NEURONAL ACETYLCHOLINE RECEPTOR MECHANISMS

描述：（改编自申请人的摘要） 睫状神经节的电生理、分子和显微镜检查 提出了检验两个假设的技术。 一种假设是， 突触外AChRs影响神经元存活的程度， 在发展过程中成熟。 第二个假设是突触前乙酰胆碱受体，与乙酰胆碱释放有关， 受到神经肽产生的信号的影响， 调节神经末梢释放的手段。 除此之外，还在睫状神经节神经元中发现了α 7 AChR。 相同神经元上的突触a3 AChR。 马焦塔博士提议 通过测量a7来研究a7亚基在发育中的作用 在发展过程中的成绩单，测试的影响， AChR阻断对神经元存活、成熟和突触形成的影响。 突触前乙酰胆碱受体将在培养的和新鲜的 分离神经元并测试它们对ACh释放的影响。 到 检查突触和突触前AChRs是否被不同的 细胞内信号，激活的亚型特异性效应 然后将阐明神经肽的单独信号传导途径。

DESCRIPTION: (adapted from Applicant's Abstract) Studies of the chick ciliary ganglion using electrophysiological, molecular, and microscopic techniques are proposed to test two hypotheses. One hypothesis is that extrasynaptic AChRs influence the extent of neuronal survival and maturation during development. A second hypothesis is that presynaptic AChRs, implicated in ACh release, are influenced by neuropeptide-generated signals thereby providing a means of modulating release from nerve terminals. Alpha7 AChRs have been found in ciliary ganglion neurons in addition to synaptic a3 AChRs on the same neurons. Dr. Margiotta proposes to investigate the role of a7 subunits in development by measuring a7 transcripts during the course of development, testing the effects of AChR blockade on neuron survival, maturation, and synapse formation. Presynaptic AChRs will be sought on terminals of cultured and freshly isolated neurons and tested for their effects on ACh release. To examine if synaptic and presynaptic AChRs are targeted by different intracellular signals, the subtype-specific effects of activating separate signaling pathways by neuropeptides will then be elucidated.