• 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

新生大鼠脑内X射线诱导凋亡后的阿米巴样小胶质细胞反应。

Amoeboid microglial response following X-ray-induced apoptosis in the neonatal rat brain.

作者信息

Ferrer I, Olivé M, Blanco R, Ballabriga J, Cinós C, Planas A M

机构信息

Unitat de Neuropatologia, Hospital Prínceps d'Espanya, Universitat de Barcelona, Spain.

出版信息

Neurosci Lett. 1995 Jun 30;193(2):109-12. doi: 10.1016/0304-3940(95)11679-q.

DOI:10.1016/0304-3940(95)11679-q
PMID:7478153
Abstract

The phagocytic response following X-ray-induced apoptosis in the neonatal rat brain was examined by immunohistochemistry with the antibodies OX-6 and OX-42 which recognize MHC class II antigens and the CR3 complement receptor, respectively. Few OX-6-immunoreactive cells were observed in control rats, and in rats irradiated at postnatal day 2 and examined during the first 2 postnatal weeks. However, a transient increase in the number of OX-42-immunoreactive amoeboid microglia, containing large numbers of apoptotic cells, occurred at 6, 24 and 48 h after irradiation when compared with age-matched controls. These results show that X-ray-induced apoptosis promotes a short-lasting phagocytic response.

摘要

通过分别使用识别MHC II类抗原的抗体OX-6和识别CR3补体受体的抗体OX-42进行免疫组织化学,研究了新生大鼠脑内X射线诱导凋亡后的吞噬反应。在对照大鼠以及出生后第2天接受照射并在出生后前2周内进行检查的大鼠中,很少观察到OX-6免疫反应性细胞。然而,与年龄匹配的对照相比,照射后6、24和48小时出现了OX-42免疫反应性阿米巴样小胶质细胞数量的短暂增加,这些细胞含有大量凋亡细胞。这些结果表明,X射线诱导的凋亡促进了短暂的吞噬反应。

相似文献

1
Amoeboid microglial response following X-ray-induced apoptosis in the neonatal rat brain.新生大鼠脑内X射线诱导凋亡后的阿米巴样小胶质细胞反应。
Neurosci Lett. 1995 Jun 30;193(2):109-12. doi: 10.1016/0304-3940(95)11679-q.
2
Upregulation and induction of surface antigens with special reference to MHC class II expression in microglia in postnatal rat brain following intravenous or intraperitoneal injections of lipopolysaccharide.静脉或腹腔注射脂多糖后,新生大鼠脑内小胶质细胞表面抗原的上调与诱导,特别涉及MHC II类分子的表达
J Anat. 1994 Apr;184 ( Pt 2)(Pt 2):285-96.
3
Response of amoeboid microglia/brain macrophages in fetal rat brain exposed to a teratogen.
J Neurosci Res. 2001 Apr 1;64(1):79-93. doi: 10.1002/jnr.1056.
4
Effects of colchicine on amoeboid microglial cells in the postnatal rat brain.
Arch Histol Cytol. 1997 Dec;60(5):453-62. doi: 10.1679/aohc.60.453.
5
Transient expression of osteopontin mRNA and protein in amoeboid microglia in developing rat brain.
Exp Brain Res. 2004 Feb;154(3):275-80. doi: 10.1007/s00221-003-1657-4. Epub 2003 Oct 14.
6
Effects of melatonin on macrophages/microglia in postnatal rat brain.褪黑素对新生大鼠大脑中巨噬细胞/小胶质细胞的影响。
J Pineal Res. 1999 Apr;26(3):158-68. doi: 10.1111/j.1600-079x.1999.tb00578.x.
7
Expression of major histocompatibility complex and leukocyte common antigens in amoeboid microglia in postnatal rats.主要组织相容性复合体和白细胞共同抗原在新生大鼠阿米巴样小胶质细胞中的表达。
J Anat. 1991 Aug;177:117-26.
8
Expression and distribution of various antigens of developing microglial cells in the rat telencephalon.大鼠端脑中发育中小胶质细胞各种抗原的表达与分布
J Hirnforsch. 1999;39(3):283-91.
9
Immunohistochemical study of microglial and astroglial cells during postnatal development of rat striatum.
Folia Morphol (Warsz). 2000;58(4):315-23.
10
Response of amoeboid microglial cells to chloroquine injections in postnatal rats.产后大鼠中阿米巴样小胶质细胞对氯喹注射的反应。
J Hirnforsch. 1996;37(2):233-42.

引用本文的文献

1
Single-cell microglial transcriptomics during demyelination defines a microglial state required for lytic carcass clearance.单细胞小胶质细胞在脱髓鞘过程中的转录组学定义了一种小胶质细胞状态,该状态对于裂解残骸的清除是必需的。
Mol Neurodegener. 2022 Dec 13;17(1):82. doi: 10.1186/s13024-022-00584-2.
2
Null mutation of c-fos causes exacerbation of methamphetamine-induced neurotoxicity.c-fos基因的无效突变会加剧甲基苯丙胺诱导的神经毒性。
J Neurosci. 1999 Nov 15;19(22):10107-15. doi: 10.1523/JNEUROSCI.19-22-10107.1999.