Dept. of Environmental and Occupational Health Sciences, University of Washington, Seattle, WA 98105, USA.
Eur J Pharmacol. 2011 Jun 1;659(2-3):102-7. doi: 10.1016/j.ejphar.2011.03.019. Epub 2011 Mar 29.
Astrocytes have been shown to release factors that affect various aspects of neuronal development. We have previously shown that the acetylcholine analog carbachol, by activating muscarinic M(3) receptors in rat astrocytes, increases their ability to promote neuritogenesis in hippocampal neurons. This effect was mediated by an increased expression and release by astrocytes of several permissive factors, a most relevant of which was fibronectin. In the present study we investigated the signal transduction pathways involved in these effects of carbachol in astrocytes. Results show that multiple pathways are involved in the effects of carbachol on astrocyte-mediated increases in fibronectin expression and neuritogenesis. These include the phospholipase D pathway, leading to sequential activation of protein kinase C (PKC) ζ, p70S6 kinase and nuclear factor-κB; the phosphoinositide-3 kinase pathway; and the PKC ε pathway leading to activation of mitogen activated protein kinase. These pathways were shown to mediate the effect of carbachol on neurite outgrowth as well as the increased expression of fibronectin, further substantiating the important role of the latter in astrocyte-mediated neuritogenesis. Interference with these signaling pathways would be expected to impair astrocyte-neurons communication leading to impaired neuronal development.
星形胶质细胞已被证明可以释放影响神经元发育各个方面的因子。我们之前曾表明,乙酰胆碱类似物卡巴胆碱通过激活大鼠星形胶质细胞中的毒蕈碱 M3 受体,增加其促进海马神经元神经突生成的能力。这种效应是通过星形胶质细胞表达和释放几种允许因子来介导的,其中最相关的是纤维连接蛋白。在本研究中,我们研究了卡巴胆碱在星形胶质细胞中引起这些效应的信号转导途径。结果表明,多种途径参与了卡巴胆碱对星形胶质细胞介导的纤维连接蛋白表达和神经突生成增加的影响。这些途径包括磷脂酶 D 途径,导致蛋白激酶 C(PKC)ζ、p70S6 激酶和核因子-κB 的顺序激活;磷酸肌醇-3 激酶途径;以及 PKCε 途径,导致丝裂原活化蛋白激酶的激活。这些途径介导了卡巴胆碱对神经突生长和纤维连接蛋白表达增加的影响,进一步证实了后者在星形胶质细胞介导的神经突生成中的重要作用。干扰这些信号通路预计会损害星形胶质细胞-神经元通讯,导致神经元发育受损。