Astrocyte-neuron interactions in the developing auditory system
Astrocyte-neuron interactions in the developing auditory system
批准号:
9792244
负责人:
Vered Kellner
金额:
$3.28万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-30 至 2020-03-29
关键词:
AblationAction PotentialsAffectAgeAnimalsAstrocytesAuditoryAuditory areaAuditory systemBehaviorBrainCalciumCalcium SignalingCochleaDevelopmentDiseaseExcitatory Amino Acid AntagonistsExhibitsFire - disastersFrequenciesGlutamate ReceptorGlutamatesHearingImageImpairmentIn Situ HybridizationInferior ColliculusInjuryKnockout MiceLesionMapsMeasuresMediatingMetabotropic Glutamate ReceptorsMethodsMolecularMusNeuronsPathway interactionsPatternPeriodicityPharmacologyQuantitative Reverse Transcriptase PCRReceptor SignalingReverse Transcriptase Polymerase Chain ReactionRoleSensorySensory ProcessShapesSignal TransductionStereotypingStimulusSynapsesTestingTimeTransgenic MiceViralVirusauditory pathwayawakecalcium indicatorcritical developmental periodcritical perioddevelopmental diseasein vivoin vivo imaginginsightmRNA Expressionneuronal circuitryneuronal patterningpostsynapticpresynapticreceptorreceptor expressionrelating to nervous systemrelease factorresponsesensory systemsound
中文摘要
项目总结
英文摘要
Project Summary
Spontaneous neuronal activity that occurs in the auditory pathway prior to hearing onset is characterized by
highly stereotyped, periodic bursts of action potentials that originate in the cochlea and propagate through
auditory centers of the brain. Neuronal activity in the developing inferior colliculus (IC) occurs in discrete
bands, corresponding to tonotopic frequency maps that are apparent after hearing onset. In preliminary
studies, I found that astrocytes in the IC show periodic, tonotopically organized elevations of intracellular
calcium before hearing onset that are strikingly similar to the activity patterns exhibited by IC neurons at this
age. This study aims to define the molecular mechanisms underlying this signaling in astrocytes and assess
whether this dynamic interaction between astrocytes and neurons promotes neuronal circuit maturation.
The studies will test the hypothesis that periodic elevation of intracellular calcium in astrocytes is dependent on
activation of astrocyte metabotropic glutamate receptors (mGluR5) by glutamate released from ascending
projections into the developing IC. In the first aim I will image neuronal and astrocyte calcium activity
simultaneously in transgenic mice that express genetically encoded calcium indicators to define the spatial and
temporal interactions between neurons and astrocytes in the developing IC. I will selectively manipulate
neuronal activity and measure the effect on astrocytic calcium signaling.
In the second aim I will determine whether the correlated activity of astrocytes is mediated by mGluR5
receptors. First I will define the mRNA expression levels and spatial localization of mGluR5 using qRT-PCR
and in situ hybridization during different developmental time points. Next, I will use pharmacological
manipulations and astrocyte specific conditional knockout mice to inhibit mGluR5 receptors in vivo while
imaging calcium activity in astrocytes.
In the third aim, I will investigate whether manipulation of this early pattern of astrocyte activity affects the
firing behavior of IC neurons prior to hearing onset and the tonotopic representation of sound in hearing
animals. I will use transgenic mouse lines that impair astrocyte calcium activity and measure the
consequences on the spatial pattern of neuronal activity in the IC, induced spontaneously or in response to
stereotyped sound stimuli. To define specifically the role of astrocytes in the IC, I will manipulate astrocyte
calcium locally using viruses and measure the effect on the functional refinement of neuronal circuits.
This analysis of reciprocal interactions between neurons and astrocytes in the developing auditory system
will provide new insight into the mechanisms that induce neuronal circuit refinement to enable hearing. These
studies may reveal new pathways to promote circuit maturation and identify new targets for treatment of
developmental disorders by expanding our understanding of how alterations in astrocytes during this critical
period of development impact the ability of auditory circuits to process sensory information.
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