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Toll 样受体 5 促进小鼠胚胎干细胞和成年海马神经干细胞的神经发生。

Toll-Like Receptor 5 Promotes the Neurogenesis From Embryonic Stem Cells and Adult Hippocampal Neural Stem Cells in Mice.

机构信息

Dental Science Research Institute, Hard-tissue Biointerface Research Center, Department of Oral Physiology, School of Dentistry, Chonnam National University, Gwangju, Republic of Korea.

Department of Oceanography, Marine Ecological Disturbing and Harmful Organisms Research Center, BK21+ Climate Change and Coastal Ecosystem Prediction Research Center, Chonnam National University, Gwangju, Republic of Korea.

出版信息

Stem Cells. 2022 Mar 31;40(3):303-317. doi: 10.1093/stmcls/sxab025.

Abstract

Toll-like receptors (TLRs) make a crucial contribution to the innate immune response. TLR5 was expressed in embryoid body derived from mouse embryonic stem cells (mESCs) and βIII-tubulin-positive cells under all-trans retinoic acid-treated condition. TLR5 was upregulated during neural differentiation from mESCs and augmented the neural differentiation of mESCs via nuclear factor-κB and interleukin 6/CREB pathways. Besides, TLR5 was expressed in SOX2- or doublecortin-positive cells in the subgranular zone of the hippocampal dentate gyrus where adult neurogenesis occurs. TLR5 inhibited the proliferation of adult hippocampal neural stem cells (NSCs) by regulating the cell cycle and facilitated the neural differentiation from the adult hippocampal NSCs via JNK pathway. Also, TLR5 deficiency impaired fear memory performance in mice. Our data suggest that TLR5 is a crucial modulator of neurogenesis from mESCs and adult hippocampal NSCs in mice and represents a new therapeutic target in neurological disorders related to cognitive function.

摘要

Toll 样受体 (TLRs) 对先天免疫反应起着至关重要的作用。TLR5 在胚状体中表达,胚状体来源于经全反式视黄酸处理的小鼠胚胎干细胞 (mESCs) 和 βIII-微管蛋白阳性细胞。TLR5 在 mESCs 的神经分化过程中上调,并通过核因子-κB 和白细胞介素 6/CREB 途径增强 mESCs 的神经分化。此外,TLR5 表达于海马齿状回颗粒下区的 SOX2 或双皮质素阳性细胞中,而成年神经发生发生在此处。TLR5 通过调节细胞周期抑制成年海马神经干细胞 (NSCs) 的增殖,并通过 JNK 途径促进成年海马 NSCs 的神经分化。此外,TLR5 缺乏会损害小鼠的恐惧记忆表现。我们的数据表明,TLR5 是小鼠 mESCs 和成年海马 NSCs 神经发生的关键调节因子,是与认知功能相关的神经紊乱的新治疗靶点。

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