Hartikka J, Hefti F
Department of Neurology, University of Miami School of Medicine, Florida 33101.
J Neurosci. 1988 Aug;8(8):2967-85. doi: 10.1523/JNEUROSCI.08-08-02967.1988.
To characterize the role of NGF in the development of forebrain cholinergic neurons, we established primary cell culture systems to grow these cells under controlled in vitro conditions. Cultures of dissociated cells were prepared from the septal area of fetal (E17) rats, which contained part of the group of basal forebrain cholinergic neurons. Cultures were treated either with NGF (100 ng/ml) or with an antiserum against NGF (1:500 dilution). To assess the influence of non-neuronal cells, 2 types of high-density cultures were prepared: mixed neuronal-glial cultures and pure neuronal cultures. Cholinergic neurons were identified using choline acetyltransferase (ChAT) immunocytochemistry and AChE cytochemistry. Receptors for NGF (NGF-R) were located immunocytochemically using monoclonal antibodies against rat NGF-R. We report that, first, NGF-R are exclusively localized on cholinergic neurons in septal cultures. All neurons labeled with antibodies against NGF-R also contained AChE. Twenty-one percent of all AChE-positive neurons were not stained in NGF-R immunocytochemistry (AChE has earlier been shown to be colocalized with ChAT in septal cultures). Second, NGF treatment increases and anti-NGF treatment reduces the number of AChE-positive neurons in cultures of low plating density, suggesting that NGF promotes survival of septal cholinergic neurons in these cultures. In cultures of high plating density, NGF increased the number of NGF-R and ChAT-positive neurons without affecting the number of AChE-positive neurons in these cultures. These results suggest that exogenous NGF is not required for survival of cholinergic neurons in high-density cultures but stimulates the expression of ChAT and NGF-R. Third, NGF stimulates fiber growth of septal cholinergic neurons, as assessed by computerized image analysis of AChE-positive neurons. Fourth, NGF specifically increases ChAT and AChE activities in septal cultures. These NGF-mediated increases in enzyme activities are more pronounced when neurons are grown together with glial cells. In pure neuronal cultures, NGF increased ChAT and AChE activities by 101 and 16%, and in mixed neuronal-glial cultures by 318 and 87%, respectively. Anti-NGF blocked the effects of NGF but failed to reduce ChAT and AChE activities below control levels in cultures of high plating density. Fifth, astrocytes attenuate the expression of ChAT and AChE by septal neurons in the absence of NGF.(ABSTRACT TRUNCATED AT 400 WORDS)
为了描述神经生长因子(NGF)在前脑胆碱能神经元发育中的作用,我们建立了原代细胞培养系统,以便在可控的体外条件下培养这些细胞。从胎鼠(胚胎第17天,E17)的隔区制备解离细胞培养物,该区域包含一部分基底前脑胆碱能神经元群。培养物分别用NGF(100 ng/ml)或抗NGF抗血清(1:500稀释)处理。为了评估非神经元细胞的影响,制备了两种类型的高密度培养物:神经元-胶质混合培养物和纯神经元培养物。使用胆碱乙酰转移酶(ChAT)免疫细胞化学和乙酰胆碱酯酶(AChE)细胞化学鉴定胆碱能神经元。使用抗大鼠NGF受体(NGF-R)的单克隆抗体通过免疫细胞化学定位NGF受体。我们报告,首先,在隔区培养物中,NGF-R仅定位在胆碱能神经元上。所有用抗NGF-R抗体标记的神经元也含有AChE。在NGF-R免疫细胞化学中,所有AChE阳性神经元中有21%未被染色(先前已证明在隔区培养物中AChE与ChAT共定位)。其次,在低密度接种培养物中,NGF处理增加而抗NGF处理减少AChE阳性神经元的数量,这表明NGF促进这些培养物中隔区胆碱能神经元的存活。在高密度接种培养物中,NGF增加了NGF-R和ChAT阳性神经元的数量,但不影响这些培养物中AChE阳性神经元的数量。这些结果表明,在高密度培养物中,胆碱能神经元的存活不需要外源性NGF,但它刺激ChAT和NGF-R的表达。第三,通过对AChE阳性神经元的计算机图像分析评估,NGF刺激隔区胆碱能神经元的纤维生长。第四,NGF特异性增加隔区培养物中ChAT和AChE的活性。当神经元与胶质细胞一起生长时,这些由NGF介导的酶活性增加更为明显。在纯神经元培养物中,NGF使ChAT和AChE活性分别增加101%和16%,在神经元-胶质混合培养物中分别增加318%和87%。抗NGF阻断了NGF的作用,但未能使高密度接种培养物中的ChAT和AChE活性降低到对照水平以下。第五,在没有NGF的情况下,星形胶质细胞减弱隔区神经元中ChAT和AChE的表达。(摘要截短于第400个词)