| Literature DB >> 35304896 |
Kyung-Joo Seong1, Seungho Choi1, Hyun-Gwan Lee2, Joon Haeng Rhee3, Jin Ho Lee4, Jeong-Tae Koh5, Sun-Hun Kim6, Won-Seok Choi4, Ji-Yeon Jung1, Won-Jae Kim1.
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.Entities:
Keywords: adult stem cells; animal models; cell culture; nervous system; neural differentiation; neural stem cells (NSCs); neuron
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Year: 2022 PMID: 35304896 DOI: 10.1093/stmcls/sxab025
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277