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损伤大脑中的反应性神经胶质通过 Sonic Hedgehog 信号通路获得干细胞特性。[已更正]

Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog. [corrected].

机构信息

Physiological Genomics, Institute of Physiology, Ludwig-Maximilians University Munich, D-80336, Germany.

出版信息

Cell Stem Cell. 2013 Apr 4;12(4):426-39. doi: 10.1016/j.stem.2013.01.019.

Abstract

As a result of brain injury, astrocytes become activated and start to proliferate in the vicinity of the injury site. Recently, we had demonstrated that these reactive astrocytes, or glia, can form self-renewing and multipotent neurospheres in vitro. In the present study, we demonstrate that it is only invasive injury, such as stab wounding or cerebral ischemia, and not noninvasive injury conditions, such as chronic amyloidosis or induced neuronal death, that can elicit this increase in plasticity. Furthermore, we find that Sonic hedgehog (SHH) is the signal that acts directly on the astrocytes and is necessary and sufficient to elicit the stem cell response both in vitro and in vivo. These findings provide a molecular basis for how cells with neural stem cell lineage emerge at sites of brain injury and imply that the high levels of SHH known to enter the brain from extraneural sources after invasive injury can trigger this response.

摘要

由于脑损伤,星形胶质细胞在损伤部位附近被激活并开始增殖。最近,我们已经证明,这些反应性星形胶质细胞或神经胶质细胞可以在体外形成自我更新和多能性的神经球。在本研究中,我们证明只有侵袭性损伤,如刺伤或脑缺血,而不是非侵袭性损伤条件,如慢性淀粉样变性或诱导的神经元死亡,才能引起这种可塑性的增加。此外,我们发现 Sonic hedgehog (SHH) 是直接作用于星形胶质细胞的信号,无论是在体外还是体内,都是引发干细胞反应所必需和充分的。这些发现为具有神经干细胞谱系的细胞如何在脑损伤部位出现提供了分子基础,并暗示侵袭性损伤后从神经外来源进入大脑的高水平 SHH 可以触发这种反应。

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