Hartikka J, Hefti F
Department of Neurobiology, University of Miami, FL 33101.
J Neurosci Res. 1988 Oct-Dec;21(2-4):352-64. doi: 10.1002/jnr.490210227.
In the central nervous system, nerve growth factor (NGF) affects basal forebrain cholinergic neurons during early development and in the adult mammalian brain. These neurons are located in medial septum, diagonal band of Broca, and nucleus basalis of Meynert. While the effects of NGF on the development of septal cholinergic neurons are well documented, only little is known about the influence of NGF on development of cholinergic neurons in the nucleus basalis. In addition to the basal forebrain cholinergic neurons, there are cholinergic interneurons in the corpus striatum, which form an anatomically and functionally distinct population of cholinergic neurons. These striatal interneurons have been reported to respond to NGF during early development; however, it is not known whether the effects of NGF on their development are similar to those on septal cholinergic neurons. We prepared cultures of dissociated cells from fetal rat septum, striatum, and nucleus basalis and investigated the development of cholinergic neurons localized in these three different areas in the presence or absence of NGF. We now report that, first, cholinergic neurons of striatum and nucleus basalis develop a more extensive fiber network and contain more acetylcholinesterase (AChE) per neuron than do cholinergic neurons of septum. The amount of choline acetyltransferase (ChAT) per cholinergic neuron is approximately the same in all three culture types when grown in the absence of NGF. Second, NGF treatment increases and anti-NGF treatment decreases the number of AChE-positive neurons in cultures of low plating density, suggesting that NGF is able to promote survival of cholinergic neurons of all three areas studied. Third, NGF increases the total length of fibers and the number of branching points of cholinergic neurons in septal cultures but not in cultures of striatum and nucleus basalis. Fourth, NGF treatment increases AChE activity in septal but not in nucleus basalis or striatal cultures, suggesting that AChE activity reflects the extent of the fiber network of cholinergic neurons of all areas. Fifth, NGF treatment produces severalfold elevations in ChAT activity in septal cultures and more modest increases in cultures of nucleus basalis and striatum, suggesting that NGF is able to stimulate ChAT activity also in the absence of a stimulatory effect on survival and fiber growth. Our results demonstrate that, during early development, NGF is able to affect survival and differentiation of all three populations of forebrain cholinergic neurons.(ABSTRACT TRUNCATED AT 400 WORDS)
在中枢神经系统中,神经生长因子(NGF)在早期发育阶段以及成年哺乳动物大脑中影响基底前脑胆碱能神经元。这些神经元位于内侧隔核、布罗卡斜带和迈内特基底核。虽然NGF对隔区胆碱能神经元发育的影响已有充分记录,但关于NGF对基底核胆碱能神经元发育的影响却知之甚少。除了基底前脑胆碱能神经元外,纹状体内还有胆碱能中间神经元,它们构成了一个在解剖学和功能上都不同的胆碱能神经元群体。据报道,这些纹状体中间神经元在早期发育过程中对NGF有反应;然而,尚不清楚NGF对它们发育的影响是否与对隔区胆碱能神经元的影响相似。我们制备了来自胎鼠隔区、纹状体和基底核的解离细胞培养物,并研究了在有或没有NGF的情况下,位于这三个不同区域的胆碱能神经元的发育情况。我们现在报告,首先,与隔区胆碱能神经元相比,纹状体和基底核的胆碱能神经元形成了更广泛的纤维网络,并且每个神经元含有更多的乙酰胆碱酯酶(AChE)。在没有NGF的情况下生长时,所有三种培养类型中每个胆碱能神经元的胆碱乙酰转移酶(ChAT)量大致相同。其次,NGF处理增加而抗NGF处理减少了低接种密度培养物中AChE阳性神经元的数量,这表明NGF能够促进所研究的所有三个区域的胆碱能神经元的存活。第三,NGF增加了隔区培养物中胆碱能神经元纤维的总长度和分支点数量,但在纹状体和基底核培养物中没有增加。第四,NGF处理增加了隔区培养物中的AChE活性,但在基底核或纹状体培养物中没有增加,这表明AChE活性反映了所有区域胆碱能神经元纤维网络的程度。第五,NGF处理使隔区培养物中的ChAT活性提高了几倍,在基底核和纹状体培养物中增加幅度较小,这表明在对存活和纤维生长没有刺激作用的情况下,NGF也能够刺激ChAT活性。我们的结果表明,在早期发育过程中,NGF能够影响前脑所有三个胆碱能神经元群体的存活和分化。(摘要截短至400字)