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去甲肾上腺素诱导的细胞内钙增加与星形胶质细胞大电导钙激活钾通道激活及毛细血管反应相关联。

Norepinephrine-induced intracellular Ca increase is coupled with astrocytic BK channel activation and capillary response.

作者信息

Bogdanović Pristov Jelena, Bataveljić Danijela, Bijelić Dunja, Milićević Katarina, Korać Jačić Jelena, Nikolić Ljiljana

机构信息

Department of Life Sciences, Institute for Multidisciplinary Research, University of Belgrade, Belgrade, Republic of Serbia.

Center for Laser Microscopy, Institute of Physiology and Biochemistry "Jean Giaja", Faculty of Biology, University of Belgrade, Belgrade, Republic of Serbia.

出版信息

Am J Physiol Cell Physiol. 2025 Oct 1;329(4):C1061-C1074. doi: 10.1152/ajpcell.00538.2025. Epub 2025 Aug 25.

Abstract

Astrocytes are abundant glial cells organized in a meshwork in which each cell is in contact with both neuronal and vascular elements. They receive and respond to neuronal signals and modulate synaptic activity and diameter of blood vessels through changes in their intracellular Ca. Norepinephrine plays an important role in both of these astrocytic functions; however, it remains unclear whether norepinephrine-induced intracellular Ca increase leads to further cellular adjustments in astrocyte activity. Here, we reveal a causal relationship between norepinephrine-induced intracellular Ca increase, α1-adrenergic receptor activation and activation of large-conductance Ca-dependent potassium ion (BK) channel in cultured rat cortical astrocytes. BK channel activation was abolished by α1-adrenergic receptor blockade, depletion of intracellular Ca stores, or dialysis of astrocytes with a Ca chelator. We further show that this norepinephrine-induced astrocytic Ca-BK channel coupling contributes to a reduction in cortical capillary diameter. The capillary response was prevented by pharmacological silencing of astrocytes or BK channel blockade, whereas the norepinephrine effect was mimicked by direct BK channel activation with an agonist in acute brain slices. In summary, these results elucidate a previously unrecognized cellular response of astrocytes to norepinephrine that is coupled with modulation of capillary diameter and may represent an integral part of the astrocytic communication with neurons and blood vessels. This study reveals adjustments of astrocyte activity in response to neurotransmitter norepinephrine. We provide compelling demonstration that norepinephrine-induced intracellular Ca increase is coupled with BK channel activation in cultured cortical astrocytes. Our results further indicate that norepinephrine-induced astrocytic Ca-BK channel signaling participates in modulation of capillary diameter in the cortex. These findings provide better understanding of astrocyte communication with neurons and blood vessels.

摘要

星形胶质细胞是丰富的神经胶质细胞,它们相互连接形成网络,每个细胞都与神经元和血管成分接触。它们接收并响应神经元信号,并通过细胞内钙离子的变化来调节突触活动和血管直径。去甲肾上腺素在这两种星形胶质细胞功能中都起着重要作用;然而,尚不清楚去甲肾上腺素诱导的细胞内钙离子增加是否会导致星形胶质细胞活性的进一步细胞调节。在这里,我们揭示了在培养的大鼠皮质星形胶质细胞中,去甲肾上腺素诱导的细胞内钙离子增加、α1-肾上腺素能受体激活与大电导钙依赖性钾离子(BK)通道激活之间的因果关系。α1-肾上腺素能受体阻断、细胞内钙库耗竭或用钙螯合剂对星形胶质细胞进行透析可消除BK通道的激活。我们进一步表明,这种去甲肾上腺素诱导的星形胶质细胞钙-BK通道偶联有助于皮质毛细血管直径的减小。通过药理学方法使星形胶质细胞沉默或阻断BK通道可防止毛细血管反应,而在急性脑片中用激动剂直接激活BK通道可模拟去甲肾上腺素的作用。总之,这些结果阐明了星形胶质细胞对去甲肾上腺素的一种先前未被认识的细胞反应,这种反应与毛细血管直径的调节相关,可能代表了星形胶质细胞与神经元和血管之间通讯的一个组成部分。这项研究揭示了星形胶质细胞对神经递质去甲肾上腺素的活性调节。我们提供了令人信服的证据,证明在培养的皮质星形胶质细胞中,去甲肾上腺素诱导的细胞内钙离子增加与BK通道激活相关。我们的结果进一步表明,去甲肾上腺素诱导的星形胶质细胞钙-BK通道信号参与了皮质毛细血管直径的调节。这些发现有助于更好地理解星形胶质细胞与神经元和血管之间的通讯。

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