Speggiorin Michele, Chiavegato Angela, Zonta Micaela, Gómez-Gonzalo Marta
Department of Biomedical Sciences, Università degli Studi di Padova, 35131 Padova, Italy.
Neuroscience Institute, Section of Padova, National Research Council (CNR), 35131 Padova, Italy.
Cells. 2024 Dec 30;14(1):24. doi: 10.3390/cells14010024.
Astrocytes from different brain regions respond with Ca elevations to the catecholamine norepinephrine (NE). However, whether this noradrenergic-mediated signaling is present in astrocytes from the ventral tegmental area (VTA), a dopaminergic circuit receiving noradrenergic inputs, has not yet been investigated. To fill in this gap, we applied a pharmacological approach along with two-photon microscopy and an AAV strategy to express a genetically encoded calcium indicator in VTA astrocytes. We found that VTA astrocytes from both female and male young adult mice showed a strong Ca response to NE at both soma and processes. Our results revealed that Gq-coupled α1 adrenergic receptors, which elicit the production of IP3, are the main mediators of the astrocyte response. In mice lacking the IP3 receptor type-2 (IP3R2 mice), we found that the astrocyte response to NE, even if reduced, is still present. We also found that in IP3R2 astrocytes, the residual Ca elevations elicited by NE depend on the release of Ca from the endoplasmic reticulum, through IP3Rs different from IP3R2. In conclusion, our results reveal VTA astrocytes as novel targets of the noradrenergic signaling, opening to new interpretations of the cellular and molecular mechanisms that mediate the NE effects in the VTA.
来自不同脑区的星形胶质细胞会通过钙离子浓度升高来响应儿茶酚胺去甲肾上腺素(NE)。然而,在腹侧被盖区(VTA)的星形胶质细胞中,这种去甲肾上腺素能介导的信号传导是否存在尚未得到研究,VTA是一个接受去甲肾上腺素能输入的多巴胺能回路。为了填补这一空白,我们采用了药理学方法,结合双光子显微镜和腺相关病毒(AAV)策略,在VTA星形胶质细胞中表达一种基因编码的钙指示剂。我们发现,来自雌性和雄性成年小鼠的VTA星形胶质细胞在胞体和突起处对NE均表现出强烈的钙离子反应。我们的结果表明,引发三磷酸肌醇(IP3)产生的Gq偶联α1肾上腺素能受体是星形胶质细胞反应的主要介质。在缺乏2型IP3受体的小鼠(IP3R2小鼠)中,我们发现星形胶质细胞对NE的反应即使减弱仍存在。我们还发现,在IP3R2星形胶质细胞中,NE引发的残余钙离子浓度升高依赖于通过不同于IP3R2的IP3受体从内质网释放钙离子。总之,我们的结果揭示了VTA星形胶质细胞是去甲肾上腺素能信号传导的新靶点,为介导NE在VTA中作用的细胞和分子机制开辟了新的解释途径。