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Activating Transcription Factor 3 (ATF3) is a Highly Conserved Pro-regenerative Transcription Factor in the Vertebrate Nervous System

https://doi.org/10.3389/fcell.2022.824036

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What this work says

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

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Regenerated synapses in lamprey spinal cord are sparse and small even after functional recovery from injury

inferredcites →https://doi.org/10.1002/cne.901680407openalex-snapshot

Regeneration of Müller and Mauthner axons after spinal transection in larval lampreys

inferredcites →https://doi.org/10.1002/dneu.20934openalex-snapshot

Multiple transcription factor families regulate axon growth and regeneration

inferredcites →https://doi.org/10.1002/dneu.22637openalex-snapshot

Intrinsic Determinants of Axon Regeneration

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Genetic Approaches to Neurotrauma Research: Opportunities and Potential Pitfalls of Murine Models

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Activating Transcription Factor 3 (ATF3) Induction by Axotomy in Sensory and Motoneurons: A Novel Neuronal Marker of Nerve Injury

inferredcites →https://doi.org/10.1007/s12017-014-8329-3openalex-snapshot

Spinal Cord Injury and the Neuron-Intrinsic Regeneration-Associated Gene Program

inferredcites →https://doi.org/10.1016/j.bbrc.2017.05.079openalex-snapshot

Activating transcription factor 3 promotes spinal cord regeneration of adult zebrafish

inferredcites →https://doi.org/10.1016/j.conb.2016.04.005openalex-snapshot

The multicellular complexity of peripheral nerve regeneration

inferredcites →https://doi.org/10.1016/j.expneurol.2013.12.023openalex-snapshot

Non-mammalian model systems for studying neuro-immune interactions after spinal cord injury

inferredcites →https://doi.org/10.1016/j.expneurol.2016.02.022openalex-snapshot

Learning to swim, again: Axon regeneration in fish

inferredcites →https://doi.org/10.1016/j.expneurol.2016.03.004openalex-snapshot

Hyperactivated Stat3 boosts axon regeneration in the CNS

inferredcites →https://doi.org/10.1016/j.expneurol.2016.06.002openalex-snapshot

Cutaneous tissue damage induces long-lasting nociceptive sensitization and regulation of cellular stress- and nerve injury-associated genes in sensory neurons

inferredcites →https://doi.org/10.1016/j.jns.2011.08.037openalex-snapshot

Enhancing intrinsic growth capacity promotes adult CNS regeneration

inferredcites →https://doi.org/10.1016/j.livres.2017.08.001openalex-snapshot

Activating transcription factor 3 in immune response and metabolic regulation

inferredcites →https://doi.org/10.1016/j.mcn.2006.03.005openalex-snapshot

The transcription factor ATF-3 promotes neurite outgrowth

inferredcites →https://doi.org/10.1016/j.mcn.2018.08.001openalex-snapshot

The effect of Jun dimerization on neurite outgrowth and motif binding

inferredcites →https://doi.org/10.1016/j.neulet.2016.12.033openalex-snapshot

The role of cAMP and its downstream targets in neurite growth in the adult nervous system

inferredcites →https://doi.org/10.1016/j.neuron.2016.01.034openalex-snapshot

A Systems-Level Analysis of the Peripheral Nerve Intrinsic Axonal Growth Program

inferredcites →https://doi.org/10.1016/j.tins.2018.02.012openalex-snapshot

The Paper that Restarted Modern Central Nervous System Axon Regeneration Research

inferredcites →https://doi.org/10.1038/nature11499openalex-snapshot

Skin shedding and tissue regeneration in African spiny mice (Acomys)

inferredcites →https://doi.org/10.1038/ng.2568openalex-snapshot

Sequencing of the sea lamprey (Petromyzon marinus) genome provides insights into vertebrate evolution

inferredcites →https://doi.org/10.1038/nrn2707openalex-snapshot

Considering the evolution of regeneration in the central nervous system

inferredcites →https://doi.org/10.1038/nrneurol.2013.227openalex-snapshot

Advances in peripheral nerve regeneration

inferredcites →https://doi.org/10.1038/s41598-017-18757-1openalex-snapshot

Highly conserved molecular pathways, including Wnt signaling, promote functional recovery from spinal cord injury in lampreys

inferredcites →https://doi.org/10.1038/s41598-019-50485-6openalex-snapshot

Cellular reprogramming for successful CNS axon regeneration is driven by a temporally changing cast of transcription factors

inferredcites →https://doi.org/10.1038/s41598-020-79624-0openalex-snapshot

Ascending dorsal column sensory neurons respond to spinal cord injury and downregulate genes related to lipid metabolism

inferredcites →https://doi.org/10.1042/bj20121807openalex-snapshot

Spinal cord regeneration: where fish, frogs and salamanders lead the way, can we follow?

inferredcites →https://doi.org/10.1046/j.1460-9568.2003.02809.xopenalex-snapshot

Corticospinal neurons up‐regulate a range of growth‐associated genes following intracortical, but not spinal, axotomy

inferredcites →https://doi.org/10.1073/pnas.1120684109openalex-snapshot

Krüppel-like Factor 7 engineered for transcriptional activation promotes axon regeneration in the adult corticospinal tract

inferredcites →https://doi.org/10.1073/pnas.83.8.2763openalex-snapshot

Functional regeneration following spinal transection demonstrated in the isolated spinal cord of the larval sea lamprey.

inferredcites →https://doi.org/10.1073/pnas.88.9.3720openalex-snapshot

Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity.

inferredcites →https://doi.org/10.1074/jbc.271.3.1695openalex-snapshot

ATF3 Gene

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Neuroinflammation after Traumatic Brain Injury Is Enhanced in Activating Transcription Factor 3 Mutant Mice

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Overexpression of ATF3 or the combination of ATF3, c-Jun, STAT3 and Smad1 promotes regeneration of the central axon branch of sensory neurons but without synergistic effects

inferredcites →https://doi.org/10.1098/rsob.160091openalex-snapshot

Atf3 mutant mice show reduced axon regeneration and impaired regeneration-associated gene induction after peripheral nerve injury

inferredcites →https://doi.org/10.1101/2021.04.28.441862openalex-snapshot

A Single Cell Atlas of Spared Tissue Below a Spinal Cord Injury Reveals Cellular Mechanisms of Repair

inferredcites →https://doi.org/10.1111/j.1460-9568.2005.04530.xopenalex-snapshot

Spinal cord compression and dorsal root injury cause up‐regulation of activating transcription factor‐3 in large‐diameter dorsal root ganglion neurons

inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05597.xopenalex-snapshot

Identification of candidate transcriptional modulators involved in successful regeneration after nerve injury

inferredcites →https://doi.org/10.1113/jphysiol.1978.sp012280openalex-snapshot

Mechanisms of functional recovery and regeneration after spinal cord transection in larval sea lamprey.

inferredcites →https://doi.org/10.1126/science.6171034openalex-snapshot

Axonal Elongation into Peripheral Nervous System "Bridges" After Central Nervous System Injury in Adult Rats

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Interactions among LRF-1, JunB, c-Jun, and c-Fos define a regulatory program in the G1 phase of liver regeneration.

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Interactions among LRF-1, JunB, c-Jun, and c-Fos Define a Regulatory Program in the G 1 Phase of Liver Regeneration

inferredcites →https://doi.org/10.1146/annurev-vision-022720-094953openalex-snapshot

Axon Regeneration in the Mammalian Optic Nerve

inferredcites →https://doi.org/10.1167/iovs.61.2.31openalex-snapshot

Activating Transcription Factor 3 (ATF3) Protects Retinal Ganglion Cells and Promotes Functional Preservation After Optic Nerve Crush

inferredcites →https://doi.org/10.1186/1471-2164-14-583openalex-snapshot

Genome-wide gene expression profiling of stress response in a spinal cord clip compression injury model

inferredcites →https://doi.org/10.1186/s12862-016-0598-zopenalex-snapshot

The diversification of the basic leucine zipper family in eukaryotes correlates with the evolution of multicellularity

inferredcites →https://doi.org/10.1201/9781315120188-26openalex-snapshot

Spinal cord repair and regeneration

inferredcites →https://doi.org/10.1242/dev.167718openalex-snapshot

Model systems for regeneration: the spiny mouse, Acomys cahirinus

inferredcites →https://doi.org/10.1242/dmm.044131openalex-snapshot

Building bridges, not walls: spinal cord regeneration in zebrafish

inferredcites →https://doi.org/10.1371/journal.pone.0084212openalex-snapshot

Genome Wide Expression Profiling during Spinal Cord Regeneration Identifies Comprehensive Cellular Responses in Zebrafish

inferredcites →https://doi.org/10.1523/jneurosci.0846-13.2013openalex-snapshot

TrkB.T1 Contributes to Neuropathic Pain after Spinal Cord Injury through Regulation of Cell Cycle Pathways

inferredcites →https://doi.org/10.1523/jneurosci.5103-10.2011openalex-snapshot

Diffuse Traumatic Axonal Injury in the Mouse Induces Atrophy, c-Jun Activation, and Axonal Outgrowth in the Axotomized Neuronal Population

inferredcites →https://doi.org/10.1523/jneurosci.5313-06.2007openalex-snapshot

ATF3 Increases the Intrinsic Growth State of DRG Neurons to Enhance Peripheral Nerve Regeneration

inferredcites →https://doi.org/10.2741/3993openalex-snapshot

Deer antler innervation and regeneration

inferredcites →https://doi.org/10.3233/rnn-2008-00443openalex-snapshot

Adult zebrafish as a model for successful central nervous system regeneration

inferredcites →https://doi.org/10.3389/fendo.2020.00556openalex-snapshot

Master Regulator Activating Transcription Factor 3 (ATF3) in Metabolic Homeostasis and Cancer

inferredcites →https://doi.org/10.3389/fnmol.2015.00026openalex-snapshot

Looking downstream: the role of cyclic AMP-regulated genes in axonal regeneration

inferredcites →https://doi.org/10.3389/fnmol.2015.00043openalex-snapshot

What makes a RAG regeneration associated?

inferredcites →https://doi.org/10.3389/fphar.2016.00119openalex-snapshot

E2F4 Promotes Neuronal Regeneration and Functional Recovery after Spinal Cord Injury in Zebrafish

inferredcites →https://doi.org/10.3390/ijms21228652openalex-snapshot

Peripheral Nerve Regeneration and Muscle Reinnervation

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ATF3, a Hub of the Cellular Adaptive-Response Network, in the Pathogenesis of Diseases: Is Modulation of Inflammation a Unifying Component?

inferredcites →https://doi.org/10.7554/elife.19272openalex-snapshot

Combinatorial bZIP dimers display complex DNA-binding specificity landscapes

What points at this work

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

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Ezrin, a novel marker of ependymal cells, can be used to demonstrate their proliferation regulation after spinal cord injury in mice

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ATF3-dependent formation of inclusion bodies in polyQ-expressing human iPSC-derived neurons confers cellular protection

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Spinal cord regeneration deploys cell-type specific developmental and non-developmental strategies to restore neuron diversity

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Cancer-induced nerve injury promotes resistance to anti-PD-1 therapy

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ATF3 overexpression is associated with cardiac hypertrophy and electrical dysfunction accompanied by enhanced cardiac cell proliferation in zebrafish

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Additional file 1 of MSC-derived mitochondria promote axonal regeneration via Atf3 gene up-regulation by ROS induced DNA double strand breaks at transcription initiation region

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Additional file 2 of MSC-derived mitochondria promote axonal regeneration via Atf3 gene up-regulation by ROS induced DNA double strand breaks at transcription initiation region

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