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Aerobic glycolysis is important for zebrafish larval wound closure and tail regeneration

https://doi.org/10.1111/wrr.13050
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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/aja.1002030302openalex-snapshot
Stages of embryonic development of the zebrafish
inferredcites →https://doi.org/10.1002/bies.201300110openalex-snapshot
Carbohydrate metabolism during vertebrate appendage regeneration: What is its role? How is it regulated?
inferredcites →https://doi.org/10.1002/dvdy.10220openalex-snapshot
Tales of regeneration in zebrafish
inferredcites →https://doi.org/10.1002/dvdy.20181openalex-snapshot
Early fin primordia of zebrafish larvae regenerate by a similar growth control mechanism with adult regeneration
inferredcites →https://doi.org/10.1002/dvdy.23977openalex-snapshot
Characterization of TGFβ signaling during tail regeneration in the leopard Gecko (Eublepharis macularius)
inferredcites →https://doi.org/10.1002/stem.1552openalex-snapshot
HIF1α Modulates Cell Fate Reprogramming Through Early Glycolytic Shift and Upregulation of PDK1–3 and PKM2
inferredcites →https://doi.org/10.1007/s00018-012-0928-2openalex-snapshot
Cytoskeleton responses in wound repair
inferredcites →https://doi.org/10.1007/s40139-018-0161-2openalex-snapshot
Tissue Repair and Epimorphic Regeneration: an Overview
inferredcites →https://doi.org/10.1016/j.bmcl.2013.04.001openalex-snapshot
Identification of substituted 2-thio-6-oxo-1,6-dihydropyrimidines as inhibitors of human lactate dehydrogenase
inferredcites →https://doi.org/10.1016/j.ccell.2016.02.018openalex-snapshot
mTORC1-Dependent Metabolic Reprogramming Underlies Escape from Glycolysis Addiction in Cancer Cells
inferredcites →https://doi.org/10.1016/j.ceca.2020.102329openalex-snapshot
Lactate as a new second messenger shaping intracellular Mg2+ dynamics and bioenergetics
inferredcites →https://doi.org/10.1016/j.cell.2016.05.035openalex-snapshot
Mitochondrial Dynamics Controls T Cell Fate through Metabolic Programming
inferredcites →https://doi.org/10.1016/j.cell.2016.11.037openalex-snapshot
Emerging Biological Principles of Metastasis
inferredcites →https://doi.org/10.1016/j.cmet.2011.06.011openalex-snapshot
Somatic Oxidative Bioenergetics Transitions into Pluripotency-Dependent Glycolysis to Facilitate Nuclear Reprogramming
inferredcites →https://doi.org/10.1016/j.cmet.2015.10.010openalex-snapshot
In Vivo Evidence for a Lactate Gradient from Astrocytes to Neurons
inferredcites →https://doi.org/10.1016/j.cmet.2017.06.021openalex-snapshot
Neuronal Stimulation Triggers Neuronal Glycolysis and Not Lactate Uptake
inferredcites →https://doi.org/10.1016/j.devcel.2017.08.024openalex-snapshot
Tension Creates an Endoreplication Wavefront that Leads Regeneration of Epicardial Tissue
inferredcites →https://doi.org/10.1016/j.exphem.2019.02.004openalex-snapshot
ATP produced by anaerobic glycolysis is essential for enucleation of human erythroblasts
inferredcites →https://doi.org/10.1016/s0021-9258(18)64988-9openalex-snapshot
LOCALIZATION OF THE PRIMARY METABOLIC BLOCK PRODUCED BY 2-DEOXYGLUCOSE
inferredcites →https://doi.org/10.1017/s0016672303216384openalex-snapshot
Zebrafish: A Practical Approach. Edited by C. NÜSSLEIN-VOLHARD and R. DAHM. Oxford University Press. 2002. 322 pages. ISBN 0 19 963808 X. Price £40.00 (paperback). ISBN 0 19 963809 8. Price £80.00 (hardback).
inferredcites →https://doi.org/10.1021/jf940698yopenalex-snapshot
Mechanism for Stabilization of Fish Actomyosin by Sodium Lactate
inferredcites →https://doi.org/10.1038/35073086openalex-snapshot
The myosin swinging cross-bridge model
inferredcites →https://doi.org/10.1038/emboj.2012.71openalex-snapshot
HIF1α induced switch from bivalent to exclusively glycolytic metabolism during ESC‐to‐EpiSC/hESC transition
inferredcites →https://doi.org/10.1038/ncomms3550openalex-snapshot
Imaging energy status in live cells with a fluorescent biosensor of the intracellular ATP-to-ADP ratio
inferredcites →https://doi.org/10.1038/nmeth.4306openalex-snapshot
Genetically encoded fluorescent sensors reveal dynamic regulation of NADPH metabolism
inferredcites →https://doi.org/10.1038/s41467-018-06460-2openalex-snapshot
Damage-induced reactive oxygen species enable zebrafish tail regeneration by repositioning of Hedgehog expressing cells
inferredcites →https://doi.org/10.1038/s41467-018-06614-2openalex-snapshot
Early redox activities modulate Xenopus tail regeneration
inferredcites →https://doi.org/10.1038/s41536-021-00163-xopenalex-snapshot
The Warburg effect is necessary to promote glycosylation in the blastema during zebrafish tail regeneration
inferredcites →https://doi.org/10.1038/s41598-018-38455-wopenalex-snapshot
Cdh2 coordinates Myosin-II dependent internalisation of the zebrafish neural plate
inferredcites →https://doi.org/10.1046/j.1471-4159.1996.66062606.xopenalex-snapshot
Chronic In Vivo Sodium Azide Infusion Induces Selective and Stable Inhibition of Cytochrome c Oxidase
inferredcites →https://doi.org/10.1089/ars.2006.1467openalex-snapshot
A High Glycolytic Flux Supports the Proliferative Potential of Murine Embryonic Stem Cells
inferredcites →https://doi.org/10.1101/gr.143000openalex-snapshot
DNA Cloning Using In Vitro Site-Specific Recombination
inferredcites →https://doi.org/10.1111/j.1365-2621.1994.tb06907.xopenalex-snapshot
Actomyosin Stabilization to Freeze‐Thaw and Heat Denaturation by Lactate Salts
inferredcites →https://doi.org/10.1111/wrr.13050openalex-snapshot
Aerobic glycolysis is important for zebrafish larval wound closure and tail regeneration
inferredcites →https://doi.org/10.1126/science.1077857openalex-snapshot
Heart Regeneration in Zebrafish
inferredcites →https://doi.org/10.1126/science.aac4357openalex-snapshot
Mitochondrial dysfunction and longevity in animals: Untangling the knot
inferredcites →https://doi.org/10.1146/annurev-cellbio-092910-154237openalex-snapshot
Aerobic Glycolysis: Meeting the Metabolic Requirements of Cell Proliferation
inferredcites →https://doi.org/10.1152/physrev.00031.2010openalex-snapshot
Fiber Types in Mammalian Skeletal Muscles
inferredcites →https://doi.org/10.1155/2017/6797460openalex-snapshot
The Involvement of Mg2+ in Regulation of Cellular and Mitochondrial Functions
inferredcites →https://doi.org/10.1155/2017/9029327openalex-snapshot
HIF1 α -Induced Glycolysis Metabolism Is Essential to the Activation of Inflammatory Macrophages
inferredcites →https://doi.org/10.1158/jcr.1925.148openalex-snapshot
The Metabolism of Carcinoma Cells
inferredcites →https://doi.org/10.1172/jci39104openalex-snapshot
The basics of epithelial-mesenchymal transition
inferredcites →https://doi.org/10.1186/1476-4598-8-32openalex-snapshot
The role of cellular oxidative stress in regulating glycolysis energy metabolism in hepatoma cells
inferredcites →https://doi.org/10.1186/1476-4598-9-33openalex-snapshot
Warburg effect in chemosensitivity: Targeting lactate dehydrogenase-A re-sensitizes Taxol-resistant cancer cells to Taxol
inferredcites →https://doi.org/10.1242/dev.059345openalex-snapshot
Ubiquitous transgene expression and Cre-based recombination driven by the ubiquitin promoter in zebrafish
inferredcites →https://doi.org/10.1242/dev.066498openalex-snapshot
pTransgenesis: a cross-species, modular transgenesis resource
inferredcites →https://doi.org/10.1242/dev.128389openalex-snapshot
Metabolic remodeling during the loss and acquisition of pluripotency
inferredcites →https://doi.org/10.1371/journal.pone.0051766openalex-snapshot
In Vivo Cell and Tissue Dynamics Underlying Zebrafish Fin Fold Regeneration
inferredcites →https://doi.org/10.1371/journal.pone.0057712openalex-snapshot
A Genetically Encoded FRET Lactate Sensor and Its Use To Detect the Warburg Effect in Single Cancer Cells
inferredcites →https://doi.org/10.1387/ijdb.103198apopenalex-snapshot
Modulation of mitochondrial biogenesis and bioenergetic metabolism upon in vitro and in vivo differentiation of human ES and iPS cells
inferredcites →https://doi.org/10.3389/fmicb.2015.00742openalex-snapshot
NADPH-generating systems in bacteria and archaea
inferredcites →https://doi.org/10.3390/ijms20020238openalex-snapshot
HIF-1-Dependent Reprogramming of Glucose Metabolic Pathway of Cancer Cells and Its Therapeutic Significance
inferredcites →https://doi.org/10.3390/ijms21010234openalex-snapshot
2-Deoxy-d-Glucose and Its Analogs: From Diagnostic to Therapeutic Agents
inferredcites →https://doi.org/10.7554/elife.13374openalex-snapshot
Metabolic reprogramming during neuronal differentiation from aerobic glycolysis to neuronal oxidative phosphorylation
inferredcites →https://doi.org/10.7554/elife.50163openalex-snapshot
Single-cell analysis uncovers that metabolic reprogramming by ErbB2 signaling is essential for cardiomyocyte proliferation in the regenerating heart
inferredcites →https://doi.org/10.7554/elife.76987openalex-snapshot
A regeneration-triggered metabolic adaptation is necessary for cell identity transitions and cell cycle re-entry to support blastema formation and bone regeneration

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4753794openalex-extracted
HDAC Activity Inhibition Alters Histone H4 Acetylation Dynamics Coupled to HDAC Expression and Lipid Mediator 12(S)HETE Biogenesis in Xenopus laevis Tail Regeneration
inferred← citeshttps://doi.org/10.1002/jbt.23752openalex-snapshot
HOXC6‐mediated transcriptional activation of ENO2 promotes oral squamous cell carcinoma progression through the Warburg effect
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111552openalex-snapshot
Elevated pentose phosphate pathway flux supports appendage regeneration
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106147openalex-snapshot
Duox is the primary NADPH oxidase responsible for ROS production during adult caudal fin regeneration in zebrafish
inferred← citeshttps://doi.org/10.1016/j.jbc.2025.110298openalex-snapshot
Hypoxia-inducible factor-1 alpha modulates muscle growth and the molting process through its regulation of glycolysis in Neocaridina davidi
inferred← citeshttps://doi.org/10.1016/j.jbc.2026.113605openalex-snapshot
Spiny mouse fibroblasts exhibit a baseline preference for glycolysis and are resilient to oxidative stress across lifespan
inferred← citeshttps://doi.org/10.1016/j.jid.2024.04.003openalex-snapshot
Dermal Dive: An Overview of Cutaneous Wounding Techniques in Zebrafish
inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106211openalex-snapshot
Enlightening brain energy metabolism
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.07.004openalex-snapshot
Intracellular pH dynamics promotes zebrafish larval tail regeneration
inferred← citeshttps://doi.org/10.1038/s41536-021-00163-xopenalex-snapshot
The Warburg effect is necessary to promote glycosylation in the blastema during zebrafish tail regeneration
inferred← citeshttps://doi.org/10.1038/s41580-024-00733-zopenalex-snapshot
Epithelial–mesenchymal transition in tissue repair and degeneration
inferred← citeshttps://doi.org/10.1101/2025.04.21.649771openalex-snapshot
Early epigenetic priming of regeneration studied with a novel transgenic epigenetic reporter
inferred← citeshttps://doi.org/10.1101/2025.10.02.680123openalex-snapshot
Active mitochondria in healthy spiny mouse fibroblasts resemble megamitochondria and remain resilient across lifespan
inferred← citeshttps://doi.org/10.1111/wrr.13234openalex-snapshot
A novel method to assess photobiomodulation in stimulating regenerative capacity and vascularization in zebrafish
inferred← citeshttps://doi.org/10.1186/s43556-026-00558-6openalex-snapshot
Lactate metabolism and protein lactylation in inflammatory and tumor microenvironments
inferred← citeshttps://doi.org/10.1242/dev.202360openalex-snapshot
Pathway to Independence: the future of developmental biology
inferred← citeshttps://doi.org/10.1242/dev.202541openalex-snapshot
Mechanisms of regeneration: to what extent do they recapitulate development?
inferred← citeshttps://doi.org/10.1242/dmm.049801openalex-snapshot
Parallel repair mechanisms in plants and animals
inferred← citeshttps://doi.org/10.1242/jeb.249704openalex-snapshot
Mitochondrial respiration capacity impacts gill tissue regeneration in Atlantic salmon
inferred← citeshttps://doi.org/10.1242/jeb.250750openalex-snapshot
Regeneration physiology of invertebrates
inferred← citeshttps://doi.org/10.12794/metadc2179343openalex-snapshot
Hypoxia-Induced Cardiac Arrest Alters Central Nervous System Concentrations of the GLYT2 Glycine Transporter in Zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.3389/fcell.2025.1529093openalex-snapshot
Xenopus laevis neural stem progenitor cells exhibit a transient metabolic shift toward glycolysis during spinal cord regeneration
inferred← citeshttps://doi.org/10.3389/fimmu.2022.806484openalex-snapshot
Gill and Liver Transcript Expression Changes Associated With Gill Damage in Atlantic Salmon (Salmo salar)
inferred← citeshttps://doi.org/10.3389/fphys.2021.771040openalex-snapshot
Tissues and Cell Types of Appendage Regeneration: A Detailed Look at the Wound Epidermis and Its Specialized Forms
inferred← citeshttps://doi.org/10.3390/ijms24098314openalex-snapshot
Modeling Human Muscular Dystrophies in Zebrafish: Mutant Lines, Transgenic Fluorescent Biosensors, and Phenotyping Assays
inferred← citeshttps://doi.org/10.3390/metabo15070449openalex-snapshot
Metabolic Changes in Zebrafish Larvae Infected with Mycobacterium marinum: A Widely Targeted Metabolomic Analysis
inferred← citeshttps://doi.org/10.3892/mmr.2022.12886openalex-snapshot
Dedifferentiation and in vivo reprogramming of committed cells in wound repair (Review)
inferred← citeshttps://doi.org/10.46889/jrmbr.2026.7207openalex-snapshot
Hypothesis and Reflections on the Bases of Regeneration-Incompetence: Healing Through a Fibrotic Scarring Process
inferred← citeshttps://doi.org/10.70675/60a97388z3f39z4829zbe4ezd73224b4a333openalex-snapshot
Exploiting Leishmania/macrophage interaction for the discovery of novel, host-directed drug targets : identification of the RNA-binding protein IGF2BP2 as a crucial factor in immune-metabolic reprogramming of Leishmania-infected macrophages (LIMs)
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