The goals of Core D (Neuropathology) are to perform postmortem neuropathologic evaluations of participants in the Udall Center. In addition, Core D will provide neuropathologic support to research projects, in particular tau biochemical support and immunohistochemistry for Project 2 , as well as tissue processing and histology for Project 3. Core D will also assist Project 3 with electron microscopic studies. To accomplish these objectives, the specific aims of Core D will:
Specific Aim 1. Perform standardized diagnostic neuropathologic evaluations and data collection on all brains harvested locally or sent to the Udall Center by referring physicians, with particular focus on cases followed by Core B. This will include a) immunostaining of cortical, hippocampal and basal forebrain sections for a-synuclein to record density of Lewy bodies in multiple cortical regions;b) characterizing non-Lewy body Parkinsonian degenerative disorders with immunocytochemistry, including antibodies to tau, TDP-43, ubiquitin, FUS, a-internexin and aB-crystallin, recording estimates of neuronal and glial lesions in neocortex, hippocampus, basal ganglia, thalamus, subthalamic nucleus, midbrain, pons, medulla and cerebellar dentate nucleus for cases with tauopathy;c) assessing Alzheimer type pathology with counts of senile plaques and neurofibrillary tangles in multiple cortical and subcortical areas with thioflavin-S fluorescent microscopy, and assign a Braak neurofibrillary tangle stage on all cases;and d) using validated neuropathologic research criteria for those disorders for which such criteria have been established and """"""""best clinical practice"""""""" for uncommon disorders for which research criteria do not yet exist.
Specific Aim 2. Provide frozen human brain samples or DNA to investigators in the Udall Center, particulady Projects 1 and 2, as well as to qualified investigators at other research institutions.
Specific Aim 3. Assist Projects 2 with biochemical studies of tau protein in human brain samples.
Specific Aim 4. Assist Project 3 with neuropathologic characterization of mouse models subjected to drug treatments and with electron microscopic support to evaluate effects of drugs on tau and a-synuclein fibrillization.

Public Health Relevance

The """"""""gold standard"""""""" for diagnosis of neurodegenerative disorders, such as Parkinson disease (PD), is neuropathology, which is the medical specialty that uses microscopic evaluation of tissue changes to arrive at a diagnosis. Accurate diagnosis is critical to finding genes and other factors that cause PD, which are the first steps in the process of finding a cure for PD and related disorders.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS072187-05
Application #
8724258
Study Section
Special Emphasis Panel (ZNS1-SRB-J)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
5
Fiscal Year
2014
Total Cost
$158,978
Indirect Cost
$57,395
Name
Mayo Clinic Jacksonville
Department
Type
DUNS #
153223151
City
Jacksonville
State
FL
Country
United States
Zip Code
32224
Jiang, Peizhou; Dickson, Dennis W (2018) Parkinson's disease: experimental models and reality. Acta Neuropathol 135:13-32
Tsai, Pei-I; Lin, Chin-Hsien; Hsieh, Chung-Han et al. (2018) PINK1 Phosphorylates MIC60/Mitofilin to Control Structural Plasticity of Mitochondrial Crista Junctions. Mol Cell 69:744-756.e6
Deutschländer, A B; Ross, O A; Dickson, D W et al. (2018) Atypical parkinsonian syndromes: a general neurologist's perspective. Eur J Neurol 25:41-58
Konno, T; Miura, T; Harriott, A M et al. (2018) Partial loss of function of colony-stimulating factor 1 receptor in a patient with white matter abnormalities. Eur J Neurol 25:875-881
Ferman, Tanis J; Aoki, Naoya; Crook, Julia E et al. (2018) The limbic and neocortical contribution of ?-synuclein, tau, and amyloid ? to disease duration in dementia with Lewy bodies. Alzheimers Dement 14:330-339
Koga, S; Lin, W-L; Walton, R L et al. (2018) TDP-43 pathology in multiple system atrophy: colocalization of TDP-43 and ?-synuclein in glial cytoplasmic inclusions. Neuropathol Appl Neurobiol 44:707-721
Deutschländer, Angela B; Boeve, Bradley F; Rosen, Howard J et al. (2018) Tau Mutations as a Novel Risk Factor for Cancer-Letter. Cancer Res 78:6523-6524
Zhao, Na; Liu, Chia-Chen; Van Ingelgom, Alexandra J et al. (2018) APOE ?2 is associated with increased tau pathology in primary tauopathy. Nat Commun 9:4388
Koga, Shunsuke; Dickson, Dennis W (2018) ""Minimal change"" multiple system atrophy with limbic-predominant ?-synuclein pathology. Acta Neuropathol :
Koga, Shunsuke; Kouri, Naomi; Walton, Ronald L et al. (2018) Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype. Acta Neuropathol :

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