Cellerino A, Kohler K
Experimental Ophthalmology, University Eye Hospital, Tübingen, Germany.
J Comp Neurol. 1997 Sep 15;386(1):149-60.
The tyrosine kinase TrkB is a receptor for the neurotrophic factors brain-derived neurotrophic factor (BDNF) and neurotrophin-4 (NT-4). Retinal ganglion cells are responsive to BDNF, and TrkB has been localized in ganglion cells as well as in a subpopulation of amacrine cells in the retina of the chicken and the rat. In the present paper, we analyzed the distribution of TrkB immunoreactivity in the retina of marmoset monkeys, ferrets, rabbits, rats, mice, chickens, pigeons, barn owls, Pseudemys turtles, Xenopus frogs, goldfishes, and carps. TrkB antibodies gave a positive reaction in all of these vertebrates. TrkB immunoreactivity was detected in the majority of retinal ganglion cells. Some amacrine cells also contained TrkB immunoreactivity; they were located mainly at the vitreal border of the inner nuclear layer, and their relative abundance varied in the different species. Until now, no information has been available concerning the neurochemical identity of the amacrine neurons containing TrkB. In some species (marmoset monkeys, rats, pigeons), we observed that the morphology and location of TrkB-immunoreactive amacrine cells was reminiscent of that of the well-described dopaminergic cells. To determine whether dopaminergic amacrine cells contained TrkB immunoreactivity, we therefore performed double-labelling immunohistochemistry by using tyrosine hydroxylase (TH) antibodies in combination with TrkB antibodies in marmoset monkeys, rats, pigeons, Pseudemys turtles, and goldfishes. The most novel finding of the present paper is that, in all of these species, the majority of dopaminergic neurons were found to contain TrkB immunoreactivity. Dopaminergic neurons, on the other hand, represented only a fraction of the TrkB+ amacrine cells. Our data suggest that BDNF and/or NT-4 might modulate expression of TH in the retina and may therefore influence the retinal dopaminergic system. Whatever the action of TrkB ligands on the retinal dopaminergic system, it was conserved during vertebrate evolution.
酪氨酸激酶TrkB是神经营养因子脑源性神经营养因子(BDNF)和神经营养素-4(NT-4)的受体。视网膜神经节细胞对BDNF有反应,并且TrkB已定位在鸡和大鼠视网膜的神经节细胞以及无长突细胞亚群中。在本文中,我们分析了狨猴、雪貂、兔子、大鼠、小鼠、鸡、鸽子、仓鸮、伪龟、非洲爪蟾、金鱼和鲤鱼视网膜中TrkB免疫反应性的分布。TrkB抗体在所有这些脊椎动物中均产生阳性反应。在大多数视网膜神经节细胞中检测到TrkB免疫反应性。一些无长突细胞也含有TrkB免疫反应性;它们主要位于内核层的玻璃体边界,并且其相对丰度在不同物种中有所不同。到目前为止,关于含有TrkB的无长突神经元的神经化学特性尚无相关信息。在一些物种(狨猴、大鼠、鸽子)中,我们观察到TrkB免疫反应性无长突细胞的形态和位置让人联想到已充分描述的多巴胺能细胞。因此,为了确定多巴胺能无长突细胞是否含有TrkB免疫反应性,我们在狨猴、大鼠、鸽子、伪龟和金鱼中使用酪氨酸羟化酶(TH)抗体与TrkB抗体进行了双重标记免疫组织化学实验。本文最新颖的发现是,在所有这些物种中,发现大多数多巴胺能神经元含有TrkB免疫反应性。另一方面,多巴胺能神经元仅占TrkB+无长突细胞的一部分。我们的数据表明,BDNF和/或NT-4可能调节视网膜中TH的表达,因此可能影响视网膜多巴胺能系统。无论TrkB配体对视网膜多巴胺能系统有何种作用,它在脊椎动物进化过程中都是保守的。