Buchet Delphine, Buc-Caron Marie-Hélène, Sabaté Olivier, Lachapelle François, Mallet Jacques
Laboratoire de Génétique Moléculaire de la Neurotransmission et des Processus Neurodégénératifs, CNRS UMR 7091, Bâtiment CERVI, Hôpital de la Pitié Salpêtrière, Paris, France.
J Neurosci Res. 2002 May 1;68(3):276-83. doi: 10.1002/jnr.10183.
We assessed the developmental potential of human telencephalic progenitor cells, with and without previous amplification in vitro, following grafting into the nonlesioned adult mouse CNS. Cell suspensions, shown to contain neuroepithelium-like and neuroblast-like cells, were injected into the subventricular zone (SVZ) and the striatum. These two regions were selected for comparative studies because one, the SVZ, is mitotically active, whereas the other, the striatum, is mitotically inactive. In situ hybridization with a human-specific Alu probe showed that the cells survived for up to 30 weeks in both targets and migrated away from the injection site. Fresh cells continued to proliferate and gave rise to very extended grafts before differentiating into neurons and glia. We further show that, when grown in vitro prior to grafting, human cells acquired new properties: Their proliferation was very limited, and they differentiated more rapidly. This study therefore provides new information about the use of these cells, which are a potential tool for both cellular and gene therapy.
我们评估了人类端脑祖细胞在移植到未受损成年小鼠中枢神经系统后(无论之前是否在体外扩增)的发育潜力。将已证明含有神经上皮样细胞和成神经细胞样细胞的细胞悬液注入脑室下区(SVZ)和纹状体。选择这两个区域进行比较研究是因为其中一个区域SVZ有活跃的有丝分裂,而另一个区域纹状体则无有丝分裂活性。用人类特异性Alu探针进行原位杂交显示,这些细胞在两个靶点中存活长达30周,并从注射部位迁移出去。新鲜细胞持续增殖并形成非常广泛的移植物,然后分化为神经元和神经胶质细胞。我们进一步表明,在移植前于体外培养时,人类细胞获得了新特性:它们的增殖非常有限,且分化更快。因此,本研究提供了有关这些细胞用途的新信息,这些细胞是细胞治疗和基因治疗的潜在工具。