Paniagua-Herranz Lucía, Menéndez-Méndez Aida, Gómez-Villafuertes Rosa, Olivos-Oré Luis A, Biscaia Miguel, Gualix Javier, Pérez-Sen Raquel, Delicado Esmerilda G, Artalejo Antonio R, Miras-Portugal María Teresa, Ortega Felipe
Departament of Biochemistry and Molecular Biology, Faculty of Veterinary, Universidad Complutense de Madrid (UCM), Madrid, Spain; Instituto Universitario de Investigación en Neuroquímica (IUIN), Madrid, Spain; Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.
Instituto Universitario de Investigación en Neuroquímica (IUIN), Madrid, Spain; Instituto de Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain; Department of Pharmacology and Toxicology, Faculty of Veterinary, Universidad Complutense de Madrid, Madrid, Spain.
Stem Cell Reports. 2020 Nov 10;15(5):1080-1094. doi: 10.1016/j.stemcr.2020.09.007. Epub 2020 Oct 15.
Little is known about the intrinsic specification of postnatal cerebellar neural stem cells (NSCs) and to what extent they depend on information from their local niche. Here, we have used an adapted cell preparation of isolated postnatal NSCs and live imaging to demonstrate that cerebellar progenitors maintain their neurogenic nature by displaying hallmarks of NSCs. Furthermore, by using this preparation, all the cell types produced postnatally in the cerebellum, in similar relative proportions to those observed in vivo, can be monitored. The fact that neurogenesis occurs in such organized manner in the absence of signals from the local environment, suggests that cerebellar lineage progression is to an important extent governed by cell-intrinsic or pre-programmed events. Finally, we took advantage of the absence of the niche to assay the influence of the vesicular nucleotide transporter inhibition, which dramatically reduced the number of NSCs in vitro by promoting their progression toward neurogenesis.
关于出生后小脑神经干细胞(NSCs)的内在特化以及它们在多大程度上依赖于其局部微环境的信息,人们了解甚少。在这里,我们使用了一种经过改良的分离出生后NSCs的细胞制备方法和实时成像技术,以证明小脑祖细胞通过展现NSCs的特征来维持其神经发生特性。此外,通过使用这种制备方法,可以监测出生后小脑产生的所有细胞类型,其相对比例与在体内观察到的相似。在没有来自局部环境信号的情况下神经发生以如此有组织的方式发生,这一事实表明小脑谱系进展在很大程度上受细胞内在或预编程事件的支配。最后,我们利用微环境缺失来检测囊泡核苷酸转运体抑制的影响,该抑制通过促进NSCs向神经发生的进展显著减少了体外NSCs的数量。