Wang Xiaojing, Zheng Honghua, Liu Changjin, Zhu Changgeng, Wang Wei, Li Zhengli
Department of Anatomy, Tongji Medical College, Huazhong University of Science and Technology, 13 Hangkong Rd, Wuhan, Hubei 430030, PR China.
Neurochem Res. 2008 May;33(5):826-32. doi: 10.1007/s11064-007-9514-7. Epub 2007 Oct 17.
Astrocytes are activated by ciliary neurotrophic factor (CNTF) in vivo and in vitro, however, the consequences on the L-type calcium channel (LCC) of neurons are still poorly understood. Therefore, in the present study, whole-cell patch clamp, western-blot and RT-PCR assay were performed to evaluate the effects of CNTF-treated astrocyte conditioned medium (CNTF-ACM) on LCC current (I(Ca)-L) and the expression of Cav1.2 and Cav1.3 in Sprague-Dawley rat cortical neurons. The results revealed that CNTF-ACM enhanced the amplitude of Ica-L and the expression of Cav1.3 significantly, but had no effects on Cav1.2 expression. We also found an increase in the concentration of fibroblast growth factor-2 (FGF-2) in CNTF-ACM by ELISA assay. Taken together, these findings indicate that CNTF induces the release of factors, including FGF-2, from astrocytes, thereby potentiating the activity of LCC in cortical neurons.
在体内和体外,睫状神经营养因子(CNTF)均可激活星形胶质细胞,然而,其对神经元L型钙通道(LCC)的影响仍知之甚少。因此,在本研究中,采用全细胞膜片钳、蛋白质免疫印迹和逆转录聚合酶链反应分析,以评估经CNTF处理的星形胶质细胞条件培养基(CNTF-ACM)对Sprague-Dawley大鼠皮层神经元LCC电流(I(Ca)-L)以及Cav1.2和Cav1.3表达的影响。结果显示,CNTF-ACM显著增强了Ica-L的幅度以及Cav1.3的表达,但对Cav1.2的表达无影响。通过酶联免疫吸附测定法,我们还发现CNTF-ACM中成纤维细胞生长因子-2(FGF-2)的浓度有所增加。综上所述,这些发现表明,CNTF可诱导星形胶质细胞释放包括FGF-2在内的因子,从而增强皮层神经元中LCC的活性。