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

• Published in: Frontiers in neuroscience 2018-07, Vol.12, p.476-476
• Main Authors: Bonham, Luke W, Geier, Ethan G, Steele, Natasha Z R, Holland, Dominic, Miller, Bruce L, Dale, Anders M, Desikan, Rahul S, Yokoyama, Jennifer S
• Format: Article
• Language: English
• Subjects: Alzheimer's disease; Animal models; Astrocytes; Atrophy; Biomarkers; Cerebrospinal fluid; Cognitive ability; CSF; Dementia; Diabetes; Disease resistance; Gene expression; Hippocampus; IGFBP-2; Insulin; Insulin resistance; Insulin-like growth factor-binding protein 2; Insulin-like growth factors; Medical imaging; Memory; Neurodegeneration; Neurodegenerative diseases; Neuroimaging; Neurons; Neuroscience; Pathogenesis; Pathology; Plasma; Proteins; Studies; tau; Tau protein; Transgenic mice
• ISSN: 1662-4548; 1662-453X; 1662-453X
• DOI: 10.3389/fnins.2018.00476

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 in tau pathobiology, we evaluated the expression of 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 in both transgenic mouse models relative to wild-type mice in cortex but not in hippocampus. In both humans and mice, 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.