Mizoguchi Yoshito, Nabekura Junichi
Cellular and Systems Physiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka 812-8582, Japan.
Neuroreport. 2003 Aug 6;14(11):1481-3. doi: 10.1097/00001756-200308060-00015.
A 1-2 min application of brain-derived neurotrophic factor (BDNF; 20 ng/ml) induced sustained elevation of intracellular Ca2+ lasting > 90 min, using the fura-2 imaging of intracellular Ca2+ mobilization, in visual cortical pyramidal neurons isolated from rats. BDNF increased intracellular Ca2+ through the PLC-gamma phosphorylation after the TrkB receptor tyrosine kinase activation. Either K252a or U73122 suppressed intracellular Ca2+ in the absence of BDNF. We suggest that sustained activation of Trk B receptor tyrosine kinase and PLC-gamma occurs after a brief BDNF application and contributes to the short-term maintenance (< 30 min) of the sustained intracellular Ca2+ elevation.
利用fura-2成像技术对细胞内Ca2+动员进行检测,结果显示,在从大鼠分离出的视皮层锥体神经元中,应用脑源性神经营养因子(BDNF;20 ng/ml)1 - 2分钟,可诱导细胞内Ca2+持续升高,持续时间超过90分钟。BDNF通过激活TrkB受体酪氨酸激酶后使PLC-γ磷酸化,从而增加细胞内Ca2+。在没有BDNF的情况下,K252a或U73122均可抑制细胞内Ca2+。我们认为,短暂应用BDNF后会发生Trk B受体酪氨酸激酶和PLC-γ的持续激活,这有助于细胞内Ca2+持续升高的短期维持(< 30分钟)。