Gavaldà Núria, Pérez-Navarro Esther, Gratacòs Elena, Comella Joan X, Alberch Jordi
Departament de Biologia Cel.lular i Anatomia Patològica, Facultat de Medicina, Universitat de Barcelona, IDIBAPS, 08036 Barcelona, Spain.
Mol Cell Neurosci. 2004 Mar;25(3):460-8. doi: 10.1016/j.mcn.2003.11.012.
Brain-derived neurotrophic factor (BDNF) is a potent trophic factor for striatal cells that promotes survival and/or differentiation of GABAergic neurons in vitro. In the present study, we show that the stimulation of cultured striatal cells with BDNF increased the phosphorylation of Akt and p42/p44. This effect was specifically blocked by inhibitors of phosphatidylinositol 3-kinase (PI3-K) pathways (LY294002 and wortmannin) or p42/p44 mitogen-activated protein (MAP) kinase (PD98059 and U0126). BDNF treatment induced an increase in the number of calbindin-positive neurons but not in the number of GABAergic or total cells. Furthermore, BDNF increased the degree of dendritic arborization, soma area and axon length of striatal neurons. However, PD98059 was more effective blocking BDNF effects on calbindin- than on GABA-positive neurons, whereas LY294002 inhibited morphological differentiation in both neuronal populations. Moreover, BDNF induced neuronal survival only through the activation of the PI3-K pathway.
脑源性神经营养因子(BDNF)是一种对纹状体细胞具有强大作用的营养因子,在体外可促进γ-氨基丁酸能(GABAergic)神经元的存活和/或分化。在本研究中,我们发现用BDNF刺激培养的纹状体细胞可增加Akt和p42/p44的磷酸化。磷脂酰肌醇3激酶(PI3-K)途径抑制剂(LY294002和渥曼青霉素)或p42/p44丝裂原活化蛋白(MAP)激酶抑制剂(PD98059和U0126)可特异性阻断这一效应。BDNF处理可使钙结合蛋白阳性神经元数量增加,但不会使GABAergic神经元或总细胞数量增加。此外,BDNF可增加纹状体神经元的树突分支程度、胞体面积和轴突长度。然而,PD98059在阻断BDNF对钙结合蛋白阳性神经元的作用方面比阻断对GABA阳性神经元的作用更有效,而LY294002可抑制这两种神经元群体的形态分化。此外,BDNF仅通过激活PI3-K途径诱导神经元存活。