grant

The Development of Facial Motor Neuron Subtypes in Health and in Congenital Facial Weakness

Organization BOSTON CHILDREN'S HOSPITALLocation BOSTON, UNITED STATESPosted 25 Sept 2020Deadline 30 Nov 2026
NIHUS FederalResearch GrantFY20252-photon21+ years oldAcuteAddressAdultAdult HumanAmericanBehavioralBiologyBrainBrain Nervous SystemC1 qC1qCause of DeathCell BodyCellsCessation of lifeChronicChronic PhaseClinicalCommunicable DiseasesComplementComplement 1qComplement C1qComplement ProteinsComplexDeathDeveloping fetusDevelopmentDiseaseDisorderDrugsEEGElectroencephalogramElectroencephalographyEncephalonEnsureEnvironmentExcitatory SynapseFaceFacultyFetal DevelopmentGeneticGliaGlial CellsGoalsGroups at riskHealthHistoryHortega cellHumanHuman FigureHuman bodyImageImmune responseImmunocompromisedImmunocompromised HostImmunocompromised PatientImmunosuppressed HostIndividualInfectionInfectious DiseasesInfectious Diseases / LaboratoryInfectious Diseases ResearchInfectious DisorderInflammationInflammatory ResponseInfrastructureInhibitory SynapseInnate Immune SystemInstitutionInterdisciplinary ResearchInterdisciplinary StudyKnowledgeKolliker's reticulumLabelLifeLong-term infectionMacrophageMediatingMedicationMental disordersMental health disordersMentorsMiceMice MammalsMicrogliaMissionModern ManMolecularMotor CellMotor NeuronsMultidisciplinary CollaborationMultidisciplinary ResearchMurineMusNational Institutes of HealthNerveNerve CellsNerve Impulse TransmissionNerve TransmissionNerve UnitNervous System DiseasesNervous System DisorderNeural CellNeurocyteNeurogliaNeuroglial CellsNeuroimmuneNeuroimmune MechanismsNeuroimmune ProcessesNeuroimmunomodulationNeurologicNeurologic DisordersNeurologicalNeurological DisordersNeuronal InjuryNeuronal TransmissionNeuronsNeurosciencesNon-neuronal cellNonneuronal cellOrganParasitesParasitic infectionPathogenesisPathway interactionsPeople at riskPersons at riskPhagocytosisPharmaceutical PreparationsPhasePopulationPopulations at RiskPostdocPostdoctoral FellowPredispositionPrevalenceProteinsPsychiatric DiseasePsychiatric DisorderPublishingR-Series Research ProjectsR01 MechanismR01 ProgramRecording of previous eventsRecordsReportingResearchResearch AssociateResearch GrantsResearch Project GrantsResearch ProjectsResidenciesRetinaRiskRisk FactorsRoleSchizophreniaSchizophrenic DisordersSeizuresSkeletal MuscleSurfaceSusceptibilitySynapsesSynapticT gondiiT gondii infectionT. gondiiT. gondii infectionTestingTherapeuticTimeToxoplasma gondiiToxoplasma gondii InfectionToxoplasmosisTrainingTransgenic OrganismsTranslatingTropismUnited StatesUnited States National Institutes of HealthUniversitiesVoluntary MuscleWorkadulthoodaxon signalingaxon-glial signalingaxonal signalingbrain circuitrychronic infectioncomplement pathwaycomplementationdementia praecoxdevelopmentaldrug/agentexperimentexperimental researchexperimental studyexperimentsfacesfacialfood-born illnessfood-borne diseasefood-borne illnessfoodborn illnessfoodborne diseasefoodborne illnessgitter cellglia signalingglial activationglial cell activationglial signalinghistorieshost responseimage-based methodimagingimaging methodimaging modalityimmune system responseimmunoneurologyimmunoresponseimmunosuppressed patientinfected with parasitesinsightinterdisciplinary collaborationmental illnessmesogliamicroglial cellmicrogliocytemolecular arraymotoneuronnerve cementnerve signalingneuralneural circuitneural circuitryneural signalingneurocircuitryneuroimmunologyneurological diseaseneuron injuryneuronalneuronal signalingneurotransmissionnew drug treatmentsnew drugsnew pharmacological therapeuticnew therapeuticsnew therapynext generation therapeuticsnovelnovel drug treatmentsnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel therapeuticsnovel therapyparasite infectionparasite invasionpathogenpathwayperivascular glial cellpersistent infectionpost-docpost-doctoralpost-doctoral traineepre-clinicalpreclinicalpresynapticpreventpreventingprogramspsychiatric illnesspsychological disorderresearch associatesresponseschizophrenicsocial rolesuccesssynapsesynaptic circuitsynaptic circuitrytenure processtenure tracktooltransdisciplinary collaborationtransgenictwo-photon
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Full Description

PROJECT SUMMARY
Aberrant changes in mature neural connections and their function can be induced by infection and inflammation

within the brain. The intracellular protozoan parasite, Toxoplasma gondii, is one pathogen that infects the brain,

evokes a prolonged inflammatory response and can cause seizures. Persistent infection by this parasite is also

associated with behavioral alterations and is a considerable risk factor for developing psychiatric illness, includ-

ing schizophrenia. Over 30% of Americans are presently living with an incurable long-term infection of Toxo-

plasma gondii, yet, despite its prevalence and implications for serious neurological disorders, we lack sufficient

understanding of the effect of life-long parasitic infection on the brain – a major organ of the human body in which

the parasite invades cells. This study seeks to elucidate the underlying mechanisms of brain circuitry dysregu-

lation in long-term infection in response to this unmet need. Our recent studies have revealed that Toxoplasma

gondii brain infection causes changes in inhibitory circuitry (specifically the loss of inhibitory synapses) along

with changes in inhibitory neurotransmission, leading to the onset of seizures. Moreover, preliminary studies

demonstrating increased expression of classical complement cascade components, elevated microglial activa-

tion, and substantial microglial ensheathment of neurons and inhibitory nerve terminals, propose dynamic inter-

active roles for the innate immune system and resident-macrophages of the brain in altering functionally mature

neural circuits during parasitic infection. In this proposal, we test the hypotheses that molecular components of

the innate complement pathway mediate inhibitory synapse loss and seizures, and that microglia remove and

phagocytose these synapses following chronic Toxoplasma gondii infection. By capitalizing on multi-scale imag-

ing modalities, the aims in this proposal will deliver novel ultrastructural and real-time insight into the impact of

chronic parasitic infection on mature neural circuits and will offer a novel mechanism as to how persistent Toxo-

plasma gondii infection may contribute to both seizures and psychiatric illness. This study is directly aligned with

the NIH's Blueprint Program's mission to expand our understanding of the neuroimmune dynamic interactions

that give way to neurological disorders.

Grant Number: 5K00NS120596-05
NIH Institute/Center: NIH

Principal Investigator: Gabriela Carrillo

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