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Two Independent Functions of Collier/Early B Cell Factor in the Control of Drosophila Blood Cell Homeostasis

https://doi.org/10.1371/journal.pone.0148978
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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/dvg.20711openalex-snapshot
Odd‐skipped maintains prohemocyte potency and blocks blood cell development in Drosophila
inferredcites →https://doi.org/10.1006/dbio.2000.0123openalex-snapshot
Postembryonic Hematopoiesis in Drosophila
inferredcites →https://doi.org/10.1006/dbio.2001.0542openalex-snapshot
Cellular Immune Response to Parasite Infection in the Drosophila Lymph Gland Is Developmentally Regulated
inferredcites →https://doi.org/10.1007/s00427-011-0364-6openalex-snapshot
Hematopoiesis at the onset of metamorphosis: terminal differentiation and dissociation of the Drosophila lymph gland
inferredcites →https://doi.org/10.1016/j.bbagen.2012.06.005openalex-snapshot
Signal transduction pathways, intrinsic regulators, and the control of cell fate choice
inferredcites →https://doi.org/10.1016/j.bbrc.2014.09.109openalex-snapshot
bantam miRNA is important for Drosophila blood cell homeostasis and a regulator of proliferation in the hematopoietic progenitor niche
inferredcites →https://doi.org/10.1016/j.cell.2011.11.041openalex-snapshot
Interaction between Differentiating Cell- and Niche-Derived Signals in Hematopoietic Progenitor Maintenance
inferredcites →https://doi.org/10.1016/j.cell.2013.10.032openalex-snapshot
Olfactory Control of Blood Progenitor Maintenance
inferredcites →https://doi.org/10.1016/j.cub.2014.09.081openalex-snapshot
Yorkie and Scalloped Signaling Regulates Notch-Dependent Lineage Specification during Drosophila Hematopoiesis
inferredcites →https://doi.org/10.1016/j.devcel.2009.03.003openalex-snapshot
Dual Role of Wingless Signaling in Stem-like Hematopoietic Precursor Maintenance in Drosophila
inferredcites →https://doi.org/10.1016/j.devcel.2015.03.014openalex-snapshot
Active Hematopoietic Hubs in Drosophila Adults Generate Hemocytes and Contribute to Immune Response
inferredcites →https://doi.org/10.1016/j.exphem.2014.06.002openalex-snapshot
Drosophila as a model for the two myeloid blood cell systems in vertebrates
inferredcites →https://doi.org/10.1016/j.stem.2010.07.015openalex-snapshot
Early B Cell Factor 2 Regulates Hematopoietic Stem Cell Homeostasis in a Cell-Nonautonomous Manner
inferredcites →https://doi.org/10.1016/j.ydbio.2007.08.011openalex-snapshot
The Friend of GATA protein U-shaped functions as a hematopoietic tumor suppressor in Drosophila
inferredcites →https://doi.org/10.1016/j.ydbio.2010.08.003openalex-snapshot
Hematopoietic progenitors and hemocyte lineages in the Drosophila lymph gland
inferredcites →https://doi.org/10.1016/j.ydbio.2011.01.035openalex-snapshot
JAK/STAT and the GATA factor Pannier control hemocyte maturation and differentiation in Drosophila
inferredcites →https://doi.org/10.1016/j.ydbio.2013.04.004openalex-snapshot
Extracellular matrix-modulated Heartless signaling in Drosophila blood progenitors regulates their differentiation via a Ras/ETS/FOG pathway and target of rapamycin function
inferredcites →https://doi.org/10.1016/s0925-4773(01)00566-4openalex-snapshot
A P-insertion screen identifying novel X-linked essential genes in Drosophila
inferredcites →https://doi.org/10.1017/s0031182000065173openalex-snapshot
Insect immunity: early events in the encapsulation process of parasitoid ( Leptopilina boulardi ) eggs in resistant and susceptible strains of Drosophila
inferredcites →https://doi.org/10.1038/376263a0openalex-snapshot
Failure of B-cell differentiation in mice lacking the transcription factor EBF
inferredcites →https://doi.org/10.1038/embor.2008.170openalex-snapshot
Plasticity of Drosophila Stat DNA binding shows an evolutionary basis for Stat transcription factor preferences
inferredcites →https://doi.org/10.1038/embor.2011.223openalex-snapshot
Oxidative stress in the haematopoietic niche regulates the cellular immune response in Drosophila
inferredcites →https://doi.org/10.1038/nature05585openalex-snapshot
A Hedgehog- and Antennapedia-dependent niche maintains Drosophila haematopoietic precursors
inferredcites →https://doi.org/10.1038/nature05650openalex-snapshot
Control of blood cell homeostasis in Drosophila larvae by the posterior signalling centre
inferredcites →https://doi.org/10.1038/nature08313openalex-snapshot
Reactive oxygen species prime Drosophila haematopoietic progenitors for differentiation
inferredcites →https://doi.org/10.1038/ng1404openalex-snapshot
Evidence for a fruit fly hemangioblast and similarities between lymph-gland hematopoiesis in fruit fly and mammal aorta-gonadal-mesonephros mesoderm
inferredcites →https://doi.org/10.1073/pnas.0611511104openalex-snapshot
An optimized transgenesis system for Drosophila using germ-line-specific φC31 integrases
inferredcites →https://doi.org/10.1073/pnas.1109407109openalex-snapshot
Size control of the Drosophila hematopoietic niche by bone morphogenetic protein signaling reveals parallels with mammals
inferredcites →https://doi.org/10.1073/pnas.1303559111openalex-snapshot
ARF1–GTP regulates Asrij to provide endocytic control of Drosophila blood cell homeostasis
inferredcites →https://doi.org/10.1073/pnas.1423967112openalex-snapshot
The EBF transcription factor Collier directly promotes Drosophila blood cell progenitor maintenance independently of the niche
inferredcites →https://doi.org/10.1101/gad.1052803openalex-snapshot
A Serrate-expressing signaling center controls Drosophila hematopoiesis
inferredcites →https://doi.org/10.1101/gad.1602607openalex-snapshot
The hematopoietic stem cell and its niche: a comparative view
inferredcites →https://doi.org/10.1101/gad.187328.112openalex-snapshot
Transcription factor Ebf1 regulates differentiation stage-specific signaling, proliferation, and survival of B cells
inferredcites →https://doi.org/10.1111/j.1462-5822.2004.00462.xopenalex-snapshot
New insights into Drosophila larval haemocyte functions through genome-wide analysis
inferredcites →https://doi.org/10.1126/science.1199643openalex-snapshot
Interaction Between Notch and Hif-α in Development and Survival of Drosophila Blood Cells
inferredcites →https://doi.org/10.1159/000353765openalex-snapshot
The Role of Hemocytes in Anopheles gambiae Antiplasmodial Immunity
inferredcites →https://doi.org/10.1186/1471-2148-8-131openalex-snapshot
The metazoan history of the COE transcription factors. Selection of a variant HLH motif by mandatory inclusion of a duplicated exon in vertebrates
inferredcites →https://doi.org/10.1242/dev.01837openalex-snapshot
TheDrosophilalymph gland as a developmental model of hematopoiesis
inferredcites →https://doi.org/10.1242/dev.043943openalex-snapshot
Hematopoietic stem cells in Drosophila
inferredcites →https://doi.org/10.1242/dev.053728openalex-snapshot
Serpent, Suppressor of Hairless and U-shaped are crucial regulators of hedgehog niche expression and prohemocyte maintenance during Drosophila larval hematopoiesis
inferredcites →https://doi.org/10.1242/dev.069336openalex-snapshot
Germ line differentiation factor Bag of Marbles is a regulator of hematopoietic progenitor maintenance during Drosophila hematopoiesis
inferredcites →https://doi.org/10.1242/dev.074203openalex-snapshot
Multifaceted roles of PTEN and TSC orchestrate growth and differentiation of Drosophila blood progenitors
inferredcites →https://doi.org/10.1242/dev.079087openalex-snapshot
Nutritional regulation of stem and progenitor cells in Drosophila
inferredcites →https://doi.org/10.1242/dev.080259openalex-snapshot
Dual role for Insulin/TOR signaling in the control of hematopoietic progenitor maintenance in Drosophila
inferredcites →https://doi.org/10.1242/dev.121798openalex-snapshot
Bag of Marbles controls the size and organization of the Drosophila hematopoietic niche through interactions with the Insulin-like growth factor pathway and Retinoblastoma-family protein
inferredcites →https://doi.org/10.1242/dmm.007351openalex-snapshot
Drosophila: a model for studying genetic and molecular aspects of haematopoiesis and associated leukaemias
inferredcites →https://doi.org/10.1371/journal.pbio.0020196openalex-snapshot
Cellular Immune Response to Parasitization in Drosophila Requires the EBF Orthologue Collier
inferredcites →https://doi.org/10.1371/journal.pbio.1000441openalex-snapshot
A Short Receptor Downregulates JAK/STAT Signalling to Control the Drosophila Cellular Immune Response
inferredcites →https://doi.org/10.1371/journal.pone.0041604openalex-snapshot
Gene Regulatory Networks Controlling Hematopoietic Progenitor Niche Cell Production and Differentiation in the Drosophila Lymph Gland
inferredcites →https://doi.org/10.1371/journal.pone.0074684openalex-snapshot
Drosophila E-Cadherin Functions in Hematopoietic Progenitors to Maintain Multipotency and Block Differentiation
inferredcites →https://doi.org/10.1371/journal.pone.0107768openalex-snapshot
Antioxidants Maintain E-Cadherin Levels to Limit Drosophila Prohemocyte Differentiation
inferredcites →https://doi.org/10.1387/ijdb.093053jkopenalex-snapshot
Ontogeny of the Drosophila larval hematopoietic organ, hemocyte homeostasis and the dedicated cellular immune response to parasitism
inferredcites →https://doi.org/10.4161/cc.6.12.4370openalex-snapshot
The hematopoietic niche: a Drosophila model, at last.
inferredcites →https://doi.org/10.7554/elife.03626openalex-snapshot
Pvr expression regulators in equilibrium signal control and maintenance of Drosophila blood progenitors

What points at this work

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

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inferred← citeshttps://doi.org/10.1002/1873-3468.12327openalex-snapshot
Drosophila hematopoiesis under normal conditions and in response to immune stress
inferred← citeshttps://doi.org/10.1002/dvg.23210openalex-snapshot
The mir‐7 and bag of marbles genes regulate Hedgehog pathway signaling in blood cell progenitors in Drosophila larval lymph glands
inferred← citeshttps://doi.org/10.1007/978-981-13-0529-0_11openalex-snapshot
From Drosophila Blood Cells to Human Leukemia
inferred← citeshttps://doi.org/10.1016/j.cub.2017.08.019openalex-snapshot
Novel Organelles with Elements of Bacterial and Eukaryotic Secretion Systems Weaponize Parasites of Drosophila
inferred← citeshttps://doi.org/10.1016/j.cub.2021.08.027openalex-snapshot
A gap-junction-mediated, calcium-signaling network controls blood progenitor fate decisions in hematopoiesis
inferred← citeshttps://doi.org/10.1016/j.dci.2017.11.017openalex-snapshot
The Drosophila lymph gland is an ideal model for studying hematopoiesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.02.013openalex-snapshot
S-nitrosylation-triggered unfolded protein response maintains hematopoietic progenitors in Drosophila
inferred← citeshttps://doi.org/10.1016/j.devcel.2024.05.023openalex-snapshot
Wnt signaling couples G2 phase control with differentiation during hematopoiesis in Drosophila
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2022.10.002openalex-snapshot
ROS-directed activation of Toll/NF-κB in the hematopoietic niche triggers benzene-induced emergency hematopoiesis
inferred← citeshttps://doi.org/10.1016/j.ibmb.2021.103584openalex-snapshot
Proteomics of purified lamellocytes from Drosophila melanogaster HopT identifies new membrane proteins and networks involved in their functions
inferred← citeshttps://doi.org/10.1016/j.jgg.2024.11.001openalex-snapshot
Rab1 and Syntaxin 17 regulate hematopoietic homeostasis through β-integrin trafficking in Drosophila
inferred← citeshttps://doi.org/10.1016/j.smim.2016.03.010openalex-snapshot
Macrophages and cellular immunity in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.ydbio.2016.11.003openalex-snapshot
Human NUP98-HOXA9 promotes hyperplastic growth of hematopoietic tissues in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ydbio.2018.06.020openalex-snapshot
Hedgehog signaling from the Posterior Signaling Center maintains U-shaped expression and a prohemocyte population in Drosophila
inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.03.018openalex-snapshot
Context-specific functions of Notch in Drosophila blood cell progenitors
inferred← citeshttps://doi.org/10.1016/j.ydbio.2024.10.004openalex-snapshot
Novel features of Drosophila hematopoiesis uncovered by long-term live imaging
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.08.010openalex-snapshot
Notch-regulated hematopoiesis in Drosophila: Parallels and contrasts with vertebrate blood development
inferred← citeshttps://doi.org/10.1038/ncomms11634openalex-snapshot
Vascular control of the Drosophila haematopoietic microenvironment by Slit/Robo signalling
inferred← citeshttps://doi.org/10.1038/s41467-020-18135-yopenalex-snapshot
Single-cell transcriptome maps of myeloid blood cell lineages in Drosophila
inferred← citeshttps://doi.org/10.1038/s41467-025-60493-yopenalex-snapshot
Serotonergic neurons regulate the Drosophila vascular niche to control immune stress hematopoiesis
inferred← citeshttps://doi.org/10.1073/pnas.2217862120openalex-snapshot
A mechanosensitive vascular niche for Drosophila hematopoiesis
inferred← citeshttps://doi.org/10.1073/pnas.2303018120openalex-snapshot
Maintenance of hematopoietic stem cell niche homeostasis requires gap junction–mediated calcium signaling
inferred← citeshttps://doi.org/10.1101/2023.06.29.547151openalex-snapshot
Wnt Signaling Couples G2 Phase Control with Differentiation During Hematopoiesis
inferred← citeshttps://doi.org/10.1101/2023.06.30.547214openalex-snapshot
S-nitrosylation-mediated unfolded protein response maintains hematopoietic progenitors
inferred← citeshttps://doi.org/10.1101/2025.03.03.641076openalex-snapshot
Sex differences in the regulation and function of cellular immunity in Drosophila
inferred← citeshttps://doi.org/10.1111/febs.17288openalex-snapshot
Atg2 controls Drosophila hematopoiesis through the PVR / TOR signaling pathways
inferred← citeshttps://doi.org/10.1111/imm.13390openalex-snapshot
Haemocyte‐mediated immunity in insects: Cells, processes and associated components in the fight against pathogens and parasites
inferred← citeshttps://doi.org/10.1128/9781555819194.ch5openalex-snapshot
Advances in Myeloid-Like Cell Origins and Functions in the Model OrganismDrosophila melanogaster
inferred← citeshttps://doi.org/10.1128/microbiolspec.mchd-0038-2016openalex-snapshot
Advances in Myeloid-Like Cell Origins and Functions in the Model OrganismDrosophila melanogaster
inferred← citeshttps://doi.org/10.1242/dev.149641openalex-snapshot
The matrix protein Tiggrin regulates plasmatocyte maturation inDrosophilalarva
inferred← citeshttps://doi.org/10.1242/dev.185645openalex-snapshot
Alary muscles and thoracic alary-related muscles are atypical striated muscles involved in maintaining the position of internal organs
inferred← citeshttps://doi.org/10.1242/dev.200216openalex-snapshot
Intermediate progenitor cells provide a transition between hematopoietic progenitors and their differentiated descendants
inferred← citeshttps://doi.org/10.1242/dev.201767openalex-snapshot
Single-cell transcriptomics identifies new blood cell populations in Drosophila released at the onset of metamorphosis
inferred← citeshttps://doi.org/10.1242/dev.204367openalex-snapshot
The matrix glycoprotein Papilin maintains the haematopoietic progenitor pool in Drosophila lymph glands
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009709openalex-snapshot
Ubx-Collier signaling cascade maintains blood progenitors in the posterior lobes of the Drosophila larval lymph gland
inferred← citeshttps://doi.org/10.1371/journal.pgen.1011448openalex-snapshot
Dual role for Headcase in hemocyte progenitor fate determination in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1371/journal.pgen.1012151openalex-snapshot
Sex differences in the regulation and function of cellular immunity in Drosophila
inferred← citeshttps://doi.org/10.1371/journal.ppat.1009615openalex-snapshot
A parasitoid wasp of Drosophila employs preemptive and reactive strategies to deplete its host’s blood cells
inferred← citeshttps://doi.org/10.14232/phd.10133openalex-snapshot
A Headcase a Drosophila melanogaster vérsejtképződésének szabályozó faktora
inferred← citeshttps://doi.org/10.14232/phd.12144openalex-snapshot
Characterizing the dual role of Headcase in hemocyte progenitor maintenance in Drosophila melanogaster
inferred← citeshttps://doi.org/10.14348/molcells.2022.2039openalex-snapshot
Intrinsic and Extrinsic Regulation of Hematopoiesis in Drosophila
inferred← citeshttps://doi.org/10.1534/g3.116.034439openalex-snapshot
Screening and Analysis of Janelia FlyLight Project Enhancer-Gal4 Strains Identifies Multiple Gene Enhancers Active During Hematopoiesis in Normal and Wasp-ChallengedDrosophilaLarvae
inferred← citeshttps://doi.org/10.1534/genetics.118.300223openalex-snapshot
Drosophila as a Genetic Model for Hematopoiesis
inferred← citeshttps://doi.org/10.1534/genetics.119.302209openalex-snapshot
Cell Adhesion-Mediated Actomyosin Assembly Regulates the Activity of Cubitus Interruptus for Hematopoietic Progenitor Maintenance in Drosophila
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1326573/v1openalex-snapshot
A mechanosensitive vascular niche for Drosophila hematopoiesis
inferred← citeshttps://doi.org/10.32607/actanaturae.27410openalex-snapshot
Molecular Mechanisms of Drosophila Hematopoiesis
inferred← citeshttps://doi.org/10.3389/fcell.2020.00382openalex-snapshot
The Posterior Signaling Center Is an Important Microenvironment for Homeostasis of the Drosophila Lymph Gland
inferred← citeshttps://doi.org/10.3389/fcell.2021.739357openalex-snapshot
Characterization of the Drosophila Adult Hematopoietic System Reveals a Rare Cell Population With Differentiation and Proliferation Potential
inferred← citeshttps://doi.org/10.3389/fcell.2022.834720openalex-snapshot
Identification of Bipotential Blood Cell/Nephrocyte Progenitors in Drosophila: Another Route for Generating Blood Progenitors
inferred← citeshttps://doi.org/10.3389/fimmu.2021.719349openalex-snapshot
Drosophila as a Model to Study Cellular Communication Between the Hematopoietic Niche and Blood Progenitors Under Homeostatic Conditions and in Response to an Immune Stress
inferred← citeshttps://doi.org/10.3389/fimmu.2025.1641695openalex-snapshot
A novel role for Hsc70–4 in blood cell differentiation in Drosophila
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1824544openalex-snapshot
Niche-derived exosomes control Drosophila immune stress hematopoiesis
inferred← citeshttps://doi.org/10.3389/fphys.2019.00603openalex-snapshot
Drosophila Cellular Immunity Against Parasitoid Wasps: A Complex and Time-Dependent Process
inferred← citeshttps://doi.org/10.3390/genes10030173openalex-snapshot
Headcase is a Repressor of Lamellocyte Fate in Drosophila melanogaster
inferred← citeshttps://doi.org/10.3390/ijms21155246openalex-snapshot
Regulation of Drosophila Hematopoiesis in Lymph Gland: From a Developmental Signaling Point of View
inferred← citeshttps://doi.org/10.3390/ijms23147767openalex-snapshot
Peeling Back the Layers of Lymph Gland Structure and Regulation
inferred← citeshttps://doi.org/10.70675/01385ba5z45e1z4271zb120z157ed7ca0382openalex-snapshot
Functional characterization of alternative splice variants of the Drosophila GATA transcription factor serpent containing either one or two zinc finger domains
inferred← citeshttps://doi.org/10.70675/0c0f818fz10b0z42d5zbea1zde77534d9ffaopenalex-snapshot
Etude du rôle et des modes d’action de l’enzyme épigénétique TET chez la drosophile
inferred← citeshttps://doi.org/10.70675/40ceb130zff93z4c31z9cc6zefc959685afaopenalex-snapshot
Régulation de l'hématopoïèse par les facteurs de transcription de type GATA et FOG chez la drosophile
inferred← citeshttps://doi.org/10.70675/7885ab1bz7ce4z4968z92a8zee428bb0133bopenalex-snapshot
The control of hematopoiesis under normal and immune stress condition : insights from Drosophila
inferred← citeshttps://doi.org/10.70675/a9c50a3dz0d5dz4f46za05cz9b5fe715b7e1openalex-snapshot
Rôle du système vasculaire dans le contrôle de l'hématopoïèse chez la drosophile : étude de la voie de signalisation fibroblast growth factor
inferred← citeshttps://doi.org/10.70675/aaeb2f3cz660az4540z82e9z6ccf1938a8feopenalex-snapshot
Characterization of the Lysine Acetyltransferase dmMOZ function and mode of action during Drosophila hematopoiesis
inferred← citeshttps://doi.org/10.70675/e22450c4z6ee9z49eczabdcz080f041eecd8openalex-snapshot
Mise en place de l'identité musculaire durant la myogenèse embryonnaire chez la drosophile
inferred← citeshttps://doi.org/10.70675/f82dd074za47dz49bcz9a99z228e03c574efopenalex-snapshot
Drosophila immune response to the endoparasitoid wasp Leptopilina boulardi : characterization of a resistance reaction
inferred← citeshttps://doi.org/10.7554/elife.25094openalex-snapshot
Dual role for Jumu in the control of hematopoietic progenitors in the Drosophila lymph gland
inferred← citeshttps://doi.org/10.7554/elife.25496openalex-snapshot
Reactive oxygen species-dependent Toll/NF-κB activation in the Drosophila hematopoietic niche confers resistance to wasp parasitism
inferred← citeshttps://doi.org/10.7554/elife.28081openalex-snapshot
Modulation of occluding junctions alters the hematopoietic niche to trigger immune activation
inferred← citeshttps://doi.org/10.7554/elife.64672openalex-snapshot
The vascular niche controls Drosophila hematopoiesis via fibroblast growth factor signaling
inferred← citeshttps://doi.org/10.7554/elife.67516openalex-snapshot
Paths and pathways that generate cell-type heterogeneity and developmental progression in hematopoiesis
inferred← citeshttps://doi.org/10.7554/elife.78906openalex-snapshot
Hematopoietic plasticity mapped in Drosophila and other insects
inferred← citeshttps://doi.org/10.7554/elife.84085openalex-snapshot
Kinetics of blood cell differentiation during hematopoiesis revealed by quantitative long-term live imaging
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