Tsao D D, Wang S G, Lynn B D, Nagy J I
Department of Physiology and Pathophysiology, Faculty of Medicine, University of Manitoba, 745 Bannatyne Ave, Winnipeg, MB, R3E 0J9, Canada.
Eur J Neurosci. 2017 Jun;45(12):1553-1569. doi: 10.1111/ejn.13578. Epub 2017 May 11.
Gap junctions between cells in the pineal gland have been described ultrastructurally, but their connexin constituents have not been fully characterized. We used immunofluorescence in combination with markers of pineal cells to document the cellular localization of connexin43 (Cx43). Immunofluorescence labelling of Cx43 with several different antibodies was widely distributed throughout the pineal, whereas another connexin examined, connexin26, was not found in pineal but only in surrounding leptomeninges. Labelling apparently associated with plasma membranes was visualized either as fine Cx43-puncta (1-2 μm) or as unusually large pools of Cx43 ranging up to 4-7 μm in diameter or length. These puncta and pools were highly concentrated in perivascular spaces, where they were associated with numerous cells devoid of labelling for markers of pinealocytes (e.g. tryptophan hydroxylase and serotonin), and where they were minimally associated with blood vessels and lacked association with resident macrophages. Astrocytes labelled for glial fibrillary acidic protein were largely restricted to the anterior pole of the pineal gland, where they displayed only fine and sparse Cx43-puncta along their processes. Labelling for Cx43 was localized largely though not exclusively to the somata and long processes of a subpopulation of perivascular interstitial cells that were immunopositive for calbindin-D28K. These cells were often located among dense bundles or termination areas of sympathetic fibres labelled for tyrosine hydroxylase or serotonin. The results indicate that interstitial cells form abundant gap junctions composed of Cx43, and suggest that gap junction-mediated intracellular communication by these cells supports the activities of pinealocytes.
松果体中细胞间的缝隙连接已通过超微结构进行了描述,但其连接蛋白成分尚未完全明确。我们结合松果体细胞的标志物,利用免疫荧光技术来确定连接蛋白43(Cx43)的细胞定位。用几种不同抗体对Cx43进行免疫荧光标记,结果显示其在整个松果体中广泛分布,而另一种检测的连接蛋白连接蛋白26,未在松果体中发现,仅在周围的软脑膜中存在。明显与质膜相关的标记物,呈现为细小的Cx43斑点(1 - 2μm)或直径或长度达4 - 7μm的异常大的Cx43聚集区。这些斑点和聚集区高度集中在血管周围间隙,在那里它们与许多缺乏松果体细胞标志物(如色氨酸羟化酶和5-羟色胺)标记的细胞相关,并且在那里它们与血管的关联极小,也与常驻巨噬细胞无关。用胶质纤维酸性蛋白标记的星形胶质细胞主要局限于松果体的前极,在其突起上仅显示细小且稀疏的Cx43斑点。Cx43的标记主要(但并非完全)定位于血管周围间质细胞亚群的胞体和长突起上,这些细胞对钙结合蛋白-D28K呈免疫阳性。这些细胞常常位于标记酪氨酸羟化酶或5-羟色胺的交感神经纤维的致密束或终末区域之间。结果表明,间质细胞形成了由Cx43组成的丰富缝隙连接,并提示这些细胞通过缝隙连接介导的细胞内通讯支持松果体细胞的活动。