Jeanson Tiffany, Pondaven Audrey, Ezan Pascal, Mouthon Franck, Charvériat Mathieu, Giaume Christian
Collège de France, Center for Interdisciplinary Research in Biology/Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7241/Institut National de la Santé et de la Recherche Médicale U1050Paris, France; University Pierre et Marie CurieParis, France; MemoLife Laboratory of Excellence and Paris Science Lettre Research UniversityParis, France; TheranexusLyon, France.
Collège de France, Center for Interdisciplinary Research in Biology/Centre National de la Recherche Scientifique, Unité Mixte de Recherche 7241/Institut National de la Santé et de la Recherche Médicale U1050Paris, France; University Pierre et Marie CurieParis, France; MemoLife Laboratory of Excellence and Paris Science Lettre Research UniversityParis, France.
Front Cell Neurosci. 2016 Jan 7;9:495. doi: 10.3389/fncel.2015.00495. eCollection 2015.
Glial cells, and in particular astrocytes, are crucial to maintain neuronal microenvironment by regulating energy metabolism, neurotransmitter uptake, gliotransmission, and synaptic development. Moreover, a typical feature of astrocytes is their high expression level of connexins, a family of membrane proteins that form gap junction channels allowing intercellular exchanges and hemichannels that provide release and uptake pathways for neuroactive molecules. Interestingly, several studies have revealed unexpected changes in astrocytes from depressive patients and rodent models of depressive-like behavior. Moreover, changes in the expression level of the astroglial connexin 43 (Cx43) have been reported in a depressive context. On the other hand, antidepressive drugs have also been shown to impact the expression of this connexin in astrocytes. However, so far there is little information concerning the functional consequence of these changes, i.e., the status of gap junctional communication and hemichannel activity in astrocytes exposed to antidepressants. In the present work we focused our attention on the action of seven antidepressants from four different therapeutic classes and tested their effects on Cx43 expression and on the two connexin-based channels functions studied in cultured astrocytes. We here report that when used at non-toxic and clinically relevant concentrations they have no effects on Cx43 expression but differential effects on Cx43 gap junction channels. Moreover, all tested antidepressants inhibit Cx43 hemichannel with different efficiency depending on their therapeutic classe. By studying the impact of antidepressants on the functional status of astroglial connexin channels, contributing to dynamic neuroglial interactions, our observations should help to better understand the mechanism by which these drugs provide their effect in the brain.
神经胶质细胞,尤其是星形胶质细胞,对于通过调节能量代谢、神经递质摄取、胶质传递和突触发育来维持神经元微环境至关重要。此外,星形胶质细胞的一个典型特征是它们高表达连接蛋白,这是一类膜蛋白,可形成允许细胞间交换的缝隙连接通道以及为神经活性分子提供释放和摄取途径的半通道。有趣的是,多项研究揭示了抑郁症患者和抑郁样行为啮齿动物模型中星形胶质细胞的意外变化。此外,在抑郁背景下,已报道星形胶质细胞连接蛋白43(Cx43)的表达水平发生变化。另一方面,抗抑郁药物也已被证明会影响星形胶质细胞中这种连接蛋白的表达。然而,到目前为止,关于这些变化的功能后果,即暴露于抗抑郁药物的星形胶质细胞中缝隙连接通讯和半通道活性的状态,几乎没有相关信息。在本研究中,我们将注意力集中在来自四种不同治疗类别的七种抗抑郁药物的作用上,并测试了它们对Cx43表达以及在培养的星形胶质细胞中研究的两种基于连接蛋白的通道功能的影响。我们在此报告,当以无毒且与临床相关的浓度使用时,它们对Cx43表达没有影响,但对Cx43缝隙连接通道有不同的影响。此外,所有测试的抗抑郁药物均以不同效率抑制Cx43半通道,这取决于它们的治疗类别。通过研究抗抑郁药物对星形胶质细胞连接蛋白通道功能状态的影响,这有助于动态的神经胶质细胞相互作用,我们的观察结果应有助于更好地理解这些药物在大脑中发挥作用的机制。