Multiple functions of Hes genes in the proliferation and differentiation of neural stem cells

Aquila, 2020, Ticagrelor increases sirt1 and hes1 mrna levels in peripheral blood cells from patients with stable coronary artery disease and chronic obstructive pulmonary disease, Int. J. Mol. Sci., 21, 1576, 10.3390/ijms21051576 Bai, 2007, Id sustains hes1 expression to inhibit precocious neurogenesis by releasing negative autoregulation of hes1, Dev. Cell, 13, 283, 10.1016/j.devcel.2007.05.014 Baik, 2020, Intermittent fasting increases adult hippocampal neurogenesis, Brain Behav., 10, 10.1002/brb3.1444 Bansod, 2017, Hes5 regulates the transition timing of neurogenesis and gliogenesis in mammalian neocortical development, Development, 144, 3156, 10.1242/dev.147256 Baxi, 2017, Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone-induced demyelination, Glia, 65, 2087, 10.1002/glia.23229 Biga, 2021, A dynamic, spatially periodic, micro-pattern of hes5 underlies neurogenesis in the mouse spinal cord, Mol. Syst. Biol., 17, 10.15252/msb.20209902 Boareto, 2020, Patterning via local cell-cell interactions in developing systems, Dev. Biol., 460, 77, 10.1016/j.ydbio.2019.12.008 Boareto, 2017, Differential interactions between notch and id factors control neurogenesis by modulating hes factor autoregulation, Development, 144, 3465, 10.1242/dev.152520 Bosze, 2020, Simultaneous requirements for hes1 in retinal neurogenesis and optic cup-stalk boundary maintenance, J. Neurosci., 40, 1501, 10.1523/JNEUROSCI.2327-19.2020 Buscarlet, 2008, Inhibition of cortical neuron differentiation by groucho/tle1 requires interaction with wrpw, but not eh1, repressor peptides, J. Biol. Chem., 283, 24881, 10.1074/jbc.M800722200 Chen, 2015, Neurofibromatosis-1 regulation of neural stem cell proliferation and multilineage differentiation operates through distinct ras effector pathways, Genes Dev., 29, 1677, 10.1101/gad.261677.115 Cheng, 2020, Reactive astrocytes display pro-inflammatory adaptability with modulation of notch-pi3k-akt signaling pathway under inflammatory stimulation, Neuroscience, 440, 130, 10.1016/j.neuroscience.2020.05.023 Contreras, 2018, Dynamic notch signalling regulates neural stem cell state progression in the drosophila optic lobe, Neural Dev., 13, 25, 10.1186/s13064-018-0123-8 De Decker, 2020, Hes1 and hes4 have non-redundant roles downstream of notch during early human t cell development, Haematologica, 106, 130, 10.3324/haematol.2019.226126 Dhanesh, 2016, Hes1: the maestro in neurogenesis, Cell Mol. Life Sci., 73, 4019, 10.1007/s00018-016-2277-z Engler, 2018, Notch and neurogenesis, Adv. Exp. Med. Biol., 1066, 223, 10.1007/978-3-319-89512-3_11 Eun, 2010, Induction of neuronal apoptosis by expression of hes6 via p53-dependent pathway, Brain Res., 1313, 1, 10.1016/j.brainres.2009.11.078 Fan, 2018, Effect of notch1 gene on remyelination in multiple sclerosis in mouse models of acute demyelination, J. Cell Biochem., 119, 9284, 10.1002/jcb.27197 Fischer, 2002, Hey bhlh factors in cardiovascular development, Cold Spring Harb. Symp. Quant. Biol., 67, 63, 10.1101/sqb.2002.67.63 Ge, 2019, Stage-dependent regulation of oligodendrocyte development and enhancement of myelin repair by dominant negative master-mind 1 protein, Glia, 67, 1654, 10.1002/glia.23633 Hatakeyama, 2004, Hes genes regulate size, shape and histogenesis of the nervous system by control of the timing of neural stem cell differentiation, Development, 131, 5539, 10.1242/dev.01436 He, 2013, Coordinated control of oligodendrocyte development by extrinsic and intrinsic signaling cues, Neurosci. Bull., 29, 129, 10.1007/s12264-013-1318-y Hong, 2018, The b-hlh transcription factor hes3 participates in neural plate border formation by interfering with wnt/β-catenin signaling, Dev. Biol., 442, 162, 10.1016/j.ydbio.2018.07.011 Huang, 2013, Regulation of the timing of oligodendrocyte differentiation: mechanisms and perspectives, Neurosci. Bull., 29, 155, 10.1007/s12264-013-1314-2 Imayoshi, 2013, Oscillatory control of factors determining multipotency and fate in mouse neural progenitors, Science, 342, 1203, 10.1126/science.1242366 Iso, 2003, Hes and herp families: multiple effectors of the notch signaling pathway, J. Cell Physiol., 194, 237, 10.1002/jcp.10208 Jhas, 2006, Hes6 inhibits astrocyte differentiation and promotes neurogenesis through different mechanisms, J. Neurosci., 26, 11061, 10.1523/JNEUROSCI.1358-06.2006 Kageyama, 2015, Dynamic expression and roles of hes factors in neural development, Cell Tissue Res., 359, 125, 10.1007/s00441-014-1888-7 Kageyama, 2018, Oscillatory control of notch signaling in development, Adv. Exp. Med. Biol., 1066, 265, 10.1007/978-3-319-89512-3_13 Kageyama, 2019, Dynamic control of neural stem cells by bhlh factors, Neurosci. Res., 138, 12, 10.1016/j.neures.2018.09.005 Kobayashi, 2015, Deubiquitinating enzymes regulate hes1 stability and neuronal differentiation, FEBS J., 282, 2411, 10.1111/febs.13290 Kobayashi, 2014, Expression dynamics and functions of hes factors in development and diseases, Curr. Top. Dev. Biol., 110, 263, 10.1016/B978-0-12-405943-6.00007-5 Kuwabara, 2009, Wnt-mediated activation of neurod1 and retro-elements during adult neurogenesis, Nat. Neurosci., 12, 1097, 10.1038/nn.2360 Lee, 2012, Circadian regulation of low density lipoprotein receptor promoter activity by clock/bmal1, hes1 and hes6, Exp. Mol. Med., 44, 642, 10.3858/emm.2012.44.11.073 Li, 2020, Wnt4-modified nsc transplantation promotes functional recovery after spinal cord injury, FASEB J., 34, 82, 10.1096/fj.201901478RR Lin, 2017, Kdm3a-mediated demethylation of histone h3 lysine 9 facilitates the chromatin binding of neurog2 during neurogenesis, Development, 144, 3674, 10.1242/dev.144113 Majumder, 2021, Targeting notch in oncology: the path forward, Nat. Rev. Drug Discov., 20, 125, 10.1038/s41573-020-00091-3 Manning, 2019, Quantitative single-cell live imaging links hes5 dynamics with cell-state and fate in murine neurogenesis, Nat. Commun., 10, 2835, 10.1038/s41467-019-10734-8 Marquez-Curtis, 2021, Cryopreservation of human cerebral microvascular endothelial cells and astrocytes in suspension and monolayers, PLoS One, 16, 10.1371/journal.pone.0249814 Massari, 2000, Helix-loop-helix proteins: regulators of transcription in eucaryotic organisms, Mol. Cell Biol., 20, 429, 10.1128/MCB.20.2.429-440.2000 Murai, 2011, Hes6 is required for the neurogenic activity of neurogenin and neurod, PLoS One, 6, 10.1371/journal.pone.0027880 Nakazaki, 2008, Key basic helix-loop-helix transcription factor genes hes1 and ngn2 are regulated by pax3 during mouse embryonic development, Dev. Biol., 316, 510, 10.1016/j.ydbio.2008.01.008 Nam, 2016, Hairy and enhancer of split 6 (hes6) deficiency in mouse impairs neuroblast differentiation in dentate gyrus without affecting cell proliferation and integration into mature neurons, Cell Mol. Neurobiol., 36, 57, 10.1007/s10571-015-0220-8 Nikolakopoulou, 2016, Stat3-ser/hes3 signaling: A new molecular component of the neuroendocrine system, Horm. Metab. Res., 48, 77, 10.1055/s-0041-111699 Ochi, 2020, Oscillatory expression of hes1 regulates cell proliferation and neuronal differentiation in the embryonic brain, Development, 147 Ohtsuka, 2021, Hes1 overexpression leads to expansion of embryonic neural stem cell pool and stem cell reservoir in the postnatal brain, Development, 148, 10.1242/dev.189191 Ohtsuka, 2001, Roles of the basic helix-loop-helix genes hes1 and hes5 in expansion of neural stem cells of the developing brain, J. Biol. Chem., 276, 30467, 10.1074/jbc.M102420200 Peng, 2019, Inhibition of notch1 signaling promotes neuronal differentiation and improves functional recovery in spinal cord injury through suppressing the activation of ras homolog family member a, J. Neurochem, 150, 709, 10.1111/jnc.14833 Pilz, 2018, Live imaging of neurogenesis in the adult mouse hippocampus, Science, 359, 658, 10.1126/science.aao5056 Rabadán, 2012, Jagged2 controls the generation of motor neuron and oligodendrocyte progenitors in the ventral spinal cord, Cell Death Differ., 19, 209, 10.1038/cdd.2011.84 Reiman, 2020, Consensus recommendations on the classification, definition and diagnostic criteria of hip-related pain in young and middle-aged active adults from the international hip-related pain research network, zurich 2018, Br. J. Sports Med., 54, 631, 10.1136/bjsports-2019-101453 Roese-Koerner, 2017, Notch/hes signaling and mir-9 engage in complex feedback interactions controlling neural progenitor cell proliferation and differentiation, Neurogenesis (Austin), 4 Rowitch, 2010, Developmental genetics of vertebrate glial-cell specification, Nature, 468, 214, 10.1038/nature09611 Sengupta, 2018, Alteration in microrna expression governs the nature and timing of cellular fate commitment, ACS Chem. Neurosci., 9, 725, 10.1021/acschemneuro.7b00423 Shi, 2015, Mir-381 regulates neural stem cell proliferation and differentiation via regulating hes1 expression, PLoS One, 10, 10.1371/journal.pone.0138973 Shimojo, 2008, Oscillations in notch signaling regulate maintenance of neural progenitors, Neuron, 58, 52, 10.1016/j.neuron.2008.02.014 Singh, 2020, Molecular crosstalk: notch can manipulate hes1 and mir-9 behavior, J. Theor. Biol., 504, 10.1016/j.jtbi.2020.110404 Smyth, 2019, Seminars in cell and developmental biology, Semin Cell Dev. Biol., 91, 84, 10.1016/j.semcdb.2018.11.003 Sueda, 2019, High hes1 expression and resultant ascl1 suppression regulate quiescent vs. active neural stem cells in the adult mouse brain, Genes Dev., 33, 511, 10.1101/gad.323196.118 Toutouna, 2016, Hes3 expression in the adult mouse brain is regulated during demyelination and remyelination, Brain Res., 1642, 124, 10.1016/j.brainres.2016.03.014 Vilas-Boas, 2010, Hes6-1 and hes6-2 function through different mechanisms during neuronal differentiation, PLoS One, 5, 10.1371/journal.pone.0015459 Wu, 2016, Gamma-secretase inhibitor prevents proliferation and migration of ductus arteriosus smooth muscle cells through the notch3-hes1/2/5 pathway, Int. J. Biol. Sci., 12, 1063, 10.7150/ijbs.16430 Xiao, 2020, Differential inhibition of sox10 functions by notch-hes pathway, Cell Mol. Neurobiol., 40, 653, 10.1007/s10571-019-00764-7 Zhang, 2011, Role of transcription factors in neurogenesis after cerebral ischemia, Rev. Neurosci., 22, 457, 10.1515/rns.2011.034 Zhang, 2018, Notch: an interactive player in neurogenesis and disease, Cell Tissue Res., 371, 73, 10.1007/s00441-017-2641-9 Zhang, 2015, Notch-1 signaling regulates astrocytic proliferation and activation after hypoxia exposure, Neurosci. Lett., 603, 12, 10.1016/j.neulet.2015.07.009 Zhu, 2014, Genetic evidence that nkx2.2 and pdgfra are major determinants of the timing of oligodendrocyte differentiation in the developing cns, Development, 141, 548, 10.1242/dev.095323