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癌基因 Mycn 在成体神经发生和少突胶质细胞发生中的功能。

Function of Oncogene Mycn in Adult Neurogenesis and Oligodendrogenesis.

机构信息

Department of Anesthesia and Perioperative Care, University of California San Francisco, San Francisco, CA, 94143, USA.

出版信息

Mol Neurobiol. 2022 Jan;59(1):77-92. doi: 10.1007/s12035-021-02584-7. Epub 2021 Oct 8.

Abstract

Human MYCN is an oncogene amplified in neuroblastoma and many other tumors. Both human MYCN and mouse Mycn genes are important in embryonic brain development, but their functions in adult healthy nerve system are completely unknown. Here, with Mycn-eGFP mice and quantitative RT-PCR, we found that Mycn was expressed in specific brain regions of young adult mice, including subventricular zone (SVZ), subgranular zone (SGZ), olfactory bulb (OB), subcallosal zone (SCZ), and corpus callosum (CC). With immunohistochemistry (IHC), we found that many Mycn-expressing cells expressed neuroblast marker doublecortin (DCX) and proliferation marker Ki67. With Dcx-creER and Mki67-creER mouse lines, we fate mapped Dcx-expressing neuroblasts and Mki67-expressing proliferation cells, along with deleting Mycn from these cells in adult mice. We found that knocking out Mycn from adult neuroblasts or proliferating cells significantly reduced cells in proliferation in SVZ, SGZ, OB, SCZ, and CC. We also demonstrated that the Mycn-deficient neuroblasts in SGZ matured quicker than wild-type neuroblasts, and that Mycn-deficient proliferating cells were more likely to survive in SVZ, SGZ, OB, SCZ, and CC compared to wild type. Thus, our results demonstrate that, in addition to causing tumors in the nervous system, oncogene Mycn has a crucial function in neurogenesis and oligodendrogenesis in adult healthy brain.

摘要

人类 MYCN 是神经母细胞瘤和许多其他肿瘤中扩增的癌基因。人类 MYCN 和小鼠 Mycn 基因在胚胎大脑发育中都很重要,但它们在成年健康神经系统中的功能完全未知。在这里,我们使用 Mycn-eGFP 小鼠和定量 RT-PCR 发现,Mycn 在年轻成年小鼠的特定脑区表达,包括侧脑室下区(SVZ)、颗粒下区(SGZ)、嗅球(OB)、胼胝体下区(SCZ)和胼胝体(CC)。通过免疫组织化学(IHC),我们发现许多表达 Mycn 的细胞表达神经母细胞标志物双皮质素(DCX)和增殖标志物 Ki67。使用 Dcx-creER 和 Mki67-creER 小鼠系,我们对 Dcx 表达的神经前体细胞和 Mki67 表达的增殖细胞进行了命运映射,并在成年小鼠中从这些细胞中敲除了 Mycn。我们发现,在成年神经前体细胞或增殖细胞中敲除 Mycn 会显著减少 SVZ、SGZ、OB、SCZ 和 CC 中的增殖细胞。我们还证明,SGZ 中缺乏 Mycn 的神经前体细胞比野生型神经前体细胞成熟得更快,并且与野生型相比,SVZ、SGZ、OB、SCZ 和 CC 中的缺乏 Mycn 的增殖细胞更有可能存活。因此,我们的结果表明,除了在神经系统中引起肿瘤外,癌基因 Mycn 在成年健康大脑的神经发生和少突胶质细胞发生中具有关键功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/daaa/8786763/83ff23e73ea8/12035_2021_2584_Fig1_HTML.jpg

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