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Myelin Basic Protein Regulates Primitive and Definitive Neural Stem Cell Proliferation from the Adult Spinal Cord

机译:髓鞘碱性蛋白质从成年脊髓调节原始和明确的神经干细胞增殖

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The adult mammalian forebrain comprises two distinct populations of neural stem cells (NSCs): rare, Oct4 positive, primitive NSCs (pNSCs) and definitive NSC (dNSC) which are more abundant and express GFAP. The pNSCs are upstream of the dNSCs in the neural stem cell lineage. Herein we show that pNSC and dNSC populations can also be isolated from the developing and adult spinal cord. Spinal cord derived pNSCs are similarly rare, Oct4 expressing cells that are responsive to leukemia inhibitory factor and dNSCs are 4-5X more abundant and express GFAP. We demonstrate that myelin basic protein (MBP) is inhibitory to both pNSC and dNSC derived colony formation. Similar to what is seen in the adult forebrain following injury, spinal cord injury results in a significant increase in the size of the dNSC and pNSC pools. Hence, both primitive and definitive neural stem cells can be isolated from along the embryonic and adult neuraxis in vivo and their behavior is regulated by MBP and injury.
机译:成年哺乳动物前脑包含两个不同的神经干细胞(NSC)群:罕见的,OCT4阳性,原始NSCs(PNSCs)和最终的NSC(DNSC),其更丰富和表达GFAP。 PNSC在神经干细胞谱系中的DNSCs的上游。 在此,我们表明PNSC和DNSC群体也可以从显影和成人脊髓中分离。 脊髓衍生的PNSCS类似地罕见,OCT4表达对白血病抑制因子和DNSCs的响应性的细胞均为4-5倍,并表达GFAP。 我们证明髓鞘碱性蛋白(MBP)是PNSC和DNSC衍生菌落形成的抑制作用。 类似于损伤后成人前脑中所见的内容,脊髓损伤导致DNSC和PNSC池大小的显着增加。 因此,原始和明确的神经干细胞可以沿着胚胎和成年神经体内分离体内,其行为由MBP和损伤调节。

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