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半乳糖凝集素-3诱导神经发育的顶-基极性并调节脑回形成。

Galectin-3 induces neurodevelopmental apical-basal polarity and regulates gyrification.

作者信息

Soares Luana Campos, Huang Ning, Bernhardova Hana, Macarelli Viviana, Chan Marva, Nikel Lara, Bandiera Sara, Yan Dongnan, Gupta Dhanu, Cruz Elisa M, Vasaturo-Kolodner Talia, Hillis James M, Wood Matthew, Salman Mootaz, Molnár Zoltán, O'Neill Eric, Szele Francis G

机构信息

Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3QX, UK.

Kavli Institute for NanoScience Discovery, University of Oxford, Oxford, UK.

出版信息

Sci Adv. 2025 Sep 5;11(36):eadt5859. doi: 10.1126/sciadv.adt5859. Epub 2025 Sep 3.

Abstract

Apical-basal polarity (ABP) establishment and maintenance is necessary for proper brain development, yet how it is controlled is unclear. Galectin-3 (Gal-3) has been previously implicated in ABP of epithelial cells, and, here, we find that it is apically expressed in human embryonic stem cells (hESCs) during neural induction. Gal-3 blockade disrupts ABP and alters the distribution of junctional proteins in hESC-derived neural rosettes and is rescued by addition of recombinant Gal-3. Transcriptomics analysis shows that blocking Gal-3 regulates expression of genes responsible for nervous system development and cell junction assembly, among others. Last, Gal-3 blockade during embryonic development in vivo reduces horizontal cell divisions, disturbs cortical layering of neural progenitors, and induces gyrification. These data uncover a regulatory mechanism for ABP in the brain and warrant caution in modulating Gal-3 during pregnancy.

摘要

顶-基极性(ABP)的建立和维持对于正常的脑发育是必要的,但目前尚不清楚其调控机制。此前研究表明半乳糖凝集素-3(Gal-3)参与上皮细胞的ABP,在此我们发现,在神经诱导过程中,Gal-3在人类胚胎干细胞(hESC)的顶端表达。Gal-3阻断会破坏hESC来源的神经玫瑰花结中的ABP,并改变连接蛋白的分布,而添加重组Gal-3可使其恢复。转录组学分析表明,阻断Gal-3会调节负责神经系统发育和细胞连接组装等的基因表达。最后,在体内胚胎发育过程中阻断Gal-3会减少水平细胞分裂,扰乱神经祖细胞的皮质分层,并诱导脑回形成。这些数据揭示了大脑中ABP的一种调控机制,并警示在孕期调节Gal-3时需谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a70d/12407091/9183a762b675/sciadv.adt5859-f1.jpg

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