Department of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom; Present address: St George's University Hospitals NHS Foundation Trust London United Kingdom.
Department of Clinical and Experimental Epilepsy UCL Institute of Neurology National Hospital for Neurology and Neurosurgery London WC1N 3BG United Kingdom.
Ann Clin Transl Neurol. 2016 Apr 12;3(5):314-30. doi: 10.1002/acn3.297. eCollection 2016 May.
PAX6 is a pleiotropic transcription factor essential for the development of several tissues including the eyes, central nervous system, and some endocrine glands. Recently it has also been shown to be important for the maintenance and functioning of corneal and pancreatic tissues in adults. We hypothesized that PAX6 is important for the maintenance of brain integrity in humans, and that adult heterozygotes may have abnormalities of cortical patterning analogous to those found in mouse models.
We used advanced magnetic resonance imaging techniques, including surface-based morphometry and region-of-interest analysis in adult humans heterozygously mutated for PAX6 mutations (n = 19 subjects and n = 21 controls). Using immunohistochemistry, we also studied PAX6 expression in the adult brain tissue of healthy subjects (n = 4) and patients with epilepsy (n = 42), some of whom had focal injuries due to intracranial electrode track placement (n = 17).
There were significant reductions in frontoparietal cortical area after correcting for age and intracranial volume. A greater decline in thickness of the frontoparietal cortex with age, in subjects with PAX6 mutations compared to controls, correlated with age-corrected, accelerated decline in working memory. These results also demonstrate genotypic effects: those subjects with the most severe genotypes have the most widespread differences compared with controls. We also demonstrated significant increases in PAX6-expressing cells in response to acute injury in the adult human brain.
These findings suggest a role for PAX6 in the maintenance and consequent functioning of the adult brain, homologous to that found in other tissues. This has significant implications for the understanding and treatment of neurodegenerative diseases.
PAX6 是一种多效转录因子,对包括眼睛、中枢神经系统和一些内分泌腺在内的几种组织的发育至关重要。最近,它也被证明对成年角膜和胰腺组织的维持和功能很重要。我们假设 PAX6 对人类大脑完整性的维持很重要,并且成年杂合子可能存在类似于在小鼠模型中发现的皮质模式异常。
我们使用了先进的磁共振成像技术,包括表面形态计量学和感兴趣区域分析,研究了成年 PAX6 突变杂合子的人类(n = 19 名受试者和 n = 21 名对照)。我们还通过免疫组织化学,研究了健康受试者(n = 4)和癫痫患者(n = 42)的成年脑组织中的 PAX6 表达,其中一些患者由于颅内电极轨迹放置而有局灶性损伤(n = 17)。
在校正年龄和颅内体积后,额顶皮质面积明显减少。与对照组相比,PAX6 突变受试者的额顶皮质厚度随年龄的下降更大,与工作记忆的年龄校正加速下降相关。这些结果还表明存在基因型效应:与对照组相比,那些具有最严重基因型的受试者与对照组的差异最广泛。我们还证明了急性损伤后成年人大脑中 PAX6 表达细胞的显著增加。
这些发现表明 PAX6 在维持和随后的成年大脑功能中起作用,与在其他组织中发现的作用相似。这对理解和治疗神经退行性疾病具有重要意义。