定。在我们以前的工作中，我们展示了prodocadherin-19（pCDH19）与N-钙粘蛋白（NCAD）相关的，以形成异源顺式顺式复合物。在初步数据中，我们显示PCDH19作为PCDH19-NCAD复合物的一部分介导同型粘附，尽管它本身不是粘合剂。该提议的主要假设是，原钙粘着蛋白与经典的钙粘蛋白相关，形成具有不同粘合特性的顺式复合物。为了详细研究这一假设，我们提出了以下特定目的。在AIM 1中，我们将检验以下假设：D-Protocadherin家族的成员与经典的钙粘蛋白形成顺式复合物，并确定这些复合物是否介导了均电粘附，正如我们为PCDH19-NCAD所示。在AIM 2中，我们将首先确定构成粘合剂界面的PCDH19中的残基，然后确定该机制是否对PCDH-CDH复合物是一般的。从这些实验中获得的见解将阐明一种新型细胞粘附机制的分子基础，并将促进我们对原钙粘蛋白和钙粘蛋白功能的了解，为理解这些分子在神经发育中的作用并阐明建立神经连接模式的机制。