科研成果详情

题名RBP-J deficiency promoted the proliferation and differentiation of CD133-positive cells in both in vitro and in vivo studies
作者
发表日期2022-07
发表期刊EUROPEAN JOURNAL OF NEUROSCIENCE   影响因子和分区
语种英语
原始文献类型Article ; Early Access
关键词CD133-positive cell cell proliferation and differentiation neural stem cell notch signalling pathway RBP-J
其他关键词NEURAL STEM-CELLS ; CENTRAL-NERVOUS-SYSTEM ; SUBVENTRICULAR ZONE ASTROCYTES ; SPINAL-CORD-INJURY ; EPENDYMAL CELLS ; DOPAMINERGIC-NEURONS ; SUBSTANTIA-NIGRA ; PROGENITOR CELLS ; STEM/PROGENITOR CELLS ; SELF-RENEWAL
摘要Although Notch signalling pathway could control the proliferation and differentiation of neural stem cells (NSCs), it is largely unknown about the effect of Notch signalling pathway on the neurogenesis of CD133-positive cells. By using the primary cultured ependymal cells and the transgenic mouse, we found that CD133 immunoreactivity was exclusively localized in the ependymal layer of ventricles; moreover, most CD133-positive cells were co-labelled with Nestin. In addition, recombination signal binding protein J (RBP-J), a key nuclear effector of Notch signalling pathway, was highly active in CD133-positive cells. CD133-positive cells can differentiate into the immature and mature neurons; in particular, the number of CD133-positive cells differentiating into the immature and mature neurons was significantly increased following the deficiency or interference of RBP-J in vivo or in vitro. By using real-time qPCR and Western blot, we found that RBP-J and Hes1 were downregulated, whereas Notch1 was upregulated in the expression levels of mRNAs and proteins following the deficiency or interference of RBP-J. These results demonstrated RBP-J deficiency promoted the proliferation and differentiation of CD133-positive cells. Therefore, we speculated that RBP-J could maintain CD133-positive cells in the characteristics of NSCs possibly by regulating Notch1/RBP-J/Hes1 pathway. It will provide a novel molecular insight into the function of RBP-J as well as facilitate a future investigation of CD133-positive cells with respect to their potential application in neurodegenerative disorder.
资助项目Wenzhou Public Welfare Science and Technology Project of China [Y20190059]; Zhejiang Provincial Natural Science Foundation of China [LY22H090004]; National Natural Science Foundation of China [81671401, 82171577]
出版者WILEY
出版地HOBOKEN
ISSN0953-816X
EISSN1460-9568
卷号56期号:2页码:3839-3860
DOI10.1111/ejn.15727
页数22
WOS类目Neurosciences
WOS研究方向Neurosciences & Neurology
WOS记录号WOS:000810572000001
收录类别SCIE ; SCOPUS ; PUBMED
URL查看原文
PubMed ID35661443
SCOPUSEID2-s2.0-85131749483
通讯作者地址[Sun, Chenyou]Department of Anatomy,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,China ; [Liao, Min]Institute of Neuroscience,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,China
Scopus学科分类Neuroscience (all)
引用统计
被引频次[WOS]:0   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符https://kms.wmu.edu.cn/handle/3ETUA0LF/148395
专题基础医学院(机能实验教学中心)
基础医学院(机能实验教学中心)_形态学系_组织胚胎学
通讯作者Liao, Min; Sun, Chenyou
作者单位
1.Department of Anatomy,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,China;
2.Institute of Neuroscience,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,China;
3.Department of Histology and Embryology,School of Basic Medical Sciences,Wenzhou Medical University,Wenzhou,China
第一作者单位基础医学院(机能实验教学中心)
通讯作者单位基础医学院(机能实验教学中心)
第一作者的第一单位基础医学院(机能实验教学中心)
推荐引用方式
GB/T 7714
Ye, Xin,Li, Mengyi,Bian, Wei,et al. RBP-J deficiency promoted the proliferation and differentiation of CD133-positive cells in both in vitro and in vivo studies[J]. EUROPEAN JOURNAL OF NEUROSCIENCE,2022,56(2):3839-3860.
APA Ye, Xin., Li, Mengyi., Bian, Wei., Wu, Anting., Zhang, Ting., ... & Sun, Chenyou. (2022). RBP-J deficiency promoted the proliferation and differentiation of CD133-positive cells in both in vitro and in vivo studies. EUROPEAN JOURNAL OF NEUROSCIENCE, 56(2), 3839-3860.
MLA Ye, Xin,et al."RBP-J deficiency promoted the proliferation and differentiation of CD133-positive cells in both in vitro and in vivo studies".EUROPEAN JOURNAL OF NEUROSCIENCE 56.2(2022):3839-3860.

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