首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Dense core vesicles resemble active-zone transport vesicles and are diminished following synaptogenesis in mature hippocampal slices.
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Dense core vesicles resemble active-zone transport vesicles and are diminished following synaptogenesis in mature hippocampal slices.

机译:密集的核心囊泡类似于活性区转运囊泡,并且在成熟的海马切片中发生突触后减少。

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摘要

Large dense core vesicles (approximately 100 nm) contain neuroactive peptides and other co-transmitters. Smaller dense core vesicles (approximately 80 nm) are known to contain components of the presynaptic active zone and thought to transport and deliver these components during developmental synaptogenesis. It is not known whether excitatory axons in area CA1 contain such dense core vesicles, and whether they contribute to synaptic plasticity of mature hippocampus. Serial section electron microscopy was used to identify dense core vesicles in presynaptic axons in s. radiatum of area CA1 in adult rat hippocampus. Comparisons were made among perfusion-fixed hippocampus and hippocampal slices that undergo synaptogenesis during recovery in vitro. Dense core vesicles occurred in 26.1+/-3.6% of axonal boutons in perfusion fixed hippocampus, and in only 17.6+/-4.5% of axonal boutons in hippocampal slices (P<0.01). Most of the dense core vesicle positive boutons contained only one dense core vesicle, and no reconstructed axonal bouton had more than a total of 10 dense core vesicles in either condition. Overall the dense core vesicles had average diameters of 79+/-11 nm. These small dense core vesicles were usually located near nonsynaptic membranes and rarely occurred near the edge of a presynaptic active zone. Their size, low frequency, locations, and decrease following recuperative synaptogenesis in slices are novel findings that merit further study with respect to small dense core vesicle content and possible contributions to synapse assembly and plasticity in the mature hippocampus.
机译:大而密集的核心囊泡(约100 nm)包含神经活性肽和其他共递质。较小的致密核心囊泡(约80 nm)已知包含突触前活性区的成分,并被认为在发育性突触形成过程中运输和递送这些成分。尚不清楚CA1区的兴奋性轴突是否包含这种致密的核心囊泡,以及它们是否有助于成熟海马的突触可塑性。连续切片电子显微镜用于鉴定s中突触前轴突中的密集核心囊泡。成年大鼠海马区CA1区的辐射半径。比较了在灌注修复的海马体和在体外恢复过程中发生突触的海马体片之间。在固定的海马中,密集的核心囊泡出现在26.1 +/- 3.6%的轴突突中,而在海马切片中仅发生在17.6 +/- 4.5%的轴突突中(P <0.01)。大多数致密核心囊泡阳性囊仅包含一个致密核心囊泡,在任何一种情况下,没有重建的轴突囊囊具有总数超过10个的致密核心囊泡。总体上,致密的核心囊泡的平均直径为79 +/- 11nm。这些小的致密核心囊泡通常位于非突触膜附近,很少出现在突触前活性区边缘附近。他们的大小,低频,位置和减少片状调理突触后减少是新的发现,值得关于小密集核心囊泡含量以及可能对成熟的海马突触组装和可塑性做出贡献的进一步研究。

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