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The cell-mediated immunity of Drosophila melanogaster: Hemocyte lineages, immune compartments, microanatomy and regulation

https://doi.org/10.1016/j.dci.2013.06.005

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What this work says

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

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Odd‐skipped maintains prohemocyte potency and blocks blood cell development in Drosophila

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Transcriptional regulation of eater gene expression in Drosophila blood cells

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The Dorothy enhancer has tinman binding sites and drives hopscotch‐induced tumor formation

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The immune response in Drosophila: pattern of cecropin expression and biological activity.

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Cloning, Structure, Cellular Localization, and Possible Function of the Tumor Suppressor Gene lethal(3)malignant blood neoplasm-1 of Drosophila melanogaster

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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

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Comparative study of structure and function of blood cells from two Drosophila species

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Basement membrane abnormalities in melanotic tumor formation ofDrosophila

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Drosophila tumors and the structure of larval lymph glands

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Lamellocyte differentiation in Drosophila larvae parasitized by Leptopilina

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Signal transduction pathways, intrinsic regulators, and the control of cell fate choice

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Eater, a Transmembrane Protein Mediating Phagocytosis of Bacterial Pathogens in Drosophila

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Six-Microns-Under Acts Upstream of Draper in the Glial Phagocytosis of Apoptotic Neurons

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Interaction between Differentiating Cell- and Niche-Derived Signals in Hematopoietic Progenitor Maintenance

inferredcites →https://doi.org/10.1016/j.cub.2006.11.026openalex-snapshot

Psidin Is Required in Drosophila Blood Cells for Both Phagocytic Degradation and Immune Activation of the Fat Body

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Nimrod, a Putative Phagocytosis Receptor with EGF Repeats in Drosophila Plasmatocytes

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The PDGF/VEGF Receptor Controls Blood Cell Survival in Drosophila

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.exger.2011.07.004openalex-snapshot

Senescence of the cellular immune response in Drosophila melanogaster

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Syndecan‐dependent binding of Drosophila hemocytes to laminin α3/5 chain LG4‐5 modules: potential role in sessile hemocyte islets formation

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A RhoGAP protein as a main immune suppressive factor in the Leptopilina boulardi (Hymenoptera, Figitidae)–Drosophila melanogaster interaction

inferredcites →https://doi.org/10.1016/j.imlet.2005.03.021openalex-snapshot

Sterile wounding is a minimal and sufficient trigger for a cellular immune response in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.imlet.2009.08.004openalex-snapshot

In vivo detection of lamellocytes in Drosophila melanogaster

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

Expression pattern of Filamin-240 in Drosophila blood cells

inferredcites →https://doi.org/10.1016/j.molimm.2010.04.017openalex-snapshot

Cell lineage tracing reveals the plasticity of the hemocyte lineages and of the hematopoietic compartments in Drosophila melanogaster

inferredcites →https://doi.org/10.1016/j.ydbio.2003.06.001openalex-snapshot

Drosophila hemolectin gene is expressed in embryonic and larval hemocytes and its knock down causes bleeding defects

inferredcites →https://doi.org/10.1016/j.ydbio.2006.04.455openalex-snapshot

Regulation of Drosophila Friend of GATA gene, u-shaped, during hematopoiesis: A direct role for Serpent and Lozenge

inferredcites →https://doi.org/10.1016/j.ydbio.2007.03.010openalex-snapshot

A GATA/RUNX cis-regulatory module couples Drosophila blood cell commitment and differentiation into crystal cells

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/s0960-9822(00)00569-8openalex-snapshot

Interactions between the cellular and humoral immune responses in Drosophila

inferredcites →https://doi.org/10.1016/s1074-7613(00)80410-0openalex-snapshot

Croquemort, A Novel Drosophila Hemocyte/Macrophage Receptor that Recognizes Apoptotic Cells

inferredcites →https://doi.org/10.1016/s1534-5807(03)00335-6openalex-snapshot

Thicker Than Blood

inferredcites →https://doi.org/10.1038/embor.2011.238openalex-snapshot

Immune cell transdifferentiation: a complex crosstalk between circulating immune cells and the haematopoietic niche

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/ncb2063openalex-snapshot

RhoL controls invasion and Rap1 localization during immune cell transmigration in Drosophila

inferredcites →https://doi.org/10.1038/ncb2453openalex-snapshot

Direct sensing of systemic and nutritional signals by haematopoietic progenitors in Drosophila

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/10.1038/nmeth.1356openalex-snapshot

G-TRACE: rapid Gal4-based cell lineage analysis in Drosophila

inferredcites →https://doi.org/10.1073/pnas.0403789101openalex-snapshot

A directed screen for genes involved in Drosophila blood cell activation

inferredcites →https://doi.org/10.1073/pnas.0436940100openalex-snapshot

Hemese, a hemocyte-specific transmembrane protein, affects the cellular immune response in Drosophila

inferredcites →https://doi.org/10.1073/pnas.0709951105openalex-snapshot

Circulating blood cells function as a surveillance system for damaged tissue in Drosophila larvae

inferredcites →https://doi.org/10.1073/pnas.0801766106openalex-snapshot

Sessile hemocytes as a hematopoietic compartment in Drosophila melanogaster

inferredcites →https://doi.org/10.1073/pnas.0903971106openalex-snapshot

Elimination of plasmatocytes by targeted apoptosis reveals their role in multiple aspects of the Drosophila immune response

inferredcites →https://doi.org/10.1073/pnas.131215798openalex-snapshot

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inferredcites →https://doi.org/10.1073/pnas.95.24.14337openalex-snapshot

Analysis of the Drosophila host defense in domino mutant larvae, which are devoid of hemocytes

inferredcites →https://doi.org/10.1074/jbc.m110.204503openalex-snapshot

Integrin βν-mediated Phagocytosis of Apoptotic Cells in Drosophila Embryos

inferredcites →https://doi.org/10.1074/jbc.m110.214007openalex-snapshot

Recognition of Pathogenic Microbes by the Drosophila Phagocytic Pattern Recognition Receptor Eater

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inferredcites →https://doi.org/10.1074/jbc.m408597200openalex-snapshot

Draper-mediated and Phosphatidylserine-independent Phagocytosis of Apoptotic Cells by Drosophila Hemocytes/Macrophages

inferredcites →https://doi.org/10.1083/jcb.200405120openalex-snapshot

Live imaging of wound inflammation in Drosophila embryos reveals key roles for small GTPases during in vivo cell migration

inferredcites →https://doi.org/10.1083/jcb.200508161openalex-snapshot

Distinct mechanisms regulate hemocyte chemotaxis during development and wound healing in Drosophila melanogaster

inferredcites →https://doi.org/10.1083/jcb.5.2.235openalex-snapshot

Functional Significance of the Crystal Cells in the Larva of Drosophila melanogaster

inferredcites →https://doi.org/10.1093/emboj/cdg622openalex-snapshot

Cooperation between the GATA and RUNX factors Serpent and Lozenge during Drosophila hematopoiesis

inferredcites →https://doi.org/10.1093/genetics/162.3.1259openalex-snapshot

Regulation of Larval Hematopoiesis in Drosophila melanogaster: A Role for the multi sex combs Gene

inferredcites →https://doi.org/10.1093/genetics/163.1.203openalex-snapshot

Analysis of Ras-Induced Overproliferation in Drosophila Hemocytes

inferredcites →https://doi.org/10.1093/molbev/msn180openalex-snapshot

Evolution of Genes and Repeats in the Nimrod Superfamily

inferredcites →https://doi.org/10.1101/gad.1052803openalex-snapshot

A Serrate-expressing signaling center controls Drosophila hematopoiesis

inferredcites →https://doi.org/10.1111/j.1365-2443.2005.00883.xopenalex-snapshot

Drosophila melanogaster Rac2 is necessary for a proper cellular immune response

inferredcites →https://doi.org/10.1111/j.1440-169x.1982.00083.xopenalex-snapshot

Ultrastructure and Cytochemistry of the Cell-types in the Tumorous Hematopoietic Organs and the Hemolymph of the Mutant Lethal (1) Malignant Blood Neoplasm (l(1)mbn) of Drosophila Melanogaster. (drosophila/mutant blood cells/ultrastructure/cytochemistry)

inferredcites →https://doi.org/10.1126/science.284.5422.1991openalex-snapshot

Requirement for Croquemort in Phagocytosis of Apoptotic Cells in Drosophila

inferredcites →https://doi.org/10.1126/science.288.5463.146openalex-snapshot

Specification of Drosophila Hematopoietic Lineage by Conserved Transcription Factors

inferredcites →https://doi.org/10.1128/mcb.01239-08openalex-snapshot

Requirement of Split ends for Epigenetic Regulation of Notch Signal-Dependent Genes during Infection-Induced Hemocyte Differentiation

inferredcites →https://doi.org/10.1159/000210264openalex-snapshot

Genetic Ablation of Drosophila Phagocytes Reveals Their Contribution to Both Development and Resistance to Bacterial Infection

inferredcites →https://doi.org/10.1186/1471-213x-10-65openalex-snapshot

An in vivo RNA interference screen identifies gene networks controlling Drosophila melanogasterblood cell homeostasis

inferredcites →https://doi.org/10.1242/dev.00702openalex-snapshot

The two origins of hemocytes in Drosophila

inferredcites →https://doi.org/10.1242/dev.01837openalex-snapshot

TheDrosophilalymph gland as a developmental model of hematopoiesis

inferredcites →https://doi.org/10.1242/dev.02034openalex-snapshot

Resolving embryonic blood cell fate choice in Drosophila :interplay of GCM and RUNX factors

inferredcites →https://doi.org/10.1242/dev.036517openalex-snapshot

Fascin is required for blood cell migration during Drosophilaembryogenesis

inferredcites →https://doi.org/10.1242/dev.046797openalex-snapshot

Interdependence of macrophage migration and ventral nerve cord development in Drosophila embryos

inferredcites →https://doi.org/10.1242/dev.067322openalex-snapshot

The peripheral nervous system supports blood cell homing and survival in the Drosophila larva

inferredcites →https://doi.org/10.1242/dev.086785openalex-snapshot

Notch cooperates with Lozenge/Runx to lock haemocytes into a differentiation programme

inferredcites →https://doi.org/10.1242/dev.118.2.401openalex-snapshot

Targeted gene expression as a means of altering cell fates and generating dominant phenotypes

inferredcites →https://doi.org/10.1242/dmm.000950openalex-snapshot

An innate immune response of blood cells to tumors and tissue damage in Drosophila

inferredcites →https://doi.org/10.1242/dmm.005694openalex-snapshot

Ena drives invasive macrophage migration in Drosophila embryos

inferredcites →https://doi.org/10.1242/jcs.021931openalex-snapshot

Haemocyte-derived SPARC is required for collagen-IV-dependent stability of basal laminae in Drosophila embryos

inferredcites →https://doi.org/10.1242/jcs.03420openalex-snapshot

Crystal cell rupture after injury in Drosophila requires the JNK pathway, small GTPases and the TNF homolog Eiger

inferredcites →https://doi.org/10.1242/jcs.114462openalex-snapshot

The actin cross-linker Filamin/Cheerio mediates tumor malignancy downstream of JNK signaling

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.0014051openalex-snapshot

Lineage Tracing of Lamellocytes Demonstrates Drosophila Macrophage Plasticity

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/10.1534/genetics.106.061978openalex-snapshot

Melanotic Mutants in Drosophila: Pathways and Phenotypes

inferredcites →https://doi.org/10.1534/genetics.108.089094openalex-snapshot

A Misexpression Screen to Identify Regulators of Drosophila Larval Hemocyte Development

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Genetic Analysis of Contributions of Dorsal Group and JAK-Stat92E Pathway Genes to Larval Hemocyte Concentration and the Egg Encapsulation Response in Drosophila

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Definition ofDrosophilahemocyte subsets by cell-type specific antigens

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Hydrogen Peroxide Production in Immune-Reactive Drosophila melanogaster

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Drosophila Nimrod proteins bind bacteria

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Of blood cells and the nervous system

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Role of NPxY motif in Draper-mediated apoptotic cell clearance in Drosophila

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

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inferred← citeshttps://doi.org/10.1016/j.mod.2017.04.004openalex-snapshot

Comparative analysis of gene expression profiles for several migrating cell types identifies cell migration regulators

inferred← citeshttps://doi.org/10.1016/j.mod.2018.08.003openalex-snapshot

An in vitro method for studying subcellular rearrangements during cell polarization in Drosophila melanogaster hemocytes

inferred← citeshttps://doi.org/10.1016/j.molimm.2019.03.008openalex-snapshot

The prophenoloxidase system in Drosophila participates in the anti-nematode immune response

inferred← citeshttps://doi.org/10.1016/j.molimm.2020.02.007openalex-snapshot

A novel WSSV responsive plasma protein from Litopenaeus vannamei contributes to hemocytes anti-apoptosis

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.2019.06.006openalex-snapshot

Pericardin, a Drosophila collagen, facilitates accumulation of hemocytes at the heart

inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.08.008openalex-snapshot

SETDB1 modulates the differentiation of both the crystal cells and the lamellocytes in Drosophila

inferred← citeshttps://doi.org/10.1016/j.ydbio.2020.10.006openalex-snapshot

There and back again: The mechanisms of differentiation and transdifferentiation in Drosophila blood cells

inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.07.014openalex-snapshot

Taking damage as an advantage: Adaptation of Drosophila hemocyte functions upon DNA damage

inferred← citeshttps://doi.org/10.1016/j.ymeth.2014.02.038openalex-snapshot

Drosophila hematopoiesis: Markers and methods for molecular genetic analysis

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/s41467-021-22866-xopenalex-snapshot

Regression plane concept for analysing continuous cellular processes with machine learning

inferred← citeshttps://doi.org/10.1038/s41598-017-15940-2openalex-snapshot

Drosophila muscles regulate the immune response against wasp infection via carbohydrate metabolism

inferred← citeshttps://doi.org/10.1038/s41598-020-80355-5openalex-snapshot

The preference of Trichopria drosophilae for pupae of Drosophila suzukii is independent of host size

inferred← citeshttps://doi.org/10.1038/s42003-020-0775-xopenalex-snapshot

Trypanosomatid parasite dynamically changes the transcriptome during infection and modifies honey bee physiology

inferred← citeshttps://doi.org/10.1073/pnas.1900147116openalex-snapshot

Chemical depletion of phagocytic immune cells in Anopheles gambiae reveals dual roles of mosquito hemocytes in anti- Plasmodium immunity

inferred← citeshttps://doi.org/10.1073/pnas.2017460118openalex-snapshot

Extracellular matrix protein N-glycosylation mediates immune self-tolerance in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1073/pnas.2535199123openalex-snapshot

A gustatory receptor–Akt axis couples nutrient sensing to hematopoiesis in the silkworm

inferred← citeshttps://doi.org/10.1074/mcp.m116.060723openalex-snapshot

Molecular Profiling of Phagocytic Immune Cells in Anopheles gambiae Reveals Integral Roles for Hemocytes in Mosquito Innate Immunity

inferred← citeshttps://doi.org/10.1079/978178924881.0003openalex-snapshot

Entomopathogenic Nematodes as a Model for Probing the Insect Immune System

inferred← citeshttps://doi.org/10.1079/9781789248814.0003openalex-snapshot

Entomopathogenic Nematodes as a Model for Probing the Insect Immune System

inferred← citeshttps://doi.org/10.1079/9781800620322.0003openalex-snapshot

Insect Innate Immunity against Entomopathogenic Nematodes

inferred← citeshttps://doi.org/10.1080/19336934.2016.1182269openalex-snapshot

Tissue communication in a systemic immune response ofDrosophila

inferred← citeshttps://doi.org/10.1080/21505594.2020.1838116openalex-snapshot

Parasitoid wasp venom vesicles (venosomes) enter Drosophila melanogaster lamellocytes through a flotillin/lipid raft-dependent endocytic pathway

inferred← citeshttps://doi.org/10.1080/21505594.2021.1980989openalex-snapshot

Deciphering of Candida parapsilosis induced immune response in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1093/gbe/evaa075openalex-snapshot

Differential Expression of Immune Genes between Two Closely Related Beetle Species with Different Immunocompetence following Attack by Asecodes parviclava

inferred← citeshttps://doi.org/10.1093/gbe/evag034openalex-snapshot

Predictors of Protein Evolution in the drosophilid Immune System

inferred← citeshttps://doi.org/10.1093/genetics/iyag208openalex-snapshot

A hybrid transcriptome assembly reveals coding and noncoding landscapes in Drosophila hemocytes

inferred← citeshttps://doi.org/10.1093/icb/icv021openalex-snapshot

Integrated Immune and Cardiovascular Function in Pancrustacea: Lessons from the Insects

inferred← citeshttps://doi.org/10.1093/icb/icv094openalex-snapshot

Respiratory and Metabolic Impacts of Crustacean Immunity: Are there Implications for the Insects?

inferred← citeshttps://doi.org/10.1096/fj.201700296ropenalex-snapshot

Proprotein convertase Furin1 expression in the Drosophila fat body is essential for a normal antimicrobial peptide response and bacterial host defense

inferred← citeshttps://doi.org/10.1101/2020.05.26.086140openalex-snapshot

Rala and the exocyst control Pvr trafficking and signaling to ensure lymph gland homeostasis in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1101/2020.06.10.144584openalex-snapshot

Multi-Dimensional Immuno-Profiling of Drosophila Hemocytes by Single Cell Mass Cytometry

inferred← citeshttps://doi.org/10.1101/2021.03.13.435227openalex-snapshot

A Creb3-Like Transcription Factor Coordinates ER Function upon Food Intake to Regulate Lipid Metabolism

inferred← citeshttps://doi.org/10.1101/2021.11.19.469298openalex-snapshot

Loss of self-tolerance leads to altered gene expression and IMD pathway activation in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1101/2022.06.28.497890openalex-snapshot

Recognition of non-self is necessary to activate Drosophila ’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.1101/2024.05.29.596511openalex-snapshot

Retracing the horizontal transfer of a novel innate immune factor in Drosophila

inferred← citeshttps://doi.org/10.1101/2025.07.03.662979openalex-snapshot

Disruption of hemocyte differentiation and distribution in Drosophila Ptr 23c mutants

inferred← citeshttps://doi.org/10.1101/324335openalex-snapshot

Detection of immune system activation in hemolymph of Drosophila larvae exposed to chitosan-coated magnetite nanoparticles

inferred← citeshttps://doi.org/10.1101/648626openalex-snapshot

Metabolic adjustment of Drosophila hemocyte number and sessility by an adipokine

inferred← citeshttps://doi.org/10.1111/1365-2656.12579openalex-snapshot

Geographic variation and trade‐offs in parasitoid virulence

inferred← citeshttps://doi.org/10.1111/1748-5967.12384openalex-snapshot

JAK/STAT signaling in insect innate immunity

inferred← citeshttps://doi.org/10.1111/febs.15237openalex-snapshot

The adipokine NimrodB5 regulates peripheral hematopoiesis in Drosophila

inferred← citeshttps://doi.org/10.1111/imr.12647openalex-snapshot

Innate immune memory: An evolutionary perspective

inferred← citeshttps://doi.org/10.1111/pcmr.12590openalex-snapshot

Re‐evaluation of insect melanogenesis research: Views from the dark side

inferred← citeshttps://doi.org/10.1111/phen.12456openalex-snapshot

Population profile of haemocytes in the subcastes of the leaf‐cutter ant Atta sexdens (Hymenoptera: Formicidae) unveiled by flow cytometry

inferred← citeshttps://doi.org/10.1111/phen.70004openalex-snapshot

The effect of inactivated bacteria on the redox status of larvae of the wax moth Galleria mellonella

inferred← citeshttps://doi.org/10.1111/raq.12977openalex-snapshot

The Immune Priming in Aquaculture Invertebrates: Inspiration From Cellular Perspective and Future Investigation

inferred← citeshttps://doi.org/10.1111/sji.12170openalex-snapshot

JAK/STAT Pathway in Drosophila Immunity

inferred← citeshttps://doi.org/10.1128/iai.02318-14openalex-snapshot

Nitric Oxide Levels Regulate the Immune Response of Drosophila melanogaster Reference Laboratory Strains to Bacterial Infections

inferred← citeshttps://doi.org/10.1128/jvi.01985-19openalex-snapshot

Mitochondrial and Innate Immunity Transcriptomes from Spodoptera frugiperda Larvae Infected with the Spodoptera frugiperda Ascovirus

inferred← citeshttps://doi.org/10.1128/jvi.02320-14openalex-snapshot

Drosophila C Virus Systemic Infection Leads to Intestinal Obstruction

inferred← citeshttps://doi.org/10.1139/bcb-2018-0008openalex-snapshot

Phagocytosis: what’s on the menu?

inferred← citeshttps://doi.org/10.1146/annurev-genet-032425-100252openalex-snapshot

Multifaceted Defenses Against Parasitoid Wasps in Diptera

inferred← citeshttps://doi.org/10.1159/000502646openalex-snapshot

Cellular Immune Response Involving Multinucleated Giant Hemocytes with Two-Step Genome Amplification in the Drosophilid Zaprionus indianus

inferred← citeshttps://doi.org/10.1159/000520110openalex-snapshot

Broad Ultrastructural and Transcriptomic Changes Underlie the Multinucleated Giant Hemocyte Mediated Innate Immune Response against Parasitoids

inferred← citeshttps://doi.org/10.1186/s12915-016-0305-yopenalex-snapshot

Functional integration of the circulatory, immune, and respiratory systems in mosquito larvae: pathogen killing in the hemocyte-rich tracheal tufts

inferred← citeshttps://doi.org/10.1186/s12915-017-0408-0openalex-snapshot

Thioester-containing proteins regulate the Toll pathway and play a role in Drosophila defence against microbial pathogens and parasitoid wasps

inferred← citeshttps://doi.org/10.1186/s12915-024-01886-1openalex-snapshot

Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.1186/s13064-024-00185-3openalex-snapshot

Longitudinal tracking of hemocyte populations in vivo indicates lineage relationships and supports neural progenitor identity in adult neurogenesis

inferred← citeshttps://doi.org/10.1186/s13071-017-2302-6openalex-snapshot

Anopheles gambiae larvae mount stronger immune responses against bacterial infection than adults: evidence of adaptive decoupling in mosquitoes

inferred← citeshttps://doi.org/10.1242/bio.201410595openalex-snapshot

The Nimrod transmembrane receptor Eater is required for hemocyte attachment to the sessile compartment in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1242/dev.149641openalex-snapshot

The matrix protein Tiggrin regulates plasmatocyte maturation inDrosophilalarva

inferred← citeshttps://doi.org/10.1242/dmm.027102openalex-snapshot

A novel mode of induction of the humoral innate immune response in Drosophila larvae

inferred← citeshttps://doi.org/10.1242/dmm.038679openalex-snapshot

Enhancer of Polycomb and the Tip60 complex repress hematological tumor initiation by negatively regulating JAK/STAT pathway activity

inferred← citeshttps://doi.org/10.12688/f1000research.13117.1openalex-snapshot

The interplay between immunity and aging in Drosophila

inferred← citeshttps://doi.org/10.12688/wellcomeopenres.14560.1openalex-snapshot

Detecting proliferation of adult hemocytes in Drosophila by BrdU incorporation

inferred← citeshttps://doi.org/10.12688/wellcomeopenres.14560.2openalex-snapshot

Detecting proliferation of adult hemocytes in Drosophila by BrdU incorporation and PH3 expression in response to bacterial infection

inferred← citeshttps://doi.org/10.1371/journal.pbio.2006741openalex-snapshot

Simu-dependent clearance of dying cells regulates macrophage function and inflammation resolution

inferred← citeshttps://doi.org/10.1371/journal.pgen.1007052openalex-snapshot

dOCRL maintains immune cell quiescence by regulating endosomal traffic

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.pone.0159473openalex-snapshot

Genetic Screen in Drosophila Larvae Links ird1 Function to Toll Signaling in the Fat Body and Hemocyte Motility

inferred← citeshttps://doi.org/10.1371/journal.pone.0201573openalex-snapshot

Time-course analysis of Drosophila suzukii interaction with endoparasitoid wasps evidences a delayed encapsulation response compared to D. melanogaster

inferred← citeshttps://doi.org/10.1371/journal.ppat.1004067openalex-snapshot

Prophenoloxidase Activation Is Required for Survival to Microbial Infections in Drosophila

inferred← citeshttps://doi.org/10.1371/journal.ppat.1004895openalex-snapshot

Edin Expression in the Fat Body Is Required in the Defense Against Parasitic Wasps in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005746openalex-snapshot

Transdifferentiation and Proliferation in Two Distinct Hemocyte Lineages in Drosophila melanogaster Larvae after Wasp Infection

inferred← citeshttps://doi.org/10.1371/journal.ppat.1005961openalex-snapshot

The Drosophila CD36 Homologue croquemort Is Required to Maintain Immune and Gut Homeostasis during Development and Aging

inferred← citeshttps://doi.org/10.1371/journal.ppat.1006683openalex-snapshot

Parallel and costly changes to cellular immunity underlie the evolution of parasitoid resistance in three Drosophila species

inferred← citeshttps://doi.org/10.1371/journal.ppat.1007504openalex-snapshot

Immune-inducible non-coding RNA molecule lincRNA-IBIN connects immunity and metabolism in Drosophila melanogaster

inferred← citeshttps://doi.org/10.1371/journal.ppat.1008084openalex-snapshot

Independent effects on cellular and humoral immune responses underlie genotype-by-genotype interactions between Drosophila and parasitoids

inferred← citeshttps://doi.org/10.1371/journal.ppat.1008901openalex-snapshot

C-type lectin-mediated microbial homeostasis is critical for Helicoverpa armigera larval growth and development

inferred← citeshttps://doi.org/10.14232/phd.10133openalex-snapshot

A Headcase a Drosophila melanogaster vérsejtképződésének szabályozó faktora

inferred← citeshttps://doi.org/10.14232/phd.10682openalex-snapshot

Egy új vérsejt típus, a sokmagvú óriássejt szerepe a Drosophila sejt-közvetítette immunválaszában

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/10.14232/phd.2386openalex-snapshot

Vérsejtleszármazási vonalak vizsgálata Drosophila melanogasterben

inferred← citeshttps://doi.org/10.14232/phd.9954openalex-snapshot

A Candida parapsilosis in vivo fertőzés jellemzése: a sejtfal N-mannoziláció szerepe a virulenciában

inferred← citeshttps://doi.org/10.14348/molcells.2022.2039openalex-snapshot

Intrinsic and Extrinsic Regulation of Hematopoiesis in Drosophila

inferred← citeshttps://doi.org/10.14411/eje.2016.054openalex-snapshot

Cellular immune response of the Asian corn borer, Ostrinia furnacalis (Lepidoptera: Pyralidae), to infection by the entomopathogenic fungus, Beauveria bassiana

inferred← citeshttps://doi.org/10.15252/embj.2020104486openalex-snapshot

Temporal specificity and heterogeneity of Drosophila immune cells

inferred← citeshttps://doi.org/10.1534/g3.117.039487openalex-snapshot

The Immune Phenotype of ThreeDrosophilaLeukemia Models

inferred← citeshttps://doi.org/10.1534/g3.117.044172openalex-snapshot

A Genetic Screen Reveals an Unexpected Role for Yorkie Signaling in JAK/STAT-Dependent Hematopoietic Malignancies inDrosophila melanogaster

inferred← citeshttps://doi.org/10.1534/g3.119.400852openalex-snapshot

Maternal Priming of Offspring Immune System inDrosophila

inferred← citeshttps://doi.org/10.1534/genetics.113.159210openalex-snapshot

An Unexpected Link Between Notch Signaling and ROS in Restricting the Differentiation of Hematopoietic Progenitors in Drosophila

inferred← citeshttps://doi.org/10.1534/genetics.118.300223openalex-snapshot

Drosophila as a Genetic Model for Hematopoiesis

inferred← citeshttps://doi.org/10.15446/revfacmed.v63n1.44901openalex-snapshot

Comparison of hemocytes of 5th-instar nymphs of Rhodnius prolixus (Stal) and Rhodnius robustus (Larousse 1927), before and after molting

inferred← citeshttps://doi.org/10.1645/21-33openalex-snapshot

Review of the Role of Parasitic Nematode Excretory/Secretory Proteins in Host Immunomodulation

inferred← citeshttps://doi.org/10.17912/micropub.biology.000370openalex-snapshot

The S1A protease family members CG10764 and CG4793 regulate cellular immunity in Drosophila

inferred← citeshttps://doi.org/10.18632/oncotarget.10879openalex-snapshot

The human Smoothened inhibitor PF-04449913 induces exit from quiescence and loss of multipotentDrosophilahematopoietic progenitor cells

inferred← citeshttps://doi.org/10.21608/eajbsa.2023.312076openalex-snapshot

Immune Responses and Bioactive Peptides of Insect Hemolymph

inferred← citeshttps://doi.org/10.32607/actanaturae.27410openalex-snapshot

Molecular Mechanisms of Drosophila Hematopoiesis

inferred← citeshttps://doi.org/10.3389/fcell.2021.630272openalex-snapshot

Macrophages and Their Organ Locations Shape Each Other in Development and Homeostasis – A Drosophila Perspective

inferred← citeshttps://doi.org/10.3389/fimmu.2021.645359openalex-snapshot

Identification of Silkworm Hemocyte Subsets and Analysis of Their Response to Baculovirus Infection Based on Single-Cell RNA Sequencing

inferred← citeshttps://doi.org/10.3389/fimmu.2021.795331openalex-snapshot

Activin and BMP Signaling Activity Affects Different Aspects of Host Anti-Nematode Immunity in Drosophila melanogaster

inferred← citeshttps://doi.org/10.3389/fimmu.2022.1040510openalex-snapshot

Hemocytes and fat body cells, the only professional immune cell types in Drosophila, show strikingly different responses to systemic infections

inferred← citeshttps://doi.org/10.3389/fimmu.2022.856457openalex-snapshot

Advances in the Immune Regulatory Role of Non-Coding RNAs (miRNAs and lncRNAs) in Insect-Pathogen Interactions

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1122451openalex-snapshot

Parasitic nematode secreted phospholipase A2 suppresses cellular and humoral immunity by targeting hemocytes in Drosophila melanogaster

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1169152openalex-snapshot

Insect-pathogen crosstalk and the cellular-molecular mechanisms of insect immunity: uncovering the underlying signaling pathways and immune regulatory function of non-coding RNAs

inferred← citeshttps://doi.org/10.3389/fimmu.2023.1322381openalex-snapshot

Distinctive features of Zaprionus indianus hemocyte differentiation and function revealed by transcriptomic analysis

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/fmicb.2022.991678openalex-snapshot

Drosophila melanogaster as a model to study innate immune memory

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/10.3389/fphys.2019.00654openalex-snapshot

Ultrastructural and Cytotoxic Effects of Metarhizium robertsii Infection on Rhipicephalus microplus Hemocytes

inferred← citeshttps://doi.org/10.3390/cells12010024openalex-snapshot

A Novel Method for Primary Blood Cell Culturing and Selection in Drosophila melanogaster

inferred← citeshttps://doi.org/10.3390/genes10030173openalex-snapshot

Headcase is a Repressor of Lamellocyte Fate in Drosophila melanogaster

inferred← citeshttps://doi.org/10.3390/ijms23147767openalex-snapshot

Peeling Back the Layers of Lymph Gland Structure and Regulation

inferred← citeshttps://doi.org/10.3390/insects11010062openalex-snapshot

Drosophila melanogaster Responses against Entomopathogenic Nematodes: Focus on Hemolymph Clots

inferred← citeshttps://doi.org/10.3390/insects11020085openalex-snapshot

Thioester-Containing Proteins in the Drosophila melanogaster Immune Response against the Pathogen Photorhabdus

inferred← citeshttps://doi.org/10.3390/insects12050423openalex-snapshot

Morphological Characterisation of Haemocytes in the Mealworm Beetle Tenebrio molitor (Coleoptera, Tenebrionidae)

inferred← citeshttps://doi.org/10.3390/pathogens10010049openalex-snapshot

Immune Cell Production Is Targeted by Parasitoid Wasp Virulence in a Drosophila–Parasitoid Wasp Interaction

inferred← citeshttps://doi.org/10.3390/pathogens5030058openalex-snapshot

Parasitic Nematode Immunomodulatory Strategies: Recent Advances and Perspectives

inferred← citeshttps://doi.org/10.3844/ajassp.2020.204.213openalex-snapshot

Assessment of the Toxic Effects of Chitosan-Coated Magnetite Nanoparticles on Drosophila melanogaster

inferred← citeshttps://doi.org/10.47328/ufvbbt.2023.242openalex-snapshot

Caracterização dos hemócitos de subcastas de operárias da formiga-cortadeira Atta sexdens rubropilosa (Hymenoptera: formicidae)

inferred← citeshttps://doi.org/10.53501/rteufemud.1759958openalex-snapshot

Böceklerde Hemositlerin Morfolojik, Sitokimyasal Ve Fonksiyonel Özellikleri

inferred← citeshttps://doi.org/10.5772/67107openalex-snapshot

Cellular and Molecular Mechanisms of Insect Immunity

inferred← citeshttps://doi.org/10.5772/intechopen.96008openalex-snapshot

Molecular Dynamics of Mosquito-Plasmodium vivaxInteraction: A Smart Strategy of Parasitism

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709599openalex-snapshot

Additional file 1 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709602openalex-snapshot

Additional file 2 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709605openalex-snapshot

Additional file 3 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709608openalex-snapshot

Additional file 4 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709611openalex-snapshot

Additional file 5 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709614openalex-snapshot

Additional file 6 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709617openalex-snapshot

Additional file 7 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.6084/m9.figshare.26709620openalex-snapshot

Additional file 8 of Recognition of nonself is necessary to activate Drosophila’s immune response against an insect parasite

inferred← citeshttps://doi.org/10.64898/2026.01.09.698745openalex-snapshot

Single-cell RNA analysis reveals unexpected hemocyte plasticity and immune cell specialization in a Drosophila overgrowth model

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/10.70675/10ab0f8az3243z40b8z8d8ezdccd2af897afopenalex-snapshot

Deciphering the impact of perturbations in developmental hematopoiesis

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/10.70675/4f6c0817ze164z4cb2za1e9z261d78b0a7feopenalex-snapshot

Detection of microbial proteases by the Toll pathway during innate immune responses in Drosophila melanogaster

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/c5e08f8ezbe6az4ec5zad5fz5f4d91e38709openalex-snapshot

Étude comparative de la réactivité des cellules du système immunitaire (invertébrés et vertébrés) vis-à-vis des pesticides

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.06166openalex-snapshot

Drosophila sessile hemocyte clusters are true hematopoietic tissues that regulate larval blood cell differentiation

inferred← citeshttps://doi.org/10.7554/elife.19535openalex-snapshot

Symbiont-induced odorant binding proteins mediate insect host hematopoiesis

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.57297openalex-snapshot

Eater cooperates with Multiplexin to drive the formation of hematopoietic compartments

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