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Publication . Article . 2018

Insulin-Like Growth Factor Binding Protein 2 Is Associated With Biomarkers of Alzheimer's Disease Pathology and Shows Differential Expression in Transgenic Mice

Luke W. Bonham; Luke W. Bonham; Ethan G. Geier; Natasha Z. R. Steele; Dominic Holland; Bruce L. Miller; Anders M. Dale; +5 Authors
Open Access
English
Published: 01 Jul 2018
Publisher: eScholarship, University of California
Country: United States
Abstract
There is increasing evidence that metabolic dysfunction plays an important role in Alzheimer’s disease (AD). Brain insulin resistance and subsequent impairment of insulin and insulin-like growth factor (IGF) signaling are associated with the neurodegenerative and clinical features of AD. Nevertheless, how the brain insulin/IGF signaling system is altered in AD and the effects of these changes on AD pathobiology are not well understood. IGF binding protein 2 (IGFBP-2) is an abundant cerebral IGF signaling protein and there is early evidence suggesting it associates with AD biomarkers. We evaluated the relationship between protein levels of IGFBP-2 with cerebrospinal fluid (CSF) biomarkers and neuroimaging markers of AD progression in 300 individuals from across the AD spectrum. CSF IGFBP-2 levels were correlated with CSF tau levels and brain atrophy in non-hippocampal regions. To further explore the role of IGFBP2 in tau pathobiology, we evaluated the expression of IGFBP2 in different human and mouse brain cell types and brain tissue from two transgenic mouse models: the P301L-tau model of tauopathy and TASTPM model of AD. We observed significant differential expression of IGFBP2 in both transgenic mouse models relative to wild-type mice in cortex but not in hippocampus. In both humans and mice, IGFBP2 is most highly expressed in astrocytes. Taken together, our findings suggest that IGFBP-2 may be linked to tau pathology and provides further evidence for a relationship between metabolic dysregulation and neurodegeneration. Our results also raise the possibility that this relationship may extend beyond neurons.
Subjects by Vocabulary

Microsoft Academic Graph classification: Hippocampus Insulin medicine.medical_treatment medicine Genetically modified mouse Tauopathy medicine.disease Internal medicine medicine.medical_specialty Cerebrospinal fluid Insulin-like growth factor-binding protein biology.protein biology Endocrinology Insulin resistance Neurodegeneration

Library of Congress Subject Headings: lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry lcsh:RC321-571

Subjects

IGFBP-2, Alzheimer's disease, CSF, neuroimaging, tau, Alzheimer’s Disease Neuroimaging Initiative, Alzheimer’s disease, Acquired Cognitive Impairment, Neurodegenerative, Brain Disorders, Alzheimer's Disease including Alzheimer's Disease Related Dementias, Aging, Dementia, Neurosciences, 2.1 Biological and endogenous factors, Neurological, Cognitive Sciences, Psychology, Neuroscience, Original Research, IGFBP-2, Alzheimer’s disease, CSF, neuroimaging, tau, General Neuroscience, Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD), Aetiology

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NIH| RNA signatures of frontotemporal dementia and ALS due to C9ORF72 expansion
Project
  • Funder: National Institutes of Health (NIH)
  • Project Code: 5K01AG049152-03
  • Funding stream: NATIONAL INSTITUTE ON AGING
,
NIH| DATA MANAGEMENT AND BIOSTATISTICS
Project
  • Funder: National Institutes of Health (NIH)
  • Project Code: 5P50AG023501-03
  • Funding stream: NATIONAL INSTITUTE ON AGING
,
NIH| Alzheimers Disease Neuroimaging Initiative
Project
  • Funder: National Institutes of Health (NIH)
  • Project Code: 1U01AG024904-01
  • Funding stream: NATIONAL INSTITUTE ON AGING
,
CIHR
Project
  • Funder: Canadian Institutes of Health Research (CIHR)
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