Kizil Caghan
1German Centre for Neurodegenerative Diseases (DZNE) Dresden, Helmholtz Association, Arnoldstrasse 18, 01307 Dresden, Germany.
2Center for Regenerative Therapies Dresden (CRTD), TU Dresden, Fetscherstrasse 105, 01307 Dresden, Germany.
Curr Pathobiol Rep. 2018;6(1):71-77. doi: 10.1007/s40139-018-0158-x. Epub 2018 Jan 16.
The purpose of this study is to review the current knowledge on the damage-induced molecular programs that underlie the regenerative ability in zebrafish brain.
Neural stem cells are the reservoir for new neurons during development and regeneration of the vertebrate brains. Pathological conditions such as neurodegenerative diseases hamper neural stem cell plasticity and neurogenic outcome in humans, whereas adult zebrafish brain can enhance proliferation and neurogenic capacity of its neural stem cells despite the incipient pathology. Evidence suggests that zebrafish uses damage-induced molecular programs to enable neural stem cells to efficiently initiate regeneration. Since this aptitude may be harnessed for regenerative therapies in human brain, understanding the molecular programs regulating neural stem cell proliferation and quiescence in zebrafish is of utmost importance for clinical efforts.
Specific molecular programs that are different than those in the homeostatic conditions regulate adult zebrafish neural stem cell plasticity and the regenerative capacity after injury and neurodegeneration. These programs can serve as candidates for stem cell-based regenerative therapies in humans.
本研究旨在回顾目前关于斑马鱼大脑再生能力背后损伤诱导分子程序的知识。
神经干细胞是脊椎动物大脑发育和再生过程中新神经元的来源。诸如神经退行性疾病等病理状况会阻碍人类神经干细胞的可塑性和神经发生结果,而成体斑马鱼大脑尽管存在初期病理状况,却能增强其神经干细胞的增殖和神经发生能力。有证据表明,斑马鱼利用损伤诱导分子程序使神经干细胞能够有效地启动再生。由于这种能力可用于人类大脑的再生治疗,了解调节斑马鱼神经干细胞增殖和静止的分子程序对于临床研究至关重要。
与稳态条件下不同的特定分子程序调节成体斑马鱼神经干细胞的可塑性以及损伤和神经退行性变后的再生能力。这些程序可作为人类基于干细胞的再生治疗的候选方案。