grant

Advancing simultaneous fMRI-multiphoton imaging technique to study brain function and connectivity across different scales at ultrahigh field

Organization UNIVERSITY OF MINNESOTALocation MINNEAPOLIS, UNITED STATESPosted 30 Sept 2020Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY20242-photon microscopyAblationAddressAffectAnesthesiaAnesthesia proceduresAnimal ModelAnimal Models and Related StudiesAnimalsAstrocytesAstrocytusAstrogliaBlood VesselsBrainBrain DiseasesBrain DisordersBrain Nervous SystemCell BodyCell Communication and SignalingCell SignalingCellsComplexConnector NeuronConsciousConsciousnessCorrelation StudiesDataDedicationsDiseaseDisorderDysfunctionEncephalonEncephalon DiseasesFunctional MRIFunctional Magnetic Resonance ImagingFunctional disorderGenerationsGoalsHealthHumanImageImaging ProceduresImaging TechnicsImaging TechniquesImaging technologyImplanted ElectrodesIndividualInstitutionIntercalary NeuronIntercalated NeuronsInterneuronsInternuncial CellInternuncial NeuronIntracellular Communication and SignalingIntracranial CNS DisordersIntracranial Central Nervous System DisordersKnowledgeLaser ElectromagneticLaser RadiationLasersMR ImagingMR TomographyMRIMRIsMagnetic Resonance ImagingMapsMeasurementMeasuresMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMetabolicMethodsMiceMice MammalsMicroscopicModalityModern ManMurineMusNMR ImagingNMR TomographyNerveNerve CellsNerve Impulse TransmissionNerve TransmissionNerve UnitNervous SystemNeural CellNeurocyteNeurologic Body SystemNeurologic Organ SystemNeuronal TransmissionNeuronsNeurosciencesNeurosciences ResearchNuclear Magnetic Resonance ImagingOutcomePhysiopathologyPopulationPositionPositioning AttributeProcessRecordsResearchResolutionRestRoleSignal TransductionSignal Transduction SystemsSignalingSpecificityStatistical CorrelationSystemTechniquesTechnologyTimeWorkZeugmatographyastrocytic gliaawakeaxon signalingaxon-glial signalingaxonal signalingbiological signal transductionblood oxygen level dependentblood oxygenation level dependentbrain researchdesigndesigningfMRIglia signalingglial signalinghemodynamicsimagingimaging systeminhibitory neuroninnovateinnovationinnovativeinsightmagnetic fieldmicroscope imagingmicroscopic imagingmicroscopy imagingmodel of animalmulti-modal neuro-imagingmulti-modal neuroimagingmulti-photon imagingmultimodal neuro-imagingmultimodal neuroimagingmultiphoton excitation microscopymultiphoton imagingmultiphoton microscopynerve signalingneuralneural circuitneural circuitryneural imagingneural networkneural signalingneuro-imagingneuro-vascularneurocircuitryneuroimagingneurological imagingneuronalneuronal signalingneurophysiologicalneurophysiologyneurotransmissionneurovascularnew technologynext generationnovelnovel technologiesoptic imagingoptical imagingpathophysiologypre-clinicalpreclinicalresolutionsresponsesocial rolespatiotemporalsuccesssuper high resolutionsuperresolutionsynaptic circuitsynaptic circuitrytooltwo photon excitation microscopytwo photon microscopyultra high resolutionvascular
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Full Description

PROJECT SUMMARY
Understanding the neural circuitry and signaling in health or diseased brain requires new tools that can image

neuronal activity and functional connectivity with superior spatiotemporal precision across various scales from

individual and population of neural cells and microvessel at microscopic scale, neural circuits and cortical

layers/columns, and functional connectivity at mesoscopic (or laminar) scale to neural networks at macroscopic

scale and the nervous system level. Functional magnetic resonance imaging (fMRI) based on the blood-

oxygenation-level-dependent (BOLD) contrast has gained a prominent position in neuroscience, and it is the

only neuroimaging modality that can noninvasively map human neuronal activity and dynamic change to the

level of neural computational units, and image functional connectivity and resting-state networks (RSNs)

covering the entire brain. However, the fMRI BOLD signal is determined by a complex interplay between vascular

and metabolic changes, thus, indirectly reflecting neuronal activity. The inference of underlying neuronal activity

on the fMRI BOLD signal can be affected by many unknown factors at microscopic and mesoscopic scales.

Although great efforts have been made to study the correlation between fMRI signals and neuronal activity, the

neurophysiology origin of the BOLD signal and its specificity in mapping neuronal activity and functional

connectivity at cortical lamina level remains elusive.

To tackle technical challenges and address critical neuroimaging and neuroscience questions, we have

formed an interdisciplinary team with experts in the ultrahigh-field (UHF) fMRI and multi-photon microscopy

imaging research fields from two research institutions to develop the world first MRI fully compatible volumetric

two-photon microscopy imaging (VTPMI) system, which works in one of the highest field animal MRI scanners

at 16.4T Tesla. This novel VTPMI-fMRI multimodal neuroimaging system will make it possible to simultaneously

measure key neurophysiological information related to activities and dynamics of excitatory/inhibitory neurons,

astrocytes, different sized vessels, and ultrahigh-resolution fMRI data, thus enables delineation of cell- and layer-

specific neuronal activity in the living brain. The VTPMI-fMRI technology developed in this project will be

employed to study the neuro-vascular correlation and the specificity of resting-state fMRI BOLD signals for

mapping the layer-specific functional connectivity in anesthetized and awake brains, with particular emphasis on

investigating the roles of inhibitory interneurons. The findings and knowledge from this project will be

transformative and beneficial for understanding and interpreting the human fMRI BOLD signals at the fine scale

of fundamental computational units.

Grant Number: 5R01NS118330-05
NIH Institute/Center: NIH

Principal Investigator: Wei Chen

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