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SNAP-25 缺陷性丘脑皮质纤维在异时性器官型共培养物中的终止和初始分支形成。

Termination and initial branch formation of SNAP-25-deficient thalamocortical fibres in heterochronic organotypic co-cultures.

机构信息

Department of Physiology, Anatomy and Genetics, Le Gros Clark Building, University of Oxford, South Parks Road, Oxford OX1 3QX, UK.

出版信息

Eur J Neurosci. 2012 May;35(10):1586-94. doi: 10.1111/j.1460-9568.2012.08120.x.

Abstract

We are interested in the role of neural activity mediated through regulated vesicular release in the stopping and early branching of the thalamic projections in the cortex. Axon outgrowth, arrival at the cortical subplate, side-branch formation during the waiting period and cortical plate innervation of embryonic thalamocortical projections occurs without major abnormalities in the absence of regulated release in Snap25 (-/-) null mutant mice [Washbourne et al. (2002) Nat. Neurosci. 5:19-26; Molnár et al. (2002) J. Neurosci. 22:10313-10323]. The fact that Snap25 (-/-) null mutant mice die at birth limited our previous experiments to the prenatal period. We therefore investigated the behaviour of thalamic projections in co-culture paradigms by using heterochronic thalamic [embryonic day (E)16-E18] and cortical [postnatal day (P)0-P3] explants, in which the stopping and branching behaviour has been previously documented. Our current co-culture experiments established that thalamic projections from E16-E18 Snap25(+/+) or Snap25 (-/-) explants behaved in an identical fashion in P0-P3 Snap25 (+/+) cortical explants after 7 days in vitro. Thalamic projections from Snap25 (-/-) explants developed similar patterns of fibre ingrowth to the cortex, and stopped and formed branches at a similar depth in the Snap25(+/+) cortical slice as in control cultures. These results imply that thalamic projections can reach their ultimate target cells in layer 4, stop, and start to develop branches in the absence of regulated vesicular transmitter release from their own terminals.

摘要

我们对受调控囊泡释放介导的神经活动在皮层丘脑投射的停止和早期分支中的作用感兴趣。在 Snap25(-/-) 缺失突变体小鼠中,没有调控释放的情况下,轴突生长、到达皮层基板、等待期的侧支形成以及胚胎丘脑皮质投射的皮质板神经支配,并没有出现主要异常[Washbourne 等人(2002 年)《自然神经科学》5:19-26;Molnár 等人(2002 年)《神经科学杂志》10313-10323]。由于 Snap25(-/-) 缺失突变体小鼠在出生时死亡,我们之前的实验仅限于产前阶段。因此,我们通过使用异时性丘脑[胚胎日(E)16-E18]和皮质[生后日(P)0-P3]外植体的共培养模型,研究了丘脑投射的行为,以前已经证明了这种模型中的停止和分支行为。我们目前的共培养实验表明,来自 E16-E18 Snap25(+/+)或 Snap25(-/-)外植体的丘脑投射在体外 7 天后,在 P0-P3 Snap25(+/+)皮质外植体中以相同的方式表现。来自 Snap25(-/-)外植体的丘脑投射发育出与皮质相似的纤维内生长模式,并在 Snap25(+/+)皮质切片中以与对照培养物相似的深度停止并形成分支。这些结果表明,在没有来自其自身末端的受调控囊泡递质释放的情况下,丘脑投射可以到达其最终靶细胞层 4 并停止,并开始分支。

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