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同源盒基因神经保护胚胎神经元细胞。

Homeoprotein Neuroprotection of Embryonic Neuronal Cells.

机构信息

Centre for Interdisciplinary Research in Biology (CIRB), Collège de France, CNRS UMR 7241/INSERM U1050, PSL Research University, Labex Memolife Paris Science et Lettres, 75005 Paris, France.

BrainEver, 75012 Paris, France.

出版信息

eNeuro. 2019 Sep 26;6(5). doi: 10.1523/ENEURO.0061-19.2019. Print 2019 Sep/Oct.

DOI:10.1523/ENEURO.0061-19.2019
PMID:31451602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6763833/
Abstract

Most homeoprotein transcription factors have a highly conserved internalization domain used in intercellular transfer. Internalization of homeoproteins ENGRAILED1 or ENGRAILED2 promotes the survival of adult dopaminergic cells, whereas that of OTX2 protects adult retinal ganglion cells. Here we characterize the neuroprotective activity of several homeoproteins in response to HO Protection is observed with ENGRAILED1, ENGRAILED2, OTX2, GBX2, and LHX9 on midbrain and striatal embryonic neurons, whereas cell-permeable c-MYC shows no protective effects. Therefore, five homeoproteins belonging to three different classes (ANTENNAPEDIA, PAIRED, and LIM) share the ability to protect embryonic neurons from midbrain and striatum. Because midbrain and striatal neurons do not express the same repertoire of the four proteins, a lack of neuronal specificity together with a general protective activity can be proposed. Interestingly, hEN1 and GBX2 provided protection to primary midbrain astrocytes but not to non-neural cells, including mouse embryo fibroblasts, macrophages or HeLa cells. For the four proteins, protection against cell death correlated with a reduction in the number of HO-induced DNA break foci in midbrain and striatal neurons. In conclusion, within the limit of the number of cell types and homeoproteins tested, homeoprotein protection against oxidative stress-induced DNA breaks and death is specific to neurons and astrocytes but shows no homeoprotein or neuronal type specificity.

摘要

大多数同源盒转录因子都具有高度保守的内化结构域,用于细胞间转移。同源盒蛋白 ENGRAILED1 或 ENGRAILED2 的内化可促进成年多巴胺能细胞的存活,而 OTX2 的内化则可保护成年视网膜神经节细胞。在这里,我们描述了几种同源盒蛋白在应对 HO 时的神经保护活性。在中脑和纹状体胚胎神经元中观察到 ENGRAILED1、ENGRAILED2、OTX2、GBX2 和 LHX9 的保护作用,而细胞通透型 c-MYC 则没有保护作用。因此,属于三个不同类别的五种同源盒蛋白(ANTENNAPEDIA、PAIRED 和 LIM)具有保护中脑和纹状体胚胎神经元的能力。由于中脑和纹状体神经元不表达这四种蛋白的相同组合,因此可以提出缺乏神经元特异性和普遍的保护活性。有趣的是,hEN1 和 GBX2 为原代中脑星形胶质细胞提供了保护,但不能为非神经细胞(包括小鼠胚胎成纤维细胞、巨噬细胞或 HeLa 细胞)提供保护。对于这四种蛋白,细胞死亡的保护与中脑和纹状体神经元中 HO 诱导的 DNA 断裂焦点数量的减少相关。总之,在测试的细胞类型和同源盒蛋白数量的限制内,同源盒蛋白对氧化应激诱导的 DNA 断裂和死亡的保护作用是神经元和星形胶质细胞特有的,但没有同源盒蛋白或神经元类型特异性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/26b01287c596/enu9991930470004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/5bd89e699c05/enu9991930470001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/409824fc5dbc/enu9991930470002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/119db7015549/enu9991930470003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/26b01287c596/enu9991930470004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/5bd89e699c05/enu9991930470001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/409824fc5dbc/enu9991930470002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/119db7015549/enu9991930470003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62a5/6763833/26b01287c596/enu9991930470004.jpg

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Physiol Rev. 2018 Oct 1;98(4):1943-1982. doi: 10.1152/physrev.00018.2017.
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EMBO J. 2018 Aug 1;37(15). doi: 10.15252/embj.201797374. Epub 2018 Jun 25.
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Transcriptional elongation requires DNA break-induced signalling.转录延伸需要DNA断裂诱导的信号传导。
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Cell Rep. 2015 Oct 13;13(2):242-50. doi: 10.1016/j.celrep.2015.08.076. Epub 2015 Sep 24.
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