Structural and Intermolecular Associations Between Connexin36 and Protein Components of the Adherens Junction-Neuronal Gap Junction Complex

被引:12
|
作者
Nagy, J. I. [1 ]
Lynn, B. D. [1 ]
机构
[1] Univ Manitoba, Rady Fac Hlth Sci, Dept Physiol & Pathophysiol, Max Rady Coll Med, 745 Bannatyne Ave, Winnipeg, MB R3E 0J9, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
electrical synapses; electrical coupling; cell-cell adhesion; intracellular signaling; mesencephalic trigeminal nucleus; immunofluorescence; CELL-ADHESION MOLECULES; MAIN OLFACTORY-BULB; ELECTRICAL SYNAPSES; ZONULA OCCLUDENS-1; BINDING PROTEIN; NMDA RECEPTOR; SPINAL-CORD; PDZ DOMAIN; MESENCEPHALIC NUCLEUS; EPITHELIAL-CELLS;
D O I
10.1016/j.neuroscience.2018.05.026
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Intimate structural and functional relationships between gap junctions and adherens junctions have been demonstrated in peripheral tissues, but have not been thoroughly examined in the central nervous system, where adherens junctions are often found in close proximity to neuronal gap junctions. Here, we used immunofluorescence approaches to document the localization of various protein components of adherens junctions in relation to those that we have previously reported to occur at electrical synapses formed by neuronal gap junctions composed of connexin36 (Cx36). The adherens junction constituents N-cadherin and nectin-1 were frequently found to localize near or overlap with Cx36-containing gap junctions in several brain regions examined. This was also true of the adherens junction-associated proteins alpha-catenin and beta-catenin, as well as the proteins zonula occludens-1 and AF6 (aka, afadin) that were reported constituents of both adherens junctions and gap junctions. The deployment of the protein constituents of these junctions was especially striking at somatic contacts between primary afferent neurons in the mesencephalic trigeminal nucleus (MesV), where the structural components of adherens junctions appeared to be maintained in connexin36 null mice. These results support emerging views concerning the multi-molecular composition of electrical synapses and raise possibilities for various structural and functional protein-protein interactions at what now can be considered the adherens junction-neuronal gap junction complex. Further, the results point to intracellular signaling pathways that could potentially contribute to the assembly, maintenance and turnover of this complex, as well as to the dynamic nature of neuronal communication at electrical synapses. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:241 / 261
页数:21
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