Selemon Lynn D, Begović Anita, Rakic Pasko
Department of Neurobiology, Yale University School of Medicine, New Haven, Connecticut 06520-8001, USA.
J Comp Neurol. 2009 Aug 1;515(4):454-64. doi: 10.1002/cne.22078.
Neurons in the macaque brain arise from progenitors located near the cerebral ventricles in a temporally segregated manner such that lethal doses of ionizing irradiation, if administered over a discrete time interval, can deplete individual nuclei selectively. A previous study showed that neuron number in the dorsal lateral geniculate nucleus is reduced following early gestational exposure to x-irradiation (Algan and Rakic [1997] J. Comp. Neurol. 12:335-352). Here we examine whether similarly timed irradiation decreases neuron number in three associational thalamic nuclei: mediodorsal (MD), anterior, and pulvinar. Ten macaques were exposed to multiple doses of x-rays (total exposure (175-350 cGy) in early gestation (E33-E42) or midgestation (E70-E90); eight nonirradiated macaques were controls. Only the early-irradiated monkeys, not the midgestationally irradiated animals, exhibited deficits in whole-thalamic neuron (-15%) and glia numbers (-21%) compared with controls. Reduction of neuron number (-26%) and volume (-29%) was particularly pronounced in MD. In contrast, cell number and volume were not significantly decreased in the anterior or pulvinar nuclei following early gestational irradiation. Thus, reduced thalamic neuron number was associated specifically with irradiation in early gestation. Persistence of the thalamic neuronal deficit in adult animals indicates that prenatally deleted neurons had not been replenished during maturation or in adulthood. The selective reduction of MD neuron number also supports the protomap hypothesis that neurons of each thalamic nucleus originate sequentially from separate lines of neuronal stem cells (Rakic [1977a] J. Comp. Neurol. 176:23-52). The early gestationally irradiated macaque is discussed as a potentially useful model for studying the neurodevelopmental pathogenesis of schizophrenia.
猕猴大脑中的神经元由位于脑室附近的祖细胞以时间上分离的方式产生,因此,如果在离散的时间间隔内给予致死剂量的电离辐射,就可以选择性地耗尽单个细胞核。先前的一项研究表明,在妊娠早期暴露于X射线后,背外侧膝状核中的神经元数量会减少(Algan和Rakic [1997] J. Comp. Neurol. 12:335 - 352)。在这里,我们研究了类似时间照射是否会减少三个丘脑联合核中的神经元数量:背内侧(MD)、前核和枕核。十只猕猴在妊娠早期(E33 - E42)或妊娠中期(E70 - E90)接受了多剂量的X射线照射(总照射量为175 - 350 cGy);八只未照射的猕猴作为对照。与对照组相比,只有早期接受照射的猴子,而不是中期接受照射的动物,全丘脑神经元数量(-15%)和神经胶质细胞数量(-21%)出现了减少。MD核中神经元数量(-26%)和体积(-29%)的减少尤为明显。相比之下,妊娠早期照射后,前核或枕核中的细胞数量和体积没有显著减少。因此,丘脑神经元数量的减少与妊娠早期的照射特别相关。成年动物中丘脑神经元缺陷的持续存在表明,产前缺失的神经元在成熟过程或成年期没有得到补充。MD神经元数量的选择性减少也支持了原地图假说,即每个丘脑核的神经元依次起源于不同的神经干细胞系(Rakic [1977a] J. Comp. Neurol. 176:23 - 52)。妊娠早期接受照射的猕猴被讨论为研究精神分裂症神经发育发病机制的潜在有用模型。