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Satb2和Nr4a2是皮质6b层分化所必需的。

Satb2 and Nr4a2 are required for the differentiation of cortical layer 6b.

作者信息

Zhao Li, Tao Yun-Chao, Hu Ling, Liu Xi-Yue, Zhang Qiong, Zhang Lei, Ding Yu-Qiang, Song Ning-Ning

机构信息

Laboratory Animal Center, Fudan University, Shanghai, China.

State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai, China.

出版信息

Cell Death Discov. 2025 Mar 31;11(1):126. doi: 10.1038/s41420-025-02402-2.

Abstract

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 (Satb2 CKO) or selectively inactivation of Satb2 in layer 6b neurons only (Satb2 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.

摘要

皮层第6层分为两个亚层,6b层位于白质上方,其结构与6a层不同。6b层起源于板下带,包含大脑皮层发育中最早生成的神经元。尽管在理解皮层形态发生方面取得了很大进展,但关于调控6b层神经元发育的分子机制仍知之甚少。在此我们报告,转录因子特殊AT富集结合蛋白2(Satb2)和核受体亚家族4 A组成员2(Nr4a2)是6b层神经元正常分化所必需的。在皮层中条件性删除Satb2(Satb2 CKO)或仅在6b层神经元中选择性失活Satb2(Satb2 CKO)后,6b层特异性基因(即Ctgf、Cplx3、Trh和Tnmd)的表达显著降低,而Nr4a2的表达则显著增加,这突出表明Satb2以细胞自主方式参与6b层神经元的分化。另一方面,当在皮层中删除Nr4a2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缺失导致的分化缺陷在Satb2/Nr4a2双基因敲除小鼠中仍然存在。总之,我们的研究结果表明,Satb2和Nr4a2可能通过不同途径参与6b层神经元的分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b03/11958660/27ebc6ec96e4/41420_2025_2402_Fig1_HTML.jpg

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