Satb2和Nr4a2是皮质层6b分化所必需的。

IF 6.1 2区 生物学 Q1 CELL BIOLOGY
Li Zhao, Yun-Chao Tao, Ling Hu, Xi-Yue Liu, Qiong Zhang, Lei Zhang, Yu-Qiang Ding, Ning-Ning Song
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引用次数: 0

摘要

皮层第6层分为两个亚层,第6b层位于白质上方,与第6a层结构不同。6b层起源于底板,包含大脑皮层发育过程中最早出生的神经元。尽管对皮层形态发生的理解已经取得了很大的进展,但关于控制6b层神经元发育的分子机制还缺乏认识。在这里,我们报道了转录因子特殊的富含at结合蛋白2 (Satb2)和核受体亚家族4组A成员2 (Nr4a2)是正常分化层6b神经元所必需的。条件缺失皮层Satb2 (Satb2Emx1 CKO)或选择性失活6b层神经元Satb2 (Satb2Nr4a2CreER CKO)后,6b层特异性基因(即Ctgf、Cplx3、Trh和Tnmd)的表达显著降低,而Nr4a2的表达显著增加,说明Satb2以细胞自主的方式参与6b层神经元的分化。另一方面,当皮层中Nr4a2缺失时,Trh和Tnmd的表达上调,而Ctgf和Cplx3的表达不变。值得注意的是,Satb2/Nr4a2双CKO小鼠中仍然存在Satb2缺失导致的分化缺陷。综上所述,我们的研究结果表明Satb2和Nr4a2都是6b层神经元分化所必需的,可能通过不同的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Satb2 and Nr4a2 are required for the differentiation of cortical layer 6b.

Cortical layer 6 is divided into two sublayers, and layer 6b is situated above the white matter with distinct architecture from layer 6a. Layer 6b arises from the subplate and contains the earliest born neurons in the development of cerebral cortex. Although great progress has been made in understanding the cortical morphogenesis, there is a dearth of knowledge regarding the molecular mechanisms governing the development of layer 6b neurons. Here we report that transcription factor special AT-rich binding protein 2 (Satb2) and nuclear receptor subfamily 4 group A member 2 (Nr4a2) are required for the normal differentiation layer 6b neurons. Upon conditional deletion of Satb2 in the cortex (Satb2Emx1 CKO) or selectively inactivation of Satb2 in layer 6b neurons only (Satb2Nr4a2CreER CKO), the expressions of layer 6b-specific genes (i.e., Ctgf, Cplx3, Trh and Tnmd) were significantly reduced, whereas that of Nr4a2 was dramatically increased, underscoring that Satb2 is involved in the differentiation of layer 6b neurons in a cell-autonomous manner. On the other hand, when Nr4a2 was deleted in the cortex, the expressions of Trh and Tnmd were upregulated with unchanged expression of Ctgf and Cplx3. Notably, the defective differentiation resulting from the deletion of Satb2 remained in Satb2/Nr4a2 double CKO mice. In summary, our findings indicated that both Satb2 and Nr4a2 are required for the differentiation of layer 6b neurons possibly via different pathways.

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来源期刊
Cell Death Discovery
Cell Death Discovery Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
8.30
自引率
1.40%
发文量
468
审稿时长
9 weeks
期刊介绍: Cell Death Discovery is a multidisciplinary, international, online-only, open access journal, dedicated to publishing research at the intersection of medicine with biochemistry, pharmacology, immunology, cell biology and cell death, provided it is scientifically sound. The unrestricted access to research findings in Cell Death Discovery will foster a dynamic and highly productive dialogue between basic scientists and clinicians, as well as researchers in industry with a focus on cancer, neurobiology and inflammation research. As an official journal of the Cell Death Differentiation Association (ADMC), Cell Death Discovery will build upon the success of Cell Death & Differentiation and Cell Death & Disease in publishing important peer-reviewed original research, timely reviews and editorial commentary. Cell Death Discovery is committed to increasing the reproducibility of research. To this end, in conjunction with its sister journals Cell Death & Differentiation and Cell Death & Disease, Cell Death Discovery provides a unique forum for scientists as well as clinicians and members of the pharmaceutical and biotechnical industry. It is committed to the rapid publication of high quality original papers that relate to these subjects, together with topical, usually solicited, reviews, editorial correspondence and occasional commentaries on controversial and scientifically informative issues.
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