Nakajima K, Kikuchi Y, Ikoma E, Honda S, Ishikawa M, Liu Y, Kohsaka S
Department of Neurochemistry, National Institute of Neuroscience, Kodaira, Tokyo, Japan.
Glia. 1998 Nov;24(3):272-89. doi: 10.1002/(sici)1098-1136(199811)24:3<272::aid-glia2>3.0.co;2-4.
Although the physiological role of neurotrophins in neuronal development and survival has been extensively investigated, their role in glial cell physiology remains to be elucidated. In the present study, we investigated the effects of neurotrophins on cultured microglia from newborn rat brain. All of the neurotrophins tested nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), neurotrophin-3 (NT-3), and neurotrophin-4 (NT-4), increased the secretion of plasminogen and urokinase type-plasminogen activator and specific activity of acid phosphatase, but suppressed the release of constitutively-produced and lipopolysaccharide-stimulated nitric oxide (NO) from microglia. The reverse transcription-polymerase chain reaction, immunocytochemical staining, and Western blotting revealed that cultured microglia express Trk A, B, and C, and low-affinity NGF receptor, LNGFRp75. Neurotrophin was found to phosphorylate Trk A and B, and the neurotrophin-induced enhancement of plasminogen-secretion was suppressed by protein kinase inhibitor, K252a. Furthermore, neurotrophins caused an activation of transcription factor, NF-kappaB. These results indicate that the neurotrophin family regulate the function of microglia through Trk and/or LNGFRp75-mediated signal transduction.
尽管神经营养因子在神经元发育和存活中的生理作用已得到广泛研究,但其在神经胶质细胞生理学中的作用仍有待阐明。在本研究中,我们研究了神经营养因子对新生大鼠脑培养小胶质细胞的影响。所测试的所有神经营养因子——神经生长因子(NGF)、脑源性神经营养因子(BDNF)、神经营养因子-3(NT-3)和神经营养因子-4(NT-4),均增加了纤溶酶原和尿激酶型纤溶酶原激活剂的分泌以及酸性磷酸酶的比活性,但抑制了小胶质细胞组成性产生的和脂多糖刺激的一氧化氮(NO)的释放。逆转录-聚合酶链反应、免疫细胞化学染色和蛋白质印迹显示,培养的小胶质细胞表达Trk A、B和C以及低亲和力NGF受体LNGFRp75。发现神经营养因子使Trk A和B磷酸化,并且神经营养因子诱导的纤溶酶原分泌增强被蛋白激酶抑制剂K252a抑制。此外,神经营养因子引起转录因子NF-κB的激活。这些结果表明,神经营养因子家族通过Trk和/或LNGFRp75介导的信号转导调节小胶质细胞的功能。