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Morphofunctional programming of microglia requires distinct roles of type II myosins
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1 of the 99 references listed on this page is in the Retraction Watch database as retracted (export 2026-11-04): 10.1038/nn.3560 (notice 2022-01-13).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1098-1136(200103)33:3<256::aid-glia1024>3.0.co;2-jopenalex-snapshot
Dynamics of microglial activation: A confocal time-lapse analysis in hippocampal slices
inferredcites →https://doi.org/10.1002/glia.21266openalex-snapshot
Identification of a microglia phenotype supportive of remyelination
inferredcites →https://doi.org/10.1002/jnr.23036openalex-snapshot
Myosin II is a negative regulator of oligodendrocyte morphological differentiation
inferredcites →https://doi.org/10.1006/bbrc.2001.5388openalex-snapshot
Iba1 Is an Actin-Cross-Linking Protein in Macrophages/Microglia
inferredcites →https://doi.org/10.1007/978-1-61779-170-3_4openalex-snapshot
Microglia Cell Culture: A Primer for the Novice
inferredcites →https://doi.org/10.1007/s10974-004-6060-7openalex-snapshot
Specificity of blebbistatin, an inhibitor of myosin II
inferredcites →https://doi.org/10.1016/j.cell.2013.11.030openalex-snapshot
Microglia Promote Learning-Dependent Synapse Formation through Brain-Derived Neurotrophic Factor
inferredcites →https://doi.org/10.1016/j.cellsig.2003.10.001openalex-snapshot
Phosphorylation of profilin regulates its interaction with actin and poly (?proline)
inferredcites →https://doi.org/10.1016/j.celrep.2018.04.087openalex-snapshot
Myosin IIa Promotes Antibody Responses by Regulating B Cell Activation, Acquisition of Antigen, and Proliferation
inferredcites →https://doi.org/10.1016/j.celrep.2019.05.010openalex-snapshot
Nanoscale Surveillance of the Brain by Microglia via cAMP-Regulated Filopodia
inferredcites →https://doi.org/10.1016/j.celrep.2020.107537openalex-snapshot
Knocking Out Non-muscle Myosin II in Retinal Ganglion Cells Promotes Long-Distance Optic Nerve Regeneration
inferredcites →https://doi.org/10.1016/j.celrep.2020.107796openalex-snapshot
Microglia Dysfunction Caused by the Loss of Rhoa Disrupts Neuronal Physiology and Leads to Neurodegeneration
inferredcites →https://doi.org/10.1016/j.cub.2010.07.004openalex-snapshot
Cytoskeletal Cross-linking and Bundling in Motor-Independent Contraction
inferredcites →https://doi.org/10.1016/j.cub.2011.03.039openalex-snapshot
A Novel Spatiotemporal RhoC Activation Pathway Locally Regulates Cofilin Activity at Invadopodia
inferredcites →https://doi.org/10.1016/j.cub.2014.03.059openalex-snapshot
Stresses at the Cell Surface during Animal Cell Morphogenesis
inferredcites →https://doi.org/10.1016/j.cub.2019.09.040openalex-snapshot
RhoA Controls Axon Extension Independent of Specification in the Developing Brain
inferredcites →https://doi.org/10.1016/j.devcel.2012.04.015openalex-snapshot
Actin Depolymerization Drives Actomyosin Ring Contraction during Budding Yeast Cytokinesis
inferredcites →https://doi.org/10.1016/j.devcel.2015.05.013openalex-snapshot
Actin Filament Turnover Drives Leading Edge Growth during Myelin Sheath Formation in the Central Nervous System
inferredcites →https://doi.org/10.1016/j.devcel.2015.06.011openalex-snapshot
CNS Myelin Wrapping Is Driven by Actin Disassembly
inferredcites →https://doi.org/10.1016/j.immuni.2016.02.024openalex-snapshot
Tissue-Resident Macrophage Ontogeny and Homeostasis
inferredcites →https://doi.org/10.1016/j.neuron.2012.03.026openalex-snapshot
Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner
inferredcites →https://doi.org/10.1016/j.neuron.2017.12.002openalex-snapshot
Microglial Ramification, Surveillance, and Interleukin-1β Release Are Regulated by the Two-Pore Domain K+ Channel THIK-1
inferredcites →https://doi.org/10.1016/j.neuron.2019.07.007openalex-snapshot
ADF/Cofilin-Mediated Actin Turnover Promotes Axon Regeneration in the Adult CNS
inferredcites →https://doi.org/10.1016/j.stem.2010.08.014openalex-snapshot
Microglia Shape Adult Hippocampal Neurogenesis through Apoptosis-Coupled Phagocytosis
inferredcites →https://doi.org/10.1016/j.tcb.2004.07.003openalex-snapshot
The role of profilin complexes in cell motility and other cellular processes
inferredcites →https://doi.org/10.1016/j.tcb.2006.11.009openalex-snapshot
Cell type-specific functions of Rho GTPases revealed by gene targeting in mice
inferredcites →https://doi.org/10.1016/j.tcb.2012.07.001openalex-snapshot
Actin cortex mechanics and cellular morphogenesis
inferredcites →https://doi.org/10.1016/j.tibs.2018.06.006openalex-snapshot
Targeting Myosin by Blebbistatin Derivatives: Optimization and Pharmacological Potential
inferredcites →https://doi.org/10.1016/j.xpro.2020.100147openalex-snapshot
A Protocol for FRET-Based Live-Cell Imaging in Microglia
inferredcites →https://doi.org/10.1016/j.yexcr.2010.04.011openalex-snapshot
Protrusion and actin assembly are coupled to the organization of lamellar contractile structures
inferredcites →https://doi.org/10.1038/31729openalex-snapshot
Regulation of actin dynamics through phosphorylation of cofilin by LIM-kinase
inferredcites →https://doi.org/10.1038/ncb2072openalex-snapshot
Myosin II isoforms identify distinct functional modules that support integrity of the epithelial zonula adherens
inferredcites →https://doi.org/10.1038/ncb2205openalex-snapshot
A role for actin arcs in the leading-edge advance of migrating cells
inferredcites →https://doi.org/10.1038/ncb3387openalex-snapshot
Mechanical regulation of transcription controls Polycomb-mediated gene silencing during lineage commitment
inferredcites →https://doi.org/10.1038/ncb3525openalex-snapshot
Actin cortex architecture regulates cell surface tension
inferredcites →https://doi.org/10.1038/ni.1636openalex-snapshot
The NALP3 inflammasome is involved in the innate immune response to amyloid-β
inferredcites →https://doi.org/10.1038/ni.1723openalex-snapshot
T cell antigen receptor signaling and immunological synapse stability require myosin IIA
inferredcites →https://doi.org/10.1038/nn.3531openalex-snapshot
A new type of microglia gene targeting shows TAK1 to be pivotal in CNS autoimmune inflammation
inferredcites →https://doi.org/10.1038/nn.3560openalex-snapshot
RETRACTED ARTICLE: TGF-β signaling regulates neuronal C1q expression and developmental synaptic refinement
inferredcites →https://doi.org/10.1038/nn1472openalex-snapshot
ATP mediates rapid microglial response to local brain injury in vivo
inferredcites →https://doi.org/10.1038/nn1805openalex-snapshot
The P2Y12 receptor regulates microglial activation by extracellular nucleotides
inferredcites →https://doi.org/10.1038/nn1997openalex-snapshot
Microglia: active sensor and versatile effector cells in the normal and pathologic brain
inferredcites →https://doi.org/10.1038/nprot.2006.37openalex-snapshot
Production and purification of lentiviral vectors
inferredcites →https://doi.org/10.1038/nprot.2013.143openalex-snapshot
Genome engineering using the CRISPR-Cas9 system
inferredcites →https://doi.org/10.1038/nri.2017.125openalex-snapshot
Microglia and macrophages in brain homeostasis and disease
inferredcites →https://doi.org/10.1038/nri3244openalex-snapshot
Information processing during phagocytosis
inferredcites →https://doi.org/10.1038/nrm2786openalex-snapshot
Non-muscle myosin II takes centre stage in cell adhesion and migration
inferredcites →https://doi.org/10.1038/nsmb908openalex-snapshot
The structural basis of blebbistatin inhibition and specificity for myosin II
inferredcites →https://doi.org/10.1038/s41467-018-03566-5openalex-snapshot
Microglia remodel synapses by presynaptic trogocytosis and spine head filopodia induction
inferredcites →https://doi.org/10.1046/j.1365-2443.1996.05005.xopenalex-snapshot
Phosphorylation of Ser‐3 of cofilin regulates its essential function on actin
inferredcites →https://doi.org/10.1073/pnas.1116268109openalex-snapshot
Nonmuscle myosin II exerts tension but does not translocate actin in vertebrate cytokinesis
inferredcites →https://doi.org/10.1073/pnas.1525528113openalex-snapshot
New tools for studying microglia in the mouse and human CNS
inferredcites →https://doi.org/10.1073/pnas.94.23.12407openalex-snapshot
Nonmuscle myosin II-B is required for normal development of the mouse heart
inferredcites →https://doi.org/10.1074/jbc.c400352200openalex-snapshot
Defects in Cell Adhesion and the Visceral Endoderm following Ablation of Nonmuscle Myosin Heavy Chain II-A in Mice
inferredcites →https://doi.org/10.1074/jbc.m113.499848openalex-snapshot
Characterization of Three Full-length Human Nonmuscle Myosin II Paralogs
inferredcites →https://doi.org/10.1074/jbc.m305453200openalex-snapshot
Functional Divergence of Human Cytoplasmic Myosin II
inferredcites →https://doi.org/10.1074/jbc.r113.515486openalex-snapshot
Cell Type-specific Signaling Function of RhoA GTPase: Lessons from Mouse Gene Targeting
inferredcites →https://doi.org/10.1083/jcb.117.2.357openalex-snapshot
Astrocyte process growth induction by actin breakdown
inferredcites →https://doi.org/10.1083/jcb.200610005openalex-snapshot
Cofilin promotes stimulus-induced lamellipodium formation by generating an abundant supply of actin monomers
inferredcites →https://doi.org/10.1083/jcb.201208030openalex-snapshot
Immobile myosin-II plays a scaffolding role during cytokinesis in budding yeast
inferredcites →https://doi.org/10.1083/jcb.201612126openalex-snapshot
Concerted actions of distinct nonmuscle myosin II isoforms drive intracellular membrane remodeling in live animals
inferredcites →https://doi.org/10.1084/jem.20172244openalex-snapshot
Neuronal integrity and complement control synaptic material clearance by microglia after CNS injury
inferredcites →https://doi.org/10.1091/mbc.12.4.1131openalex-snapshot
Cofilin Phosphorylation by Protein Kinase Testicular Protein Kinase 1 and Its Role in Integrin-mediated Actin Reorganization and Focal Adhesion Formation
inferredcites →https://doi.org/10.1091/mbc.e03-03-0187openalex-snapshot
Myosin IIA Drives Neurite Retraction
inferredcites →https://doi.org/10.1091/mbc.e05-11-1001openalex-snapshot
PAK1 and aPKCζ Regulate Myosin II-B Phosphorylation: A Novel Signaling Pathway Regulating Filament Assembly
inferredcites →https://doi.org/10.1091/mbc.e09-10-0859openalex-snapshot
RhoA is dispensable for skin development, but crucial for contraction and directed migration of keratinocytes
inferredcites →https://doi.org/10.1091/mbc.e16-06-0461openalex-snapshot
A minimal actomyosin-based model predicts the dynamics of filopodia on neuronal dendrites
inferredcites →https://doi.org/10.1091/mbc.e18-12-0790openalex-snapshot
Nonmuscle myosin IIA and IIB differentially modulate migration and alter gene expression in primary mouse tumorigenic cells
inferredcites →https://doi.org/10.1093/nar/gkw398openalex-snapshot
CHOPCHOP v2: a web tool for the next generation of CRISPR genome engineering
inferredcites →https://doi.org/10.1098/rstb.2013.0005openalex-snapshot
Actin polymerization or myosin contraction: two ways to build up cortical tension for symmetry breaking
inferredcites →https://doi.org/10.1101/cshperspect.a018267openalex-snapshot
The Actin Cytoskeleton and Actin-Based Motility
inferredcites →https://doi.org/10.1126/science.1094561openalex-snapshot
Cofilin Promotes Actin Polymerization and Defines the Direction of Cell Motility
inferredcites →https://doi.org/10.1126/science.1110647openalex-snapshot
Resting Microglial Cells Are Highly Dynamic Surveillants of Brain Parenchyma in Vivo
inferredcites →https://doi.org/10.1126/science.1175862openalex-snapshot
Actin, a Central Player in Cell Shape and Movement
inferredcites →https://doi.org/10.1126/science.285.5429.895openalex-snapshot
Signaling from Rho to the Actin Cytoskeleton Through Protein Kinases ROCK and LIM-kinase
inferredcites →https://doi.org/10.1126/science.aat0474openalex-snapshot
Microglia and early brain development: An intimate journey
inferredcites →https://doi.org/10.1126/sciimmunol.abb1817openalex-snapshot
T cell engagement of cross-presenting microglia protects the brain from a nasal virus infection
inferredcites →https://doi.org/10.1128/mcb.00079-08openalex-snapshot
Phosphorylation of Profilin by ROCK1 Regulates Polyglutamine Aggregation
inferredcites →https://doi.org/10.1146/annurev-physiol-022516-034406openalex-snapshot
Microglia in Physiology and Disease
inferredcites →https://doi.org/10.1146/annurev-vision-091517-034425openalex-snapshot
Microglia in the Retina: Roles in Development, Maturity, and Disease
inferredcites →https://doi.org/10.1158/0008-5472.can-05-4236openalex-snapshot
Distinct Roles of Nonmuscle Myosin II Isoforms in the Regulation of MDA-MB-231 Breast Cancer Cell Spreading and Migration
inferredcites →https://doi.org/10.1161/01.res.0000089256.00309.cbopenalex-snapshot
Ablation and Mutation of Nonmuscle Myosin Heavy Chain II-B Results in a Defect in Cardiac Myocyte Cytokinesis
inferredcites →https://doi.org/10.1242/dev.02439openalex-snapshot
Coordinated cell-shape changes control epithelial movement in zebrafish and Drosophila
inferredcites →https://doi.org/10.1242/jcs.03084openalex-snapshot
RhoA-kinase coordinates F-actin organization and myosin II activity during semaphorin-3A-induced axon retraction
inferredcites →https://doi.org/10.1242/jcs.071928openalex-snapshot
Visualizing dynamic cytoplasmic forces with a compliance-matched FRET sensor
inferredcites →https://doi.org/10.1242/jcs.114.15.2713openalex-snapshot
Rho GTPases and cell migration
inferredcites →https://doi.org/10.1242/jcs.123547openalex-snapshot
Spatial regulation of RhoC activity defines protrusion formation in migrating cells
inferredcites →https://doi.org/10.1242/jcs.219899openalex-snapshot
Myosin-II activity generates a dynamic steady state with continuous actin turnover in a minimal actin cortex
inferredcites →https://doi.org/10.1242/jcs.232264openalex-snapshot
Pushing myelination – developmental regulation of myosin expression drives oligodendrocyte morphological differentiation
inferredcites →https://doi.org/10.1523/jneurosci.1854-18.2018openalex-snapshot
Complement Targets Newborn Retinal Ganglion Cells for Phagocytic Elimination by Microglia
inferredcites →https://doi.org/10.1523/jneurosci.4807-10.2011openalex-snapshot
The Small GTPase RhoA Is Required to Maintain Spinal Cord Neuroepithelium Organization and the Neural Stem Cell Pool
inferredcites →https://doi.org/10.15252/emmm.201505298openalex-snapshot
Microglial phagocytosis of living photoreceptors contributes to inherited retinal degeneration
inferredcites →https://doi.org/10.3389/fnmol.2015.00012openalex-snapshot
Intracellular calcium dynamics in cortical microglia responding to focal laser injury in the PC::G5-tdT reporter mouse
inferredcites →https://doi.org/10.3389/fnmol.2020.599948openalex-snapshot
Adult Mouse Retina Explants: From ex vivo to in vivo Model of Central Nervous System Injuries
inferredcites →https://doi.org/10.3791/52118openalex-snapshot
Generation of Genomic Deletions in Mammalian Cell Lines via CRISPR/Cas9
inferredcites →https://doi.org/10.7490/f1000research.1117828.1openalex-snapshot
FRET ratiometric tool: imageJ script
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/10.1016/bs.mcb.2022.08.003openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ejcb.2022.151247openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.pneurobio.2024.102586openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.5c00230openalex-snapshot
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inferred← citeshttps://doi.org/10.1038/s41419-023-06217-wopenalex-snapshot
RhoA balances microglial reactivity and survival during neuroinflammation
inferred← citeshttps://doi.org/10.1101/2024.09.27.615114openalex-snapshot
Deficiency of actin depolymerizing factors ADF/Cfl1 in microglia decreases motility and impairs memory
inferred← citeshttps://doi.org/10.1101/cshperspect.a041640openalex-snapshot
Innate Immunity and Parkinson's Disease
inferred← citeshttps://doi.org/10.1186/s44477-025-00012-xopenalex-snapshot
Differential downstream signaling in microglia lacking Alzheimer’s-related TREM2 or its adaptor TYROBP/DAP12
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