No observed effect on brain vasculature of Alzheimer's disease-related mutations in the zebrafish presenilin 1 gene

被引:2
|
作者
Barthelson, Karissa [1 ]
Newman, Morgan [1 ]
Nowell, Cameron J. [2 ]
Lardelli, Michael [1 ]
机构
[1] Univ Adelaide, Sch Biol Sci, Alzheimers Dis Genet Lab, North Terrace, Adelaide, SA 5005, Australia
[2] Monash Univ, Monash Inst Pharmaceut Sci, Drug Discovery Biol, Parkville, Vic 3058, Australia
基金
英国医学研究理事会;
关键词
Zebrafish; Vasculature; Confocal laser scanning microscopy; 3D reconstruction;
D O I
10.1186/s13041-021-00734-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Previously, we found that brains of adult zebrafish heterozygous for Alzheimer's disease-related mutations in their presenilin 1 gene (psen1, orthologous to human PSEN1) show greater basal expression levels of hypoxia responsive genes relative to their wild type siblings under normoxia, suggesting hypoxic stress. In this study, we investigated whether this might be due to changes in brain vasculature. We generated and compared 3D reconstructions of GFP-labelled blood vessels of the zebrafish forebrain from heterozygous psen1 mutant zebrafish and their wild type siblings. We observed no statistically significant differences in vessel density, surface area, overall mean diameter, overall straightness, or total vessel length normalised to the volume of the telencephalon. Our findings do not support that changes in vascular morphology are responsible for the increased basal expression of hypoxia responsive genes in psen1 heterozygous mutant brains.
引用
收藏
页数:4
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