• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

少突胶质细胞分化过程中的氢化可的松诱导作用。

Hydrocortisone induction during oligodendroglial differentiation.

作者信息

Poduslo S E, Pak C H, Miller K

机构信息

Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Neurosci Lett. 1990 May 18;113(1):84-8. doi: 10.1016/0304-3940(90)90499-y.

DOI:10.1016/0304-3940(90)90499-y
PMID:1694977
Abstract

Steroid hormones are important for the normal development of brain. The addition of hydrocortisone to oligodendroglia in culture increases the level of mRNA for proteolipid protein, increases the synthesis of cerebrosides, and provides an induction of activities for the ketone body metabolizing enzymes. While proteolipid protein and cerebrosides are major components of myelin membranes, ketone bodies serve as precursors for lipid synthesis during development. Thus, hydrocortisone is important during the differentiation of oligodendroglia and during initial myelin production.

摘要

类固醇激素对大脑的正常发育至关重要。在培养的少突胶质细胞中添加氢化可的松可提高蛋白脂蛋白的mRNA水平,增加脑苷脂的合成,并诱导酮体代谢酶的活性。虽然蛋白脂蛋白和脑苷脂是髓鞘膜的主要成分,但酮体在发育过程中作为脂质合成的前体。因此,氢化可的松在少突胶质细胞分化和初始髓鞘形成过程中很重要。

相似文献

1
Hydrocortisone induction during oligodendroglial differentiation.少突胶质细胞分化过程中的氢化可的松诱导作用。
Neurosci Lett. 1990 May 18;113(1):84-8. doi: 10.1016/0304-3940(90)90499-y.
2
Induction of cerebroside synthesis in oligodendroglia.
Neurochem Res. 1990 Jul;15(7):739-42. doi: 10.1007/BF00973655.
3
Differential regulation of oligodendrocyte markers by glucocorticoids: post-transcriptional regulation of both proteolipid protein and myelin basic protein and transcriptional regulation of glycerol phosphate dehydrogenase.糖皮质激素对少突胶质细胞标志物的差异调节:蛋白脂蛋白和髓鞘碱性蛋白的转录后调节以及甘油磷酸脱氢酶的转录调节。
Proc Natl Acad Sci U S A. 1989 Sep;86(17):6807-11. doi: 10.1073/pnas.86.17.6807.
4
Induction of ketone body enzymes in glial cells.
Arch Biochem Biophys. 1989 Aug 1;272(2):318-22. doi: 10.1016/0003-9861(89)90225-7.
5
Effects of progesterone on oligodendrocyte progenitors, oligodendrocyte transcription factors, and myelin proteins following spinal cord injury.脊髓损伤后孕酮对少突胶质前体细胞、少突胶质细胞转录因子及髓鞘蛋白的影响。
Glia. 2009 Jun;57(8):884-97. doi: 10.1002/glia.20814.
6
Myelin gene expression in glia treated with oligodendroglial trophic factor.
J Neurocytol. 1995 Oct;24(10):725-34. doi: 10.1007/BF01191209.
7
Expression of a beta 1-related integrin by oligodendroglia in primary culture: evidence for a functional role in myelination.原代培养中少突胶质细胞β1相关整合素的表达:髓鞘形成中功能作用的证据
J Cell Biol. 1994 Mar;124(6):1039-46. doi: 10.1083/jcb.124.6.1039.
8
Selective expression of DM-20, an alternatively spliced myelin proteolipid protein gene product, in developing nervous system and in nonglial cells.
J Neurochem. 1992 Jun;58(6):2248-53. doi: 10.1111/j.1471-4159.1992.tb10970.x.
9
Mechanisms of myelin basic protein and proteolipid protein targeting in oligodendrocytes (review).少突胶质细胞中髓鞘碱性蛋白和蛋白脂蛋白靶向的机制(综述)
Mol Membr Biol. 1994 Apr-Jun;11(2):67-78. doi: 10.3109/09687689409162223.
10
Stabilization of myelin mRNAs as measured in a brain slice system.在脑片系统中所测定的髓磷脂mRNA的稳定性。
J Neurosci Res. 1997 Dec 15;50(6):1030-9. doi: 10.1002/(SICI)1097-4547(19971215)50:6<1030::AID-JNR14>3.0.CO;2-8.

引用本文的文献

1
Corticosteroids reverse cytokine-induced block of survival and differentiation of oligodendrocyte progenitor cells from rats.皮质类固醇可逆转细胞因子诱导的大鼠少突胶质前体细胞存活和分化的阻滞。
J Neuroinflammation. 2008 Sep 22;5:39. doi: 10.1186/1742-2094-5-39.
2
In the presence of dexamethasone, gamma interferon induces rat oligodendrocytes to express major histocompatibility complex class II molecules.在存在地塞米松的情况下,γ干扰素可诱导大鼠少突胶质细胞表达主要组织相容性复合体II类分子。
Proc Natl Acad Sci U S A. 1992 Oct 1;89(19):9054-8. doi: 10.1073/pnas.89.19.9054.