尽管生殖中心结构紊乱,神经元和少突胶质细胞存活能力受损,但室管膜下神经干细胞对慢性低氧血症仍有抵抗力。

Hypoxia (Auckland, N.Z.) Pub Date : 2015-06-08 eCollection Date: 2015-01-01 DOI:10.2147/HP.S78248
Xavier d'Anglemont de Tassigny, M Salomé Sirerol-Piquer, Ulises Gómez-Pinedo, Ricardo Pardal, Sonia Bonilla, Vivian Capilla-Gonzalez, Ivette López-López, Francisco Javier De la Torre-Laviana, José Manuel García-Verdugo, José López-Barneo
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引用次数: 0

摘要

慢性低氧血症是一种常见的病症,可导致严重的神经系统改变,这在不适应高海拔环境的居民或慢性阻塞性呼吸系统疾病患者身上都有体现。然而,这种现象的发病机理尚不清楚。我们发现,成年啮齿动物在缺氧环境中暴露数天/数周,动脉血氧张力与慢性低氧血症患者的动脉血氧张力相似时,脑室下神经源龛(脑室下区)会出现部分不可逆的结构紊乱,其特征是神经元和髓鞘轴突移位、上皮细胞层变平以及毛细血管壁变薄。尽管出现了这些异常,但室管膜下区的神经元和少突胶质细胞祖细胞、神经母细胞和神经球形成细胞的数量以及增殖活性均保持不变。这些结果表明,神经干细胞及其未分化的后代对缺氧具有抵抗力。然而,体内和体外实验表明,严重的慢性缺氧会降低新生成神经元和少突胶质细胞的存活率,并损伤髓鞘。这些发现有助于解释缺氧对成人神经发生的影响,并为大脑对持续低氧血症的反应提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Resistance of subventricular neural stem cells to chronic hypoxemia despite structural disorganization of the germinal center and impairment of neuronal and oligodendrocyte survival.

Chronic hypoxemia, as evidenced in de-acclimatized high-altitude residents or in patients with chronic obstructive respiratory disorders, is a common medical condition that can produce serious neurological alterations. However, the pathogenesis of this phenomenon is unknown. We have found that adult rodents exposed for several days/weeks to hypoxia, with an arterial oxygen tension similar to that of chronically hypoxemic patients, manifest a partially irreversible structural disarrangement of the subventricular neurogenic niche (subventricular zone) characterized by displacement of neurons and myelinated axons, flattening of the ependymal cell layer, and thinning of capillary walls. Despite these abnormalities, the number of neuronal and oligodendrocyte progenitors, neuroblasts, and neurosphere-forming cells as well as the proliferative activity in subventricular zone was unchanged. These results suggest that neural stem cells and their undifferentiated progeny are resistant to hypoxia. However, in vivo and in vitro experiments indicate that severe chronic hypoxia decreases the survival of newly generated neurons and oligodendrocytes, with damage of myelin sheaths. These findings help explain the effects of hypoxia on adult neurogenesis and provide new perspectives on brain responsiveness to persistent hypoxemia.

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