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星形胶质细胞 N-myc 下游调节基因 2 可保护大脑免受中风引起的脑水肿。

Astroglial N-myc downstream-regulated gene 2 protects the brain from cerebral edema induced by stroke.

机构信息

Department of Anesthesiology, The Seventh Medical Center of Chinese PLA General Hospital, Beijing, China.

Department of Anesthesiology and Perioperative Medicine, Xijing Hospital, The Air Force Military Medical University, Xi'an, China.

出版信息

Glia. 2021 Feb;69(2):281-295. doi: 10.1002/glia.23888. Epub 2020 Jul 11.

DOI:10.1002/glia.23888
PMID:32652708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7754347/
Abstract

Brain edema is a grave complication of brain ischemia and is the main cause of herniation and death. Although astrocytic swelling is the main contributor to cytotoxic edema, the molecular mechanism involved in this process remains elusive. N-myc downstream-regulated gene 2 (NDRG2), a well-studied tumor suppressor gene, is mainly expressed in astrocytes in mammalian brains. Here, we found that NDRG2 deficiency leads to worsened cerebral edema, imbalanced Na transfer, and astrocyte swelling after ischemia. We also found that NDRG2 deletion in astrocytes dramatically changed the expression and distribution of aquaporin-4 and Na -K -ATPase β1, which are strongly associated with cell polarity, in the ischemic brain. Brain edema and astrocyte swelling were significantly alleviated by rescuing the expression of astrocytic Na -K -ATPase β1 in NDRG2-knockout mouse brains. In addition, the upregulation of astrocytic NDRG2 by lentiviral constructs notably attenuated brain edema, astrocytic swelling, and blood-brain barrier destruction. Our results indicate a particular role of NDRG2 in maintaining astrocytic polarization to facilitate Na and water transfer balance and to protect the brain from ischemic edema. These findings provide insight into NDRG2 as a therapeutic target in cerebral edema.

摘要

脑水肿是脑缺血的严重并发症,也是脑疝和死亡的主要原因。虽然星形胶质细胞肿胀是细胞毒性水肿的主要原因,但该过程涉及的分子机制仍不清楚。N-myc 下游调节基因 2(NDRG2)是一种研究较多的肿瘤抑制基因,主要在哺乳动物大脑的星形胶质细胞中表达。在这里,我们发现 NDRG2 缺乏会导致缺血后脑水肿加重、Na 转移失衡和星形胶质细胞肿胀。我们还发现,星形胶质细胞中 NDRG2 的缺失会显著改变水通道蛋白-4 和 Na+-K+-ATP 酶 β1 的表达和分布,这与细胞极性密切相关。通过挽救 NDRG2 敲除小鼠大脑中星形胶质细胞的 Na+-K+-ATP 酶 β1 的表达,显著减轻了脑水肿和星形胶质细胞肿胀。此外,慢病毒构建体上调星形胶质细胞 NDRG2 明显减轻脑水肿、星形胶质细胞肿胀和血脑屏障破坏。我们的结果表明 NDRG2 在维持星形胶质细胞极性以促进 Na 和水转移平衡以及保护大脑免受缺血性水肿方面具有特殊作用。这些发现为 NDRG2 作为脑水肿的治疗靶点提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/83a3b446e630/GLIA-69-281-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/1873abba2807/GLIA-69-281-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/481c01b69b1e/GLIA-69-281-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/d93653470cb1/GLIA-69-281-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/36cd9a97a4e0/GLIA-69-281-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/83a3b446e630/GLIA-69-281-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/1873abba2807/GLIA-69-281-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/481c01b69b1e/GLIA-69-281-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/d93653470cb1/GLIA-69-281-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/36cd9a97a4e0/GLIA-69-281-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b211/7754347/83a3b446e630/GLIA-69-281-g005.jpg

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