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鉴定出的椎实螺神经元胞体之间的体外突触形成需要蛋白质合成,但不需要外在生长因子或底物黏附分子。

In vitro synaptogenesis between the somata of identified Lymnaea neurons requires protein synthesis but not extrinsic growth factors or substrate adhesion molecules.

作者信息

Feng Z P, Klumperman J, Lukowiak K, Syed N I

机构信息

Department of Anatomy, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada T2N 4N1.

出版信息

J Neurosci. 1997 Oct 15;17(20):7839-49. doi: 10.1523/JNEUROSCI.17-20-07839.1997.

Abstract

Nerve growth factors, substrate and cell adhesion molecules, and protein synthesis are considered necessary for most developmental programs, including cell proliferation, migration, differentiation, axogenesis, pathfinding, and synaptic plasticity. Their direct involvement in synapse formation, however, has not yet been fully determined. The neurite outgrowth that precedes synaptogenesis is contingent on protein synthesis, the availability of externally supplied growth factors, and substrate adhesion molecules. It is therefore difficult to ascertain whether these factors are also needed for synapse formation. To examine this issue directly we reconstructed synapses between the cell somata of identified Lymnaea neurons. We show that when paired in the presence of brain conditioned medium (CM), mutual inhibitory chemical synapses between neurons right pedal dorsal 1 (RPeD1) and visceral dorsal 4 (VD4) formed in a soma-soma configuration (86%; n = 50). These synapses were reliable and target cell specific and were similar to those seen in the intact brain. To test whether synapse formation between RPeD1 and VD4 required de novo protein synthesis, the cells were paired in the presence of anisomycin (a nonspecific protein synthesis blocker). Chronic anisomycin treatment (18 hr) after cell pairing completely blocked synaptogenesis between RPeD1 and VD4 (n = 24); however, it did not affect neuronal excitability or responsiveness to exogenously applied transmitters (n = 7), nor did chronic anisomycin treatment affect synaptic transmission between pairs of cells that had formed synapses (n = 5). To test the growth and substrate dependence of synapse formation, RPeD1 and VD4 were paired in the absence of CM [defined medium; (n = 22)] on either plain plastic culture dishes (n = 10) or glass coverslips (n = 10). Neither CM nor any exogenous substrate was required for synapse formation. In summary, our data provide direct evidence that synaptogenesis in this system requires specific, cell contact-induced, de novo protein synthesis but does not depend on extrinsic growth factors or substrate adhesion molecules.

摘要

神经生长因子、底物和细胞黏附分子以及蛋白质合成被认为是大多数发育程序所必需的,包括细胞增殖、迁移、分化、轴突形成、路径寻找和突触可塑性。然而,它们是否直接参与突触形成尚未完全确定。突触形成之前的神经突生长取决于蛋白质合成、外部提供的生长因子的可用性以及底物黏附分子。因此,很难确定这些因素对于突触形成是否也是必需的。为了直接研究这个问题,我们在已鉴定的椎实螺神经元的细胞体之间重建了突触。我们发现,当在脑条件培养基(CM)存在的情况下配对时,右足背1(RPeD1)神经元和内脏背4(VD4)神经元之间以体细胞-体细胞构型形成了相互抑制性化学突触(86%;n = 50)。这些突触是可靠的且具有靶细胞特异性,与完整大脑中的突触相似。为了测试RPeD1和VD4之间的突触形成是否需要从头合成蛋白质,细胞在茴香霉素(一种非特异性蛋白质合成阻滞剂)存在的情况下配对。细胞配对后进行慢性茴香霉素处理(18小时)完全阻断了RPeD1和VD4之间的突触形成(n = 24);然而,它并不影响神经元的兴奋性或对外源性应用递质的反应性(n = 7),慢性茴香霉素处理也不影响已形成突触的细胞对之间的突触传递(n = 5)。为了测试突触形成对生长和底物的依赖性,RPeD1和VD4在没有CM [限定培养基;(n = 22)]的情况下,在普通塑料培养皿(n = 10)或玻璃盖玻片(n = 10)上配对。突触形成既不需要CM也不需要任何外源性底物。总之,我们的数据提供了直接证据,表明该系统中的突触形成需要特定的、细胞接触诱导的从头合成蛋白质,但不依赖于外在生长因子或底物黏附分子。

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