Calcium-dependent glutamate release from astrocytes

星形胶质细胞钙依赖性谷氨酸释放

• 批准号: 7252699
• 负责人: VLADIMIR PARPURA
• 金额: $ 6.83万
• 依托单位: UNIVERSITY OF CALIFORNIA RIVERSIDE
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-06-01 至 2007-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7252699
• 关键词: Calcium; dependent; glutamate; release; astrocytes

DESCRIPTION (provided by applicant): Astrocytes, a subtype of glial cell, exhibit a form of excitability based on intracellular Ca2+ variations. These intracellular calcium variations, i.e., oscillations can be evoked by neurotransmitters. The functional consequences of calcium oscillations in astrocytes are poorly understood. Since the level of intracellular calcium ions control glutamate release from astrocytes, we hypothesize that the frequency of calcium oscillations also control the amount of glutamate release from these cells. We will test this hypothesis in Specific Aim I. Calcium-dependent secretion in neurons can be modulated by the protein kinase A (PKA)- and protein kinase C (PKC)-dependent phosphorylation of secretory machinery downstream of calcium. Since astrocytes express the core proteins of the secretory machinery responsible for neuronal secretion, we hypothesize that glutamate release from astrocytes may also be modulated by PKA- and PKC-dependent phosphorylation at the site of secretory machinery. We will test this hypothesis in Specific Aim II. Specific Aim I: We will test the hypothesis that glutamate release from astrocytes is controlled by the frequency of calcium oscillations. Specific Aim Il: We will test the hypothesis that PKA and PKC modulate calcium-dependent glutamate release from astrocytes. This study will provide new and important information on how astrocytes communicate with neurons. Since astrocytes modulate synaptic transmission by releasing glutamate, this new insight into glial action has potential to change the way we think about central nervous system functions and dysfunctions

描述（由申请人提供）：星形胶质细胞是神经胶质细胞的一种亚型，表现出一种基于细胞内 Ca2+ 变化的兴奋性。这些细胞内钙的变化，即振荡，可以由神经递质引起。星形胶质细胞中钙振荡的功能后果尚不清楚。由于细胞内钙离子的水平控制星形胶质细胞的谷氨酸释放，我们假设钙振荡的频率也控制这些细胞的谷氨酸释放量。我们将在特定目标 I 中检验这一假设。神经元中的钙依赖性分泌可以通过钙分泌机制下游的蛋白激酶 A (PKA) 和蛋白激酶 C (PKC) 依赖性磷酸化来调节。由于星形胶质细胞表达负责神经元分泌的分泌机制的核心蛋白，因此我们假设星形胶质细胞释放的谷氨酸也可能受到分泌机制部位的PKA和PKC依赖性磷酸化的调节。我们将在特定目标 II 中检验这一假设。 具体目标一：我们将检验星形胶质细胞谷氨酸释放受钙振荡频率控制的假设。 具体目标 II：我们将检验 PKA 和 PKC 调节星形胶质细胞钙依赖性谷氨酸释放的假设。 这项研究将为星形胶质细胞如何与神经元沟通提供新的重要信息。由于星形胶质细胞通过释放谷氨酸来调节突触传递，这种对神经胶质作用的新见解有可能改变我们对中枢神经系统功能和功能障碍的看法