• 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

Cell lineage analysis of Schwann cells in the PNS determined by shiverer-normal mouse chimeras.

作者信息

Mikoshiba K, Yokoyama M, Takamatsu K, Tsukada Y, Nomura T

出版信息

Dev Biol. 1984 Sep;105(1):221-6. doi: 10.1016/0012-1606(84)90277-x.

DOI:10.1016/0012-1606(84)90277-x
PMID:6205920
Abstract

The myelin of the peripheral nervous system from the shiverer mutant mice is characterized by the absence of myelin basic protein, while the other myelin protein components are present at normal levels. Myelin lamella formation is normal in the shiverer mutant. Therefore, by using antiserum against myelin basic protein, we can distinguish the shiverer from the wild-type control myelin immunohistochemically. To study the cell lineage of Schwann cells, chimeras produced by the aggregation of eight-cell embryos from wild-type mice and shiverer mice have been used. Using myelin basic protein as a marker, it was observed that Schwann cells in the sciatic nerve existed as patches of cells with like-genotype. The patches occurred in a linear array along the axons with some intermingling of Schwann cells. Complete randomization by intermingling of Schwann cells was not observed and clones of Schwann cells may persist as contiguous groups throughout peripheral nerve development.

摘要

相似文献

1
Cell lineage analysis of Schwann cells in the PNS determined by shiverer-normal mouse chimeras.
Dev Biol. 1984 Sep;105(1):221-6. doi: 10.1016/0012-1606(84)90277-x.
2
P1 deficiency in shiverer myelin is expressed by Schwann cells in shiverer dystrophic normal mouse chimaera nerves.在颤抖性营养不良正常小鼠嵌合神经中,施万细胞表达了颤抖性髓磷脂中的P1缺乏。
Neurosci Lett. 1983 Jul 29;38(2):163-8. doi: 10.1016/0304-3940(83)90034-4.
3
Hypomyelination in the peripheral nervous system of shiverer mice and in shiverer in equilibrium normal chimaera.颤抖小鼠外周神经系统以及平衡正常嵌合体中颤抖小鼠的髓鞘形成不足。
J Comp Neurol. 1984 Aug 10;227(3):348-56. doi: 10.1002/cne.902270305.
4
Peripheral nervous system of shiverer mutant mice: developmental change of myelin components and immunohistochemical demonstration of the absence of MBP and presence of P2 protein.颤抖突变小鼠的外周神经系统:髓鞘成分的发育变化以及髓磷脂碱性蛋白缺失和P2蛋白存在的免疫组织化学证明
Brain Res. 1983 Mar;283(1):71-9. doi: 10.1016/0165-3806(83)90082-2.
5
Neurochemical and morphological studies on the myelin of peripheral nervous system from Shiverer mutant mice: absence of basic proteins common to central nervous system.颤抖突变小鼠外周神经系统髓鞘的神经化学和形态学研究:缺乏中枢神经系统共有的碱性蛋白。
Brain Res. 1981 Jan 12;204(2):455-60. doi: 10.1016/0006-8993(81)90608-9.
6
Immunoreactive myelin basic proteins are not detected when shiverer mutant Schwann cells and fibroblasts are co-cultured with normal neurons.当颤抖突变型雪旺细胞和成纤维细胞与正常神经元共培养时,未检测到免疫反应性髓鞘碱性蛋白。
J Cell Biol. 1984 Apr;98(4):1291-5. doi: 10.1083/jcb.98.4.1291.
7
Chimeric analysis of the pathogenesis of dysmyelination of shiverer mutant mice. Presence of patches of MBP-positive and negative sites in white matter indicating the absence of humoral factors for dysmyelination.颤抖突变小鼠脱髓鞘发病机制的嵌合体分析。白质中存在髓鞘碱性蛋白(MBP)阳性和阴性区域,表明脱髓鞘不存在体液因素。
Dev Neurosci. 1982;5(5-6):520-4. doi: 10.1159/000112713.
8
Normal basal laminas are realized on dystrophic Schwann cells in dystrophic in equilibrium shiverer chimera nerves.在营养不良性平衡型颤抖嵌合体神经中,正常的基底膜在营养不良性施万细胞上得以实现。
J Cell Biol. 1984 Nov;99(5):1831-7. doi: 10.1083/jcb.99.5.1831.
9
Normal rate of Schwann cell proliferation in the MBP-deficient shiverer mouse during Wallerian degeneration.
Brain Res. 1991 Nov 1;563(1-2):345-8. doi: 10.1016/0006-8993(91)91560-n.
10
A mitogen for Schwann cells is derived from myelin basic protein.一种施万细胞促分裂原源自髓鞘碱性蛋白。
Biochem Biophys Res Commun. 1989 Oct 31;164(2):883-8. doi: 10.1016/0006-291x(89)91541-6.