Wu C-K, Nagykery N, Hersh L B, Scinto L F M, Geula C
Laboratory for Neurodegenerative and Aging Research, Department of Medicine, Harvard Medical School and Division of Gerontology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Burlington Research Facility, Boston, MA 02215, USA.
Neuroscience. 2003;120(1):249-59. doi: 10.1016/s0306-4522(03)00248-3.
A significant number of the cholinergic neurons in the basal forebrain of the primate, but not the rodent brain contain the calcium binding protein calbindin-D28k (CB). Previous experiments in our laboratory have demonstrated a substantial age-related loss of CB from the human basal forebrain cholinergic neurons (BFCN). The present study investigated the possible age-related loss of CB from the BFCN in a non-human primate species, the common marmoset (Callithrix jacchus). Quantitative analysis of matching sections as well as unbiased stereological determination of neuronal number were used in 16 adult marmosets ranging in age between 2 and 15 years. No significant changes were observed in the number of choline acetyltransferase-positive BFCN when a group of young animals (< or =4 years) was compared with a 6-8-year-old group and a 9-15-year-old group. Similarly, no age-related changes were observed in Nissl-stained magnocellular basal forebrain (putatively cholinergic) neurons. In contrast, the BFCN of the two older groups of animals displayed a significant loss of CB. The age-related loss of CB occurred in all sectors of the BFCN, but was greatest in the anterior sector of this cell group. The CB loss was neurochemically specific since the BFCN in the older groups of animals continued to express other markers such as high and low affinity neurotrophin receptors. The age-related loss of CB from the marmoset BFCN was also regionally selective as CB positive neurons in other structures, such as the cerebral cortex and the striatum displayed no apparent age-related changes. These results indicate that the marmoset BFCN display a significant and selective age-related loss of CB reminiscent of that observed in the human. Therefore, the common marmoset represents an appropriate animal model in which the consequences of BFCN CB loss can be investigated in depth. Loss of CB from the aged BFCN is likely to reduce the capacity of these neurons to buffer intracellular calcium and to leave them vulnerable to insults which can result in increased calcium levels. The vulnerability of the CB-negative BFCN in the aged marmoset to various insults which disturb calcium homeostasis remains to be investigated.
灵长类动物前脑基底中的大量胆碱能神经元含有钙结合蛋白钙结合蛋白-D28k(CB),但啮齿动物大脑中的此类神经元则不含。我们实验室之前的实验表明,人类前脑基底胆碱能神经元(BFCN)中CB会随着年龄增长而大量减少。本研究调查了非人类灵长类动物普通狨猴(Callithrix jacchus)的BFCN中CB是否可能随年龄增长而减少。对16只年龄在2至15岁之间的成年狨猴进行了匹配切片的定量分析以及神经元数量的无偏立体学测定。将一组幼龄动物(≤4岁)与6至8岁组和9至15岁组进行比较时,未观察到胆碱乙酰转移酶阳性BFCN数量有显著变化。同样,在尼氏染色的大细胞前脑基底(推测为胆碱能)神经元中也未观察到与年龄相关的变化。相比之下,两组年龄较大的动物的BFCN显示出CB显著减少。CB随年龄增长的减少发生在BFCN的所有区域,但在该细胞群的前部区域最为明显。CB的减少具有神经化学特异性,因为年龄较大组动物的BFCN继续表达其他标志物,如高亲和力和低亲和力神经营养因子受体。狨猴BFCN中CB随年龄增长的减少在区域上也具有选择性,因为大脑皮层和纹状体等其他结构中的CB阳性神经元未显示出明显的与年龄相关的变化。这些结果表明,狨猴的BFCN显示出与年龄相关的显著且选择性的CB减少,这与在人类中观察到的情况类似。因此,普通狨猴是一种合适的动物模型,可用于深入研究BFCN中CB缺失的后果。老年BFCN中CB的缺失可能会降低这些神经元缓冲细胞内钙的能力,并使它们容易受到可导致钙水平升高的损伤。老年狨猴中CB阴性BFCN对各种干扰钙稳态的损伤的易感性仍有待研究。