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Oxygen tension controls the expansion of human CNS precursors and the generation of astrocytes and oligodendrocytes

机译:氧气张力控制着人类中枢神经系统前体细胞的扩增以及星形胶质细胞和少突胶质细胞的产生

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Human neural precursor proliferation and potency is limited by senescence and loss of oligodendrocyte potential. We found that in vitro expansion of human postnatal brain CD133(+) nestin(+) precursors is enhanced at 5% oxygen, while raising oxygen tension to 20% depletes precursors and promotes astrocyte differentiation even in the presence of mitogens. Higher cell densities yielded more astrocytes regardless of oxygen tension. This was reversed by noggin at 5%, but not 20%, oxygen due to a novel repressive effect of low oxygen on bone morphogenetic protein (BMP) signaling. When induced to differentiate by mitogen withdrawal, 5% oxygen-expanded precursors generated 17-fold more oligodendrocytes than cells expanded in 20% oxygen. When precursors were expanded at 5% oxygen and then differentiated at 20% oxygen, oligodendrocyte maturation was further enhanced 2.5-fold. These results indicate that dynamic control of oxygen tension regulates different steps in fate and maturation and may be crucial for treating neurodegenerative diseases. (c) 2007 Elsevier Inc. All rights reserved.
机译:人类神经前体的增殖和效力受衰老和少突胶质细胞潜能的限制。我们发现,人类产后大脑CD133(+)nestin(+)前体的体外扩增在5%的氧气下得到增强,而将氧气张力提高到20%则消耗了前体,甚至在有丝分裂原存在的情况下也促进了星形胶质细胞的分化。较高的细胞密度产生更多的星形胶质细胞,而与氧的张力无关。由于低氧对骨形态发生蛋白(BMP)信号有新的抑制作用,在5%(而不是20%)的氧作用下,这种作用得以逆转。当通过分裂有丝分裂原诱导分化时,5%氧气扩展的前体产生的少突胶质细胞比在20%氧气条件下扩展的细胞少17倍。当前体在5%的氧气中膨胀,然后在20%的氧气中分化时,少突胶质细胞的成熟度进一步提高了2.5倍。这些结果表明,动态控制氧气张力可调节命运和成熟过程的不同步骤,对于治疗神经退行性疾病可能至关重要。 (c)2007 Elsevier Inc.保留所有权利。

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