Hower Molly, Bondarenko Viktoriya, Emborg Marina E, Metzger Jeanette M
Wisconsin National Primate Research Center, University of Wisconsin - Madison, Madison, WI, USA.
Department of Medical Physics, University of Wisconsin - Madison, Madison, WI, USA.
Next Res. 2025 Sep;2(3). doi: 10.1016/j.nexres.2025.100624. Epub 2025 Jul 16.
Transgenic pigs are emerging as large animal models for biomedical research. Green fluorescent protein (GFP)-expressing transgenic reporter pigs (GFP-Tg; NSRRC:0016 GFP ) express GFP via the ubiquitous pCAGG promoter. Their level of GFP expression across brain regions has not yet been evaluated. Brain tissue sections from GFP-Tg animals were immunostained against GFP and the neuronal marker NeuN, or against GFP, NeuN, and the dopaminergic neuronal marker tyrosine hydroxylase (TH). The presence and intensity of neuronal GFP expression was evaluated in the amygdala, caudate, hippocampus, primary motor cortex (M1), putamen, and substantia nigra pars compacta (SNpc). Images from each region were captured, and individual neurons were counted and rated based on their intensity of GFP expression as being GFP positive (GFP+), equal (GFP=) to neuropil, dim (GFPd), or negative (GFP-). Nearly all neurons in the amygdala (99.2%), caudate (99.0%), hippocampus (99.7%), M1 (99.4%), and putamen, (98.8%) showed high GFP-immunoreactivity (combined GFP+ and GFP=), in contrast to the SNpc, which had significantly less (61.4%; p=0.0266). The number of GFP- neurons was significantly higher in the SNpc than in the amygdala (p =0.0342), hippocampus (p=0.0366), and M1 (p=0.0437). Overall, this study demonstrates high neuronal GFP expression in the GFP-Tg reporter pig, but with variability between brain regions, particularly decreased GFP expression in dopaminergic nigral neurons. Future research utilizing this model, such as studies to evaluate the efficacy of genome-editors for Parkinson's disease through their ability to turn off GFP expression in the nigrostriatal system, should account for this neuronal GFP-expression variability.
转基因猪正成为生物医学研究的大型动物模型。表达绿色荧光蛋白(GFP)的转基因报告猪(GFP-Tg;NSRRC:0016 GFP)通过普遍存在的pCAGG启动子表达GFP。其在大脑各区域的GFP表达水平尚未得到评估。对来自GFP-Tg动物的脑组织切片进行针对GFP和神经元标志物NeuN的免疫染色,或针对GFP、NeuN和多巴胺能神经元标志物酪氨酸羟化酶(TH)的免疫染色。在杏仁核、尾状核、海马体、初级运动皮层(M1)、壳核和黑质致密部(SNpc)中评估神经元GFP表达的存在和强度。拍摄每个区域的图像,并根据单个神经元的GFP表达强度将其计数并评定为GFP阳性(GFP+)、与神经毡相等(GFP=)、暗淡(GFPd)或阴性(GFP-)。杏仁核(99.2%)、尾状核(99.0%)、海马体(99.7%)、M1(99.4%)和壳核(98.8%)中几乎所有神经元都显示出高GFP免疫反应性(GFP+和GFP=合并),相比之下,SNpc中的比例明显较低(61.4%;p=0.0266)。SNpc中GFP-神经元的数量显著高于杏仁核(p =0.0342)、海马体(p=0.0366)和M1(p=0.0437)。总体而言,本研究表明GFP-Tg报告猪中神经元GFP表达较高,但大脑区域之间存在差异,特别是多巴胺能黑质神经元中的GFP表达降低。利用该模型的未来研究,如通过基因组编辑在黑质纹状体系统中关闭GFP表达的能力来评估帕金森病基因组编辑器疗效的研究,应考虑这种神经元GFP表达的变异性。