Kellermann Odile, Lafay-Chebassier Claire, Ermonval Myriam, Lehmann Sylvain, Mouillet-Richard Sophie
Laboratoire de différenciation cellulaire et prions, CNRS UPR 1983-Institut Pasteur, BP 8, 94801 Villejuif, France.
C R Biol. 2002 Jan;325(1):9-15. doi: 10.1016/s1631-0691(02)01387-2.
A strategy based upon the introduction of an adenovirus-SV40 plasmid into multipotential cells was designed to immortalize clones displaying properties of lineage stem cells. The murine 1C11 cell line behaves as a neuroepithelial progenitor. Upon appropriate induction, almost 100% of 1C11 precursor cells develop neurite extensions and convert into either serotonergic or noradrenergic neurons. The two mutually exclusive neuronal programs are autoregulated by serotonergic or adrenergic receptors. PrPc is constitutively expressed by 1C11 cells. Antibody-mediated cross-linking of PrPc promotes the dephosphorylation of the tyrosine kinase Fyn associated to a Fyn kinase activation. The coupling of PrPc to Fyn is dependent on caveolin-1. It is restricted to the fully differentiated serotonergic or noradrenergic cells and occurs mainly at neurites. Thus, PrPc may represent a signal transduction protein which may fine-tune neuronal functions. Since the 1C11 stem cell supports prion replication, it may provide a tool to investigate whether PrPSc accumulation interferes with PrPc signalling activity.
设计了一种基于将腺病毒-SV40质粒导入多能细胞的策略,以使表现出谱系干细胞特性的克隆永生化。小鼠1C11细胞系表现为神经上皮祖细胞。经过适当诱导,几乎100%的1C11前体细胞会形成神经突延伸,并转化为5-羟色胺能或去甲肾上腺素能神经元。这两个相互排斥的神经元程序由5-羟色胺能或肾上腺素能受体自动调节。1C11细胞组成性表达PrPc。抗体介导的PrPc交联促进与Fyn激酶激活相关的酪氨酸激酶Fyn的去磷酸化。PrPc与Fyn的偶联依赖于小窝蛋白-1。它仅限于完全分化的5-羟色胺能或去甲肾上腺素能细胞,主要发生在神经突处。因此,PrPc可能代表一种信号转导蛋白,它可能对神经元功能进行微调。由于1C11干细胞支持朊病毒复制,它可能提供一种工具来研究PrPSc积累是否会干扰PrPc信号活性。