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大鼠海马器官型脑片培养中锥体神经元胞质钙的光学成像、电生理学及超微结构研究

Optical imaging of cytosolic calcium, electrophysiology, and ultrastructure in pyramidal neurons of organotypic slice cultures from rat hippocampus.

作者信息

Pozzo Miller L D, Petrozzino J J, Mahanty N K, Connor J A

机构信息

Roche Institute of Molecular Biology, Roche Research Center, Nutley, New Jersey 07110-1199, USA.

出版信息

Neuroimage. 1993 Sep;1(2):109-20. doi: 10.1006/nimg.1993.1004.

Abstract

Organotypic slice cultures from rat hippocampal cortex grown in an interface between culture medium and a CO2-enriched atmosphere maintained much of the morphological connectivity characteristic of the hippocampus in situ and thinned out considerably, facilitating optical measurements of fluorescent dyes sensitive to Ca2+ in individual neurons. Pyramidal neurons of the CA3 region presented morphological features of differentiated cells, including complex dendritic arborization and large numbers of dendritic spines. The fine cytoskeletal substructure at the postsynaptic density, below the plasma membrane, and within the core of the head and neck of dendritic spines in rapidly frozen slice cultures presents the characteristic morphology previously described for Purkinje cell dendritic spines in acutely dissected cerebellar cortex slices after rapid freezing. CA3 neurons responded to intracellular current injection with a train of action potentials, spike frequency adaptation, and a slow afterhyperpolarization. These spike trains caused rapid increases in dendritic [Ca2+]i that decayed to resting levels after termination of the current pulse. Dendritic spines were clearly observed in proximal dendrites of CA3 neurons in live preparations. [Ca2+]i transients in these dendritic spines closely followed the changes observed in the main dendritic shaft. Orthodromic synaptic stimulation from the dentate hilus generated long-lasting synaptic potentials accompanied by large [Ca2+]i transient in CA3 pyramidal neurons. The [Ca2+]i response was first observed in the proximal dendrites, after which the soma exhibited a [Ca2+]i increase, returning to resting levels within 10 s after the synaptic stimulus. Slice cultures thus provide a favorable opportunity to investigate [Ca2+]i responses in individual neurons maintained in an organotypic synaptic environment, taking advantage of high-resolution optical techniques.

摘要

在培养基与富含二氧化碳的气氛之间的界面中生长的大鼠海马皮质器官型切片培养物,保留了海马原位许多形态学连接特征,并且显著变薄,便于对单个神经元中对Ca2+敏感的荧光染料进行光学测量。CA3区的锥体神经元呈现出分化细胞的形态学特征,包括复杂的树突分支和大量的树突棘。在快速冷冻的切片培养物中,突触后密度、质膜下方以及树突棘头部和颈部核心内的精细细胞骨架亚结构呈现出先前在快速冷冻后急性解剖的小脑皮质切片中浦肯野细胞树突棘所描述的特征形态。CA3神经元对细胞内电流注入产生一系列动作电位、动作电位频率适应和缓慢的超极化后电位。这些动作电位序列导致树突[Ca2+]i迅速增加,在电流脉冲终止后衰减至静息水平。在活体制备中,在CA3神经元的近端树突中清晰地观察到树突棘。这些树突棘中的[Ca2+]i瞬变紧密跟随在主要树突干中观察到的变化。来自齿状回门区的顺向突触刺激在CA3锥体神经元中产生持久的突触电位,并伴有大的[Ca2+]i瞬变。[Ca2+]i反应首先在近端树突中观察到,之后胞体表现出[Ca2+]i增加,在突触刺激后10秒内恢复到静息水平。因此,切片培养物提供了一个有利的机会,利用高分辨率光学技术研究在器官型突触环境中单个神经元的[Ca2+]i反应。

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