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Telomerase reverse transcriptase (TERT)-expressing cells mark a novel stem cell population in the adult mouse brain

https://doi.org/10.1101/2023.02.09.527879

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/(sici)1520-6408(1996)18:2<173::aid-dvg10>3.0.co;2-3openalex-snapshot

Telomerase activity in human germline and embryonic tissues and cells

inferredcites →https://doi.org/10.1002/9780470151808.sc05a02s36openalex-snapshot

Identifying Adult Stem Cells Using Cre‐Mediated Lineage Tracing

inferredcites →https://doi.org/10.1002/cne.21492openalex-snapshot

Evidence for constitutive neural cell proliferation in the adult murine hypothalamus

inferredcites →https://doi.org/10.1002/dvg.20335openalex-snapshot

A global double‐fluorescent Cre reporter mouse

inferredcites →https://doi.org/10.1002/glia.20255openalex-snapshot

Choroid plexus ependymal cells host neural progenitor cells in the rat

inferredcites →https://doi.org/10.1002/jnr.1073openalex-snapshot

Differential regulation of telomerase activity and TERT expression during brain development in mice

inferredcites →https://doi.org/10.1002/stem.2706openalex-snapshot

Bone Marrow Stem Cells Do Not Contribute to Endometrial Cell Lineages in Chimeric Mouse Models

inferredcites →https://doi.org/10.1002/stem.3318openalex-snapshot

Telomerase expression marks transitional growth-associated skeletal progenitor/stem cells

inferredcites →https://doi.org/10.1006/bbrc.1996.1054openalex-snapshot

Telomere Reduction and Telomerase Inactivation during Neuronal Cell Differentiation

inferredcites →https://doi.org/10.1007/s10735-007-9114-5openalex-snapshot

The how and why of adult neurogenesis

inferredcites →https://doi.org/10.1007/s11033-016-4065-0openalex-snapshot

The cell fate: senescence or quiescence

inferredcites →https://doi.org/10.1016/b978-0-12-804279-3.00002-2openalex-snapshot

The cerebrospinal fluid and barriers – anatomic and physiologic considerations

inferredcites →https://doi.org/10.1016/j.bbr.2019.112458openalex-snapshot

Adult neurogenesis, human after all (again): Classic, optimized, and future approaches

inferredcites →https://doi.org/10.1016/j.cell.2004.05.013openalex-snapshot

Axon Guidance of Mouse Olfactory Sensory Neurons by Odorant Receptors and the β2 Adrenergic Receptor

inferredcites →https://doi.org/10.1016/j.cell.2014.01.044openalex-snapshot

Neurogenesis in the Striatum of the Adult Human Brain

inferredcites →https://doi.org/10.1016/j.cell.2014.10.010openalex-snapshot

iDISCO: A Simple, Rapid Method to Immunolabel Large Tissue Samples for Volume Imaging

inferredcites →https://doi.org/10.1016/j.metabol.2021.154837openalex-snapshot

Bone morphogenetic proteins (BMPs) in the central regulation of energy balance and adult neural plasticity

inferredcites →https://doi.org/10.1016/j.neuron.2011.05.001openalex-snapshot

Adult Neurogenesis in the Mammalian Brain: Significant Answers and Significant Questions

inferredcites →https://doi.org/10.1016/j.scr.2013.06.006openalex-snapshot

Cortical lesion stimulates adult subventricular zone neural progenitor cell proliferation and migration to the site of injury

inferredcites →https://doi.org/10.1016/j.stem.2010.03.017openalex-snapshot

Quiescent and Active Hippocampal Neural Stem Cells with Distinct Morphologies Respond Selectively to Physiological and Pathological Stimuli and Aging

inferredcites →https://doi.org/10.1016/j.stem.2016.06.013openalex-snapshot

Age-Dependent Niche Signals from the Choroid Plexus Regulate Adult Neural Stem Cells

inferredcites →https://doi.org/10.1016/j.stem.2018.03.015openalex-snapshot

Human Hippocampal Neurogenesis Persists throughout Aging

inferredcites →https://doi.org/10.1016/j.stem.2018.04.004openalex-snapshot

Human Adult Neurogenesis: Evidence and Remaining Questions

inferredcites →https://doi.org/10.1016/j.stem.2018.11.006openalex-snapshot

Does Adult Neurogenesis Persist in the Human Hippocampus?

inferredcites →https://doi.org/10.1016/j.stemcr.2017.06.014openalex-snapshot

Hippocampal TERT Regulates Spatial Memory Formation through Modulation of Neural Development

inferredcites →https://doi.org/10.1016/s0092-8674(00)80783-7openalex-snapshot

Subventricular Zone Astrocytes Are Neural Stem Cells in the Adult Mammalian Brain

inferredcites →https://doi.org/10.1016/s1044-7431(03)00103-9openalex-snapshot

Telomerase activity in the subventricular zone of adult mice

inferredcites →https://doi.org/10.1021/acschemneuro.9b00063openalex-snapshot

The Curious Case of Human Hippocampal Neurogenesis

inferredcites →https://doi.org/10.1023/a:1014016315003openalex-snapshot

Neural stem cells lose telomerase activity upon differentiating into astrocytes

inferredcites →https://doi.org/10.1023/a:1025783412651openalex-snapshot

Identity, distribution, and development of polydendrocytes: NG2-expressing glial cells

inferredcites →https://doi.org/10.1038/3305openalex-snapshot

Neurogenesis in the adult human hippocampus

inferredcites →https://doi.org/10.1038/nature09603openalex-snapshot

Telomerase reactivation reverses tissue degeneration in aged telomerase-deficient mice

inferredcites →https://doi.org/10.1038/nature25975openalex-snapshot

Human hippocampal neurogenesis drops sharply in children to undetectable levels in adults

inferredcites →https://doi.org/10.1038/nmeth758openalex-snapshot

Neural stem cells and neurospheres—re-evaluating the relationship

inferredcites →https://doi.org/10.1038/nrm3591openalex-snapshot

Molecular regulation of stem cell quiescence

inferredcites →https://doi.org/10.1038/nrn3921openalex-snapshot

Development and functions of the choroid plexus–cerebrospinal fluid system

inferredcites →https://doi.org/10.1038/s41586-018-0004-7openalex-snapshot

Distributed hepatocytes expressing telomerase repopulate the liver in homeostasis and injury

inferredcites →https://doi.org/10.1038/s41596-019-0267-yopenalex-snapshot

Unraveling human adult hippocampal neurogenesis

inferredcites →https://doi.org/10.1038/s41598-017-06150-xopenalex-snapshot

Neurogenesis from Sox2 expressing cells in the adult cerebellar cortex

inferredcites →https://doi.org/10.1038/sj.onc.1201933openalex-snapshot

Expression of mouse telomerase reverse transcriptase during development, differentiation and proliferation

inferredcites →https://doi.org/10.1073/pnas.0508964102openalex-snapshot

Differential cis-regulation of human versus mouse TERT gene expression in vivo : Identification of a human-specific repressive element

inferredcites →https://doi.org/10.1073/pnas.0804800105openalex-snapshot

Generation of mTert -GFP mice as a model to identify and study tissue progenitor cells

inferredcites →https://doi.org/10.1073/pnas.1013004108openalex-snapshot

Mouse telomerase reverse transcriptase (mTert) expression marks slowly cycling intestinal stem cells

inferredcites →https://doi.org/10.1073/pnas.89.18.8591openalex-snapshot

De novo generation of neuronal cells from the adult mouse brain.

inferredcites →https://doi.org/10.1073/pnas.95.18.10471openalex-snapshot

Expression of mouse telomerase catalytic subunit in embryos and adult tissues

inferredcites →https://doi.org/10.1074/jbc.m007378200openalex-snapshot

NF-κB Regulates Transcription of the Mouse Telomerase Catalytic Subunit

inferredcites →https://doi.org/10.1089/scd.2011.0279openalex-snapshot

Ischemia-Induced Neural Stem/Progenitor Cells in the Pia Mater Following Cortical Infarction

inferredcites →https://doi.org/10.1089/scd.2018.0133openalex-snapshot

Telomerase Reverse Transcriptase Expression in Mouse Endometrium During Reepithelialization and Regeneration in a Menses-Like Model

inferredcites →https://doi.org/10.1093/cercor/bhy096openalex-snapshot

Hippocampal Radial Glial Subtypes and Their Neurogenic Potential in Human Fetuses and Healthy and Alzheimer’s Disease Adults

inferredcites →https://doi.org/10.1093/molehr/3.9.769openalex-snapshot

Developmental regulation of telomerase activity in human fetal tissues during gestation

inferredcites →https://doi.org/10.1093/molehr/gav076openalex-snapshot

The mouse endometrium contains epithelial, endothelial and leucocyte populations expressing the stem cell marker telomerase reverse transcriptase

inferredcites →https://doi.org/10.1093/stmcls/sxab005openalex-snapshot

Telomerase Reverse Transcriptase Expression Marks a Population of Rare Adipose Tissue Stem Cells

inferredcites →https://doi.org/10.1096/fasebj.13.15.2091openalex-snapshot

Studies of the molecular mechanisms in the regulation of telomerase activity

inferredcites →https://doi.org/10.1096/fj.12-208843openalex-snapshot

Telomerase expression in the mammalian heart

inferredcites →https://doi.org/10.1101/cshperspect.a018820openalex-snapshot

The Adult Ventricular–Subventricular Zone (V-SVZ) and Olfactory Bulb (OB) Neurogenesis

inferredcites →https://doi.org/10.1101/cshperspect.a018945openalex-snapshot

Adult Olfactory Bulb Neurogenesis

inferredcites →https://doi.org/10.1111/ahe.12496openalex-snapshot

Adult neurogenesis in the mammalian dentate gyrus

inferredcites →https://doi.org/10.1111/nan.12337openalex-snapshot

Human adult neurogenesis across the ages: An immunohistochemical study

inferredcites →https://doi.org/10.1126/science.1115360openalex-snapshot

Neurogenesis in the Hypothalamus of Adult Mice: Potential Role in Energy Balance

inferredcites →https://doi.org/10.1126/science.1553558openalex-snapshot

Generation of Neurons and Astrocytes from Isolated Cells of the Adult Mammalian Central Nervous System

inferredcites →https://doi.org/10.1126/science.6474166openalex-snapshot

Neurons Generated in the Adult Brain Are Recruited into Functional Circuits

inferredcites →https://doi.org/10.1134/s0006297910130055openalex-snapshot

Telomerase: Structure, functions, and activity regulation

inferredcites →https://doi.org/10.1155/2015/727542openalex-snapshot

Molecular Biomarkers for Embryonic and Adult Neural Stem Cell and Neurogenesis

inferredcites →https://doi.org/10.1177/1073858420954826openalex-snapshot

Meninges: A Widespread Niche of Neural Progenitors for the Brain

inferredcites →https://doi.org/10.1177/2516865718820946openalex-snapshot

Impact of Metabolic Pathways and Epigenetics on Neural Stem Cells

inferredcites →https://doi.org/10.1371/journal.pone.0008809openalex-snapshot

Murine Features of Neurogenesis in the Human Hippocampus across the Lifespan from 0 to 100 Years

inferredcites →https://doi.org/10.1523/jneurosci.06-01-00208.1986openalex-snapshot

Neurons of the olfactory epithelium in adult rats contain vimentin

inferredcites →https://doi.org/10.1523/jneurosci.0675-20.2020openalex-snapshot

Evidences for Adult Hippocampal Neurogenesis in Humans

inferredcites →https://doi.org/10.1523/jneurosci.0676-20.2020openalex-snapshot

Positive Controls in Adults and Children Support That Very Few, If Any, New Neurons Are Born in the Adult Human Hippocampus

inferredcites →https://doi.org/10.1523/jneurosci.0805-11.2011openalex-snapshot

Hippocampal Telomerase Is Involved in the Modulation of Depressive Behaviors

inferredcites →https://doi.org/10.1523/jneurosci.22-14-06106.2002openalex-snapshot

Maturation and Death of Adult-Born Olfactory Bulb Granule Neurons: Role of Olfaction

inferredcites →https://doi.org/10.1523/jneurosci.2925-14.2015openalex-snapshot

The Role of Telomerase Protein TERT in Alzheimer's Disease and in Tau-Related Pathology In Vitro

inferredcites →https://doi.org/10.1523/jneurosci.3836-09.2009openalex-snapshot

Telomere Shortening in Neural Stem Cells Disrupts Neuronal Differentiation and Neuritogenesis

inferredcites →https://doi.org/10.1681/asn.2011050447openalex-snapshot

Characterization and Fate of Telomerase-expressing Epithelia during Kidney Repair

inferredcites →https://doi.org/10.3389/fcell.2019.00274openalex-snapshot

Mitochondria, Telomeres and Telomerase Subunits

inferredcites →https://doi.org/10.3389/fgene.2018.00345openalex-snapshot

The Telomerase Complex Directly Controls Hematopoietic Stem Cell Differentiation and Senescence in an Induced Pluripotent Stem Cell Model of Telomeropathy

inferredcites →https://doi.org/10.3389/fncel.2020.00198openalex-snapshot

Overview of General and Discriminating Markers of Differential Microglia Phenotypes

inferredcites →https://doi.org/10.3389/fncel.2020.576444openalex-snapshot

Beyond the Hippocampus and the SVZ: Adult Neurogenesis Throughout the Brain

inferredcites →https://doi.org/10.3389/fnins.2014.00157openalex-snapshot

Dietary and sex-specific factors regulate hypothalamic neurogenesis in young adult mice

inferredcites →https://doi.org/10.3389/fnins.2015.00387openalex-snapshot

Hypothalamic tanycytes—masters and servants of metabolic, neuroendocrine, and neurogenic functions

inferredcites →https://doi.org/10.3389/fnins.2018.00706openalex-snapshot

Comparing Adult Hippocampal Neurogenesis Across Species: Translating Time to Predict the Tempo in Humans

inferredcites →https://doi.org/10.3389/fnins.2019.00923openalex-snapshot

Perspective: Of Mice and Men – How Widespread Is Adult Neurogenesis?

inferredcites →https://doi.org/10.3389/fnins.2020.00839openalex-snapshot

Understanding the Real State of Human Adult Hippocampal Neurogenesis From Studies of Rodents and Non-human Primates

inferredcites →https://doi.org/10.3389/fnmol.2018.00160openalex-snapshot

The Emerging Roles for Telomerase in the Central Nervous System

inferredcites →https://doi.org/10.3390/genes7060027openalex-snapshot

Telomerase Activity is Downregulated Early During Human Brain Development

inferredcites →https://doi.org/10.3978/j.issn.2305-5839.2014.09.05openalex-snapshot

Chemically defined serum-free and xeno-free media for multiple cell lineages.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1007/s12975-022-01109-1openalex-snapshot

Stroke and Neurogenesis: Bridging Clinical Observations to New Mechanistic Insights from Animal Models

inferred← citeshttps://doi.org/10.1096/fba.2025-00300openalex-snapshot

Methodological Challenges for Ablation of BMPR1A in Hypothalamic Tanycytes—A Cautionary Tale

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