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

被引:0
作者
Zhao, Li [1 ,2 ,3 ]
Tao, Yun-Chao [2 ,3 ]
Hu, Ling [1 ]
Liu, Xi-Yue [2 ,3 ]
Zhang, Qiong [1 ]
Zhang, Lei [4 ,5 ]
Ding, Yu-Qiang [1 ,2 ,3 ,6 ,7 ]
Song, Ning-Ning [1 ]
机构
[1] Fudan Univ, Lab Anim Ctr, Shanghai 200032, Peoples R China
[2] Fudan Univ, Inst Brain Sci, MOE Frontiers Ctr Brain Sci, Shanghai, Peoples R China
[3] Fudan Univ, Inst Brain Sci, MOE Frontiers Ctr Brain Sci, Shanghai, Peoples R China
[4] Tongji Univ, Sch Med, Shanghai Yangzhi Rehabil Hosp, Shanghai Sunshine Rehabil Ctr, Shanghai, Peoples R China
[5] Tongji Univ, Clin Ctr Brain & Spinal Cord Res, Shanghai, Peoples R China
[6] Fudan Univ, Shanghai Inst Infect Dis & Biosecur, Shanghai, Peoples R China
[7] Fudan Univ, Huashan Hosp, Huashan Inst Med HS IOM, Shanghai 200040, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
TRANSCRIPTION FACTOR SATB2; EXCITATORY NEURONS; SUBPLATE; EXPRESSION; GENE; DETERMINANT; CALLOSAL;
D O I
10.1038/s41420-025-02402-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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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页数:9
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