Dopeso-Reyes Iria G, Rico Alberto J, Roda Elvira, Sierra Salvador, Pignataro Diego, Lanz Maria, Sucunza Diego, Chang-Azancot Luis, Lanciego Jose L
Center for Applied Medical Research (CIMA), University of Navarra Medical College Pamplona, Spain ; Centro de Investigación Biomédica en Red Sobre Enfermedades Neurodegenerativas (CIBERNED) Pamplona, Spain.
Center for Applied Medical Research (CIMA), University of Navarra Medical College Pamplona, Spain.
Front Neuroanat. 2014 Dec 3;8:146. doi: 10.3389/fnana.2014.00146. eCollection 2014.
Calbindin (CB) is a calcium binding protein reported to protect dopaminergic neurons from degeneration. Although a direct link between CB content and differential vulnerability of dopaminergic neurons has long been accepted, factors other than CB have also been suggested, particularly those related to the dopamine transporter. Indeed, several studies have reported that CB levels are not causally related to the differential vulnerability of dopaminergic neurons against neurotoxins. Here we have used dual stains for tyrosine hydroxylase (TH) and CB in 3 control and 3 MPTP-treated monkeys to visualize dopaminergic neurons in the ventral tegmental area (VTA) and in the dorsal and ventral tiers of the substantia nigra pars compacta (SNcd and SNcv) co-expressing TH and CB. In control animals, the highest percentages of co-localization were found in VTA (58.2%), followed by neurons located in the SNcd (34.7%). As expected, SNcv neurons lacked CB expression. In MPTP-treated animals, the percentage of CB-ir/TH-ir neurons in the VTA was similar to control monkeys (62.1%), whereas most of the few surviving neurons in the SNcd were CB-ir/TH-ir (88.6%). Next, we have elucidated the presence of CB within identified nigrostriatal and nigroextrastriatal midbrain dopaminergic projection neurons. For this purpose, two control monkeys received one injection of Fluoro-Gold into the caudate nucleus and one injection of cholera toxin (CTB) into the postcommissural putamen, whereas two more monkeys were injected with CTB into the internal division of the globus pallidus (GPi). As expected, all the nigrocaudate- and nigroputamen-projecting neurons were TH-ir, although surprisingly, all of these nigrostriatal-projecting neurons were negative for CB. Furthermore, all the nigropallidal-projecting neurons co-expressed both TH and CB. In summary, although CB-ir dopaminergic neurons seem to be less prone to MPTP-induced degeneration, our data clearly demonstrated that these neurons are not giving rise to nigrostriatal projections and indeed CB-ir/TH-ir neurons only originate nigroextrastriatal projections.
钙结合蛋白(CB)是一种钙结合蛋白,据报道它能保护多巴胺能神经元免于退化。尽管长期以来人们一直认为CB含量与多巴胺能神经元的不同易损性之间存在直接联系,但也有人提出了除CB之外的其他因素,特别是那些与多巴胺转运体相关的因素。事实上,几项研究报告称,CB水平与多巴胺能神经元对神经毒素的不同易损性并无因果关系。在这里,我们对3只对照猴子和3只经1-甲基-4-苯基-1,2,3,6-四氢吡啶(MPTP)处理的猴子的酪氨酸羟化酶(TH)和CB进行双重染色,以可视化腹侧被盖区(VTA)以及黑质致密部背侧和腹侧层(SNcd和SNcv)中共表达TH和CB的多巴胺能神经元。在对照动物中,共定位百分比最高的是VTA(58.2%),其次是位于SNcd的神经元(34.7%)。正如预期的那样,SNcv神经元缺乏CB表达。在经MPTP处理的动物中,VTA中CB免疫反应性/TH免疫反应性神经元的百分比与对照猴子相似(62.1%),而SNcd中少数存活的神经元大多是CB免疫反应性/TH免疫反应性(88.6%)。接下来,我们阐明了在已确定的黑质纹状体和黑质纹状体以外的中脑多巴胺能投射神经元中CB的存在情况。为此,两只对照猴子分别向尾状核注射一次氟金,向连合后壳核注射一次霍乱毒素B亚单位(CTB),而另外两只猴子则向苍白球内侧部(GPi)注射CTB。正如预期的那样,所有投射到黑质尾状核和黑质壳核的神经元都是TH免疫反应性的,尽管令人惊讶的是,所有这些投射到黑质纹状体的神经元CB均为阴性。此外,所有投射到黑质苍白球的神经元都共表达TH和CB。总之,尽管CB免疫反应性多巴胺能神经元似乎不太容易受到MPTP诱导的退化影响,但我们的数据清楚地表明,这些神经元不会产生黑质纹状体投射,实际上CB免疫反应性/TH免疫反应性神经元仅起源于黑质纹状体以外的投射。