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从活鼠脑中分离神经干细胞和少突胶质前体细胞。

Isolation of neural stem and oligodendrocyte progenitor cells from the brain of live rats.

机构信息

Wellcome-MRC Cambridge Stem Cell Institute, University of Cambridge, CB2 0AW Cambridge, UK.

Lab of Developmental Biology, Department of Biology, University of Patras, 26504 Patras, Greece.

出版信息

Stem Cell Reports. 2021 Oct 12;16(10):2534-2547. doi: 10.1016/j.stemcr.2021.08.015. Epub 2021 Sep 23.

Abstract

Postnatal brain neural stem and progenitor cells (NSPCs) cluster in anatomically inaccessible stem cell niches, such as the subependymal zone (SEZ). Here, we describe a method for the isolation of NSPCs from live animals, which we term "milking." The intracerebroventricular injection of a release cocktail, containing neuraminidase, integrin-β1-blocking antibody, and fibroblast growth factor 2, induces the controlled flow of NSPCs in the cerebrospinal fluid, where they are collected via liquid biopsies. Isolated cells retain key in vivo self-renewal properties and their cell-type profile reflects the cell composition of their source area, while the function of the niche is sustained even 8 months post-milking. By changing the target area more caudally, we also isolate oligodendrocyte progenitor cells (OPCs) from the corpus callosum. This novel approach for sampling NSPCs and OPCs paves the way for performing longitudinal studies in experimental animals, for more in vivo relevant cell culture assays, and for future clinical neuro-regenerative applications.

摘要

产后大脑神经干细胞和祖细胞 (NSPCs) 聚集在解剖学上无法到达的干细胞龛位,如室下区 (SEZ)。在这里,我们描述了一种从活体动物中分离 NSPC 的方法,我们称之为“挤奶”。向脑室内注射包含神经氨酸酶、整合素-β1 阻断抗体和碱性成纤维细胞生长因子 2 的释放鸡尾酒,可诱导 NSPC 在脑脊液中的受控流动,然后通过液体活检收集。分离的细胞保留关键的体内自我更新特性,其细胞类型特征反映了其来源区域的细胞组成,而龛位的功能甚至在挤奶后 8 个月仍能维持。通过将靶区更向后改变,我们还可以从胼胝体中分离出少突胶质前体细胞 (OPC)。这种用于采样 NSPC 和 OPC 的新方法为在实验动物中进行纵向研究、进行更符合体内实际情况的细胞培养测定以及未来的临床神经再生应用铺平了道路。

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