Document text
Principal Investigator: Julia Marie Perhacs
Organization: DREXEL UNIVERSITY
Fiscal Year: 2024
Award: $48,974
Funding agency: National Institute of Neurological Disorders and Stroke
Abstract
Neuronal function depends on the precise localization and release of neuromodulators, such as growth
factors, in response to stimuli. Our lab recently identified an unexpected, but exciting role for ER stress sensor
PERK, PKR-like ER kinase, in neuronal growth factor localization. Specifically, in the absence of PERK, a
dendritic TGF-ß-like growth factor is mistargeted to the axons, while an axonal insulin-like-growth factor (IGF) is
retained in the cell body. Interestingly, PERK is genetically linked to the tauopathies Alzheimer’s Disease (AD)
and Progressive Supranuclear Palsy (PSP). At least two of the three genetic variants have decreased kinase
activity, but it is unknown how decreased activity is a risk for disease. Impairment of PERK’s role in the correct
localization of neuroprotective IGF and TGF-ß-like growth factors could provide a molecular connection to
neurodegeneration.
Because it is unclear how PERK may directly mediate growth factor localization, I asked whether PERK
functions through one of its known downstream targets. Strikingly, I found that CaMKII, a kinase whose function
is critical for neural plasticity and memory, is genetically downstream of PERK. Importantly, CaMKII has a known
function in axonal targeting of neuropeptides, which has the potential to explain PERK’s novel role in growth
factor localization. This proposal aims to define how PERK and CaMKII interact to control axonal-dendritic
targeting of select neuroprotective growth factors. To do this, I will test whether PERK acts through its kinase
activity, whether phosphorylation-dependent activation state of CaMKII affects growth factor localization, and
whether PERK directly phosphorylates CaMKII. The proposed studies will be completed primarily at Drexel
University under the guidance of the sponsor and co-sponsor; however, I will seek guidance from my
collaborators at UPenn, especially for the advanced in vitro kinase assays to test whether PERK directly
phosphorylates CaMKII proposed in Aim 2. Together with my sponsors, I have developed a comprehensive
training plan that addresses training in hypothesis-driven research, scientific communication and writing, and
career development, as well as augmenting my formal training in neuroscience. The overarching goal of this pre-
doctoral fellowship project is to guide me in preparing for an independent career in biomedical research, focusing
on the areas related to protein-based pathology in neurodegeneration.
Terms: <AD dementia><Address><Affect><Alleles><Allelomorphs><Alzheimer Type Dementia><Alzheimer disease dementia><Alzheimer sclerosis><Alzheimer syndrome><Alzheimer's><Alzheimer's Disease><Alzheimers Dementia><Animals><Antibodies><Area><Assay><Axon><Bioassay><Biological><Biological Assay><Biomedical Research><Bone-Derived Transforming Growth Factor><C elegans><C. elegans><C.elegans><CNS plasticity><CaM KII><CaM PK II><CaM kinase II><CaMKII><Caenorhabditis elegans><Calcium><Cell Body><Cells><Communication><Data><Dendrites><Dependence><EIF-2 alpha><EIF-2alpha><EIF-2α><ER stress><Epistasis><Epistatic Deviation><Exhibits><Fellowship><Gene variant><Genetic><Genetic Alteration><Genetic Change><Genetic Epistasis><Genetic defect><Goals><Growth Agents><Growth Factor><Growth Substances><Impairment><In Vitro><Insulin-Like Growth Factors><Interaction Deviation><Kinases><Lab Findings><Laboratory Finding><Link><Mammalia><Mammals><Mass Photometry/Spectrum Analysis><Mass Spectrometry><Mass Spectroscopy><Mass Spectrum><Mass Spectrum Analyses><Mass Spectrum Analysis><Measures><Mediating><Memory><Mice><Mice Mammals><Milk Growth Factor><Modeling><Molecular><Murine><Mus><Mutation><Nerve Cells><Nerve Degeneration><Nerve Unit><Neural Cell><Neurites><Neurocyte><Neuromodulator><Neuron Degeneration><Neuronal Plasticity><Neurons><Neuropeptides><Neurosciences><PERK kinase><PRK-like ER kinase><Pathology><Pathway interactions><Phenocopy><Phenotype><Phosphorylation><Phosphorylation Site><Phosphotransferase Gene><Phosphotransferases><Platelet Transforming Growth Factor><Play><Post-Transcriptional Gene Silencing><Posttranscriptional Gene Silencing><Primary Senile Degenerative Dementia><Progressive Supranuclear Ophthalmoplegia><Progressive Supranuclear Palsy><Protein Phosphorylation><Proteins><Proteins Growth Factors><RNA Interference><RNA Silencing><RNAi><Research><Risk Factors><Role><Sequence-Specific Posttranscriptional Gene Silencing><Site><Somatomedins><Steele-Richardson-Olszewski Disease><Steele-Richardson-Olszewski Syndrome><Stimulus><Sulfation Factor><Synapses><Synaptic><TGF B><TGF-beta><TGF-β><TGFbeta><TGFβ><Tauopathies><Testing><Training><Transforming Growth Factor beta><Transforming Growth Factor-Beta Family Gene><Transphosphorylases><Universities><Writing><allele variant><allelic variant><alpha Subunit Eukaryotic Initiation Factor 2><biologic><calcium-dependent CaM kinase II><calmodulin-dependent protein kinase II><career><career development><central nervous system plasticity><disease risk><disorder risk><endoplasmic reticulum stress><epistatic relationship><gain of function><gene x gene interaction><genetic epistases><genetic variant><genome mutation><genomic variant><insight><insulinlike growth factor><loss of function><mimetics><mutant><neural degeneration><neural plasticity><neurodegeneration><neurodegenerative><neurological degeneration><neuron development><neuronal><neuronal degeneration><neuronal development><neuronal growth><neuropathologic tau><neuropathological tau><neuroplastic><neuroplasticity><neuroprotection><neuroprotective><novel><pathway><perk gene product><pre-doc><pre-doctoral><predoctoral><primary degenerative dementia><response><senile dementia of the Alzheimer type><sensor><social role><synapse><tau associated neurodegeneration><tau associated neurodegenerative process><tau induced neurodegeneration><tau mediated neurodegeneration><tau neurodegenerative disease><tau neuropathology><tauopathic neurodegenerative disorder><tauopathy><trafficking>