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腹侧被盖区各亚区内多巴胺 D2 受体和树突体囊泡单胺转运体 2(VMAT2)的区域特异性靶向。

Region-specific targeting of dopamine D2-receptors and somatodendritic vesicular monoamine transporter 2 (VMAT2) within ventral tegmental area subdivisions.

作者信息

Pickel Virginia M, Chan June, Nirenberg Melissa J

机构信息

Department of Neurology and Neuroscience, Weill Medical College of Cornell University, New York, New York 10021, USA.

出版信息

Synapse. 2002 Aug;45(2):113-24. doi: 10.1002/syn.10092.

Abstract

Throughout the ventral tegmental area (VTA), dopamine is packaged within subcellular organelles by the vesicular monoamine transporter-2 (VMAT2). Somatodendritically released dopamine in this region binds to the D2 receptor (D2R) to modulate ongoing neurotransmission. Although autoregulation of mesocortical dopaminergic neurons in the parabrachial VTA (PB-VTA) is known to be less efficacious than that of mesolimbic dopaminergic neurons in the paranigral (PN-VTA), the cellular basis for this regional heterogeneity is not known. For this reason, we used electron microscopic immunocytochemistry to determine the subcellular localization of the dopamine storage vesicles (identified by the presence of VMAT2) in relation to the D2R in these VTA subdivisions. In both regions, D2R immunoreactivity was principally located on extrasynaptic dendritic plasma membranes near excitatory-type synapses. Equivalent percentages (72 and 74%) of the D2R-labeled dendrites in each region contained VMAT2-immunoreactive tubulovesicles. Of the total VMAT2-labeled dendrites, however, a significantly lower percentage in the PB-VTA (26%) than in the PN-VTA (38%) contained D2R labeling. In contrast, a significantly higher number of VMAT2 immunogold-silver deposits was seen within individual dendrites in the PB-VTA than in PN-VTA. In both regions, D2R immunoreactivity was also detected in VMAT2-negative axon terminals that formed synapses on dendrites containing VMAT2. Our results are the first to demonstrate that within VTA neurons and their afferents the D2R is strategically positioned for activation by dopamine released from dendritic storage vesicles. These findings also suggest that the potential for D2R activation may affect the expression levels of VMAT2 in VTA dendrites.

摘要

在整个腹侧被盖区(VTA),多巴胺由囊泡单胺转运体2(VMAT2)包装在亚细胞器内。该区域树突体释放的多巴胺与D2受体(D2R)结合,以调节正在进行的神经传递。虽然已知臂旁VTA(PB-VTA)中中皮质多巴胺能神经元的自身调节比黑质旁(PN-VTA)中中脑边缘多巴胺能神经元的自身调节效率低,但其区域异质性的细胞基础尚不清楚。因此,我们使用电子显微镜免疫细胞化学来确定多巴胺储存囊泡(通过VMAT2的存在来识别)相对于这些VTA亚区中D2R的亚细胞定位。在这两个区域中,D2R免疫反应性主要位于兴奋性突触附近的突触外树突质膜上。每个区域中72%和74%的D2R标记树突含有VMAT2免疫反应性微管小泡。然而,在PB-VTA中,VMAT2标记树突中含有D2R标记的比例(26%)显著低于PN-VTA(38%)。相反,在PB-VTA中,单个树突内可见的VMAT2免疫金银沉积物数量显著多于PN-VTA。在这两个区域中,在形成于含有VMAT2的树突上的突触的VMAT2阴性轴突终末中也检测到了D2R免疫反应性。我们的结果首次表明,在VTA神经元及其传入神经中,D2R处于战略位置,可被树突储存囊泡释放的多巴胺激活。这些发现还表明,D2R激活的可能性可能影响VTA树突中VMAT2的表达水平。

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