Department of Anatomy and Cell Biology, University of Kansas School of Medicine, Kansas City, Kansas 66160, USA.
Synapse. 2010 Jan;64(1):47-60. doi: 10.1002/syn.20702.
Synapse formation is a well-programmed developmental process involving a variety of cell-cell interactions carried out by distinct groups of molecules. Various molecules that contribute to the assembly of synaptic contacts have been characterized; however, the repertoire of identified proteins expressed by postsynaptic neurons capable of inducing presynaptic differentiation is quite limited. To identify gene transcripts encoding cell surface proteins expressed by postsynaptic cells with molecular features suggestive of synaptogenic activity, this study carried out a genome-wide expression analysis in the chick ciliary ganglion during the different phases of synapse formation. It was found that from the 21,493 gene-probes detected throughout development, 302 protein-coding transcripts were upregulated during the initiation of synapse formation. Analysis of this pool of transcripts showed that 51 of them encoded cell surface proteins (27 membrane-bound and 24 secreted) with protein-protein interacting domains. This includes twelve cell adhesion molecules, six ligand-receptors, six proteins with ligand-like domains, three membrane bound enzymes, eight components of the extracellular matrix, three neuropeptides, three cytokines and growth factors, five extracellular modulators of cell signaling, and five unrelated secreted proteins. Furthermore, the role of synaptic transmission during the initiation of synapse formation was evaluated by assessing the effect of synaptic activity blockade with d-tubocurarine on the expression levels of the pool of 51 transcripts encoding cell surface proteins. Treatment with d-tubocurarine reduced the expression levels of 22% of the selected genes, while the expression levels of 78% of the genes was not affected or was enhanced.
突触形成是一个经过精心编程的发育过程,涉及多种细胞-细胞相互作用,由不同的分子群执行。已经鉴定出许多有助于突触接触组装的分子;然而,能够诱导突触前分化的突触后神经元表达的鉴定蛋白的 repertoire 相当有限。为了鉴定编码具有暗示突触发生活性的分子特征的突触后细胞表面蛋白的基因转录本,本研究在鸡睫状神经节中进行了全基因组表达分析,以研究突触形成的不同阶段。结果发现,在整个发育过程中检测到的 21493 个基因探针中,有 302 个蛋白编码转录本在突触形成的起始阶段上调。对这一转录本池的分析表明,其中 51 个编码细胞表面蛋白(27 个膜结合蛋白和 24 个分泌蛋白),具有蛋白-蛋白相互作用结构域。这包括 12 个细胞黏附分子、6 个配体-受体、6 个具有配体样结构域的蛋白、3 个膜结合酶、8 个细胞外基质成分、3 个神经肽、3 个细胞因子和生长因子、5 个细胞信号转导的细胞外调节剂和 5 个无关的分泌蛋白。此外,通过评估突触活动阻断剂 d-筒箭毒碱对编码细胞表面蛋白的 51 个转录本池的表达水平的影响,评估了突触传递在突触形成起始中的作用。用 d-筒箭毒碱处理降低了所选基因的 22%的表达水平,而 78%的基因的表达水平不受影响或增强。