Dobrenis K, Chang H-Y, Pina-Benabou M H, Woodroffe A, Lee S C, Rozental R, Spray D C, Scemes E
Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
J Neurosci Res. 2005 Nov 1;82(3):306-15. doi: 10.1002/jnr.20650.
Microglia, the tissue macrophages of the central nervous system (CNS), intimately interact with neurons physically and through soluble factors that can affect microglial activation state and neuronal survival and physiology. We report here a new mechanism of interaction between these cells, provided by the formation of gap junctions composed of connexin (Cx) 36. Among eight Cxs tested, expression of Cx36 mRNA and protein was found in microglial cultures prepared from human and mouse, and Cx45 mRNA was found in mouse microglial cultures. Electrophysiological measurements found coupling between one-third of human or mouse microglial pairs that averaged below 30 pico-Siemens and displayed electrical properties consistent with Cx36 gap junctions. Importantly, similar frequency of low-strength electrical coupling was also obtained between microglia and neurons in cocultures prepared from neocortical or hippocampal rodent tissue. Lucifer yellow dye coupling between neurons and microglia was observed in 4% of pairs tested, consistent with the low strength and incidence of electrical coupling. Cx36 expression level and/or the degree of coupling between microglia did not significantly change in the presence of activating agents, including lipopolysaccharide, granulocyte-macrophage colony-stimulating factor, interferon-gamma, and tumor necrosis factor-alpha, except for some reduction of Cx36 protein when exposed to the latter two agents. Our findings that intercellular coupling occurs between neuronal and microglial populations through Cx36 gap junctions have potentially important implications for normal neural physiology and microglial responses in neuronopathology in the mammalian CNS.
小胶质细胞是中枢神经系统(CNS)的组织巨噬细胞,通过与神经元的直接接触以及可影响小胶质细胞激活状态、神经元存活和生理功能的可溶性因子,与神经元密切相互作用。我们在此报告了这些细胞之间一种新的相互作用机制,即由连接蛋白(Cx)36组成的缝隙连接的形成。在测试的8种连接蛋白中,在人和小鼠制备的小胶质细胞培养物中发现了Cx36 mRNA和蛋白的表达,在小鼠小胶质细胞培养物中发现了Cx45 mRNA。电生理测量发现,三分之一的人或小鼠小胶质细胞对之间存在耦合,平均耦合低于30皮西门子,并且显示出与Cx36缝隙连接一致的电学特性。重要的是,在由新皮质或海马啮齿动物组织制备的共培养物中,小胶质细胞与神经元之间也获得了相似频率的低强度电耦合。在4%的测试细胞对中观察到了神经元与小胶质细胞之间的荧光黄染料耦合,这与电耦合的低强度和发生率一致。除了暴露于后两种因子时Cx36蛋白略有减少外,在包括脂多糖、粒细胞-巨噬细胞集落刺激因子、干扰素-γ和肿瘤坏死因子-α在内的激活剂存在下,小胶质细胞之间的Cx36表达水平和/或耦合程度没有显著变化。我们的研究结果表明,神经元和小胶质细胞群体之间通过Cx36缝隙连接发生细胞间耦合,这对哺乳动物中枢神经系统的正常神经生理学和神经病理学中的小胶质细胞反应可能具有重要意义。