Cerebrospinal fluid soluble insulin receptor levels in Alzheimer's disease

Author:

Thomas Peter1,Leclerc Manon23,Evitts Kira45,Brown Caitlin1,Miller Wyatt1,Hanson Angela J.6,Banks William A.16,Gibbons Laura7,Domoto‐Reilly Kimiko8,Jayadev Suman8,Li Ge1910,Peskind Elaine910,Young Jessica E.511, ,Calon Frederic23,Rhea Elizabeth M.16

Affiliation:

1. Geriatric Research Education and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA

2. Faculty of Pharmacy Laval University Quebec Quebec Canada

3. Neuroscience Axis CHU de Québec Research Center − Laval University Quebec Quebec Canada

4. Department of Bioengineering University of Washington Seattle Washington USA

5. Institute for Stem Cells and Regenerative Medicine University of Washington Seattle Washington USA

6. Department of Medicine, Division of Gerontology and Geriatric Medicine University of Washington School of Medicine Seattle Washington USA

7. Department of Medicine University of Washington Seattle Washington USA

8. Department of Neurology University of Washington Seattle Washington USA

9. Veterans Affairs Northwest Mental Illness Research, Education, and Clinical Center Veterans Affairs Puget Sound Health Care System Seattle Washington USA

10. Department of Psychiatry and Behavioral Sciences University of Washington School of Medicine Seattle Washington USA

11. Department of Laboratory Medicine and Pathology University of Washington School of Medicine Seattle Washington USA

Abstract

AbstractINTRODUCTIONBrain insulin resistance and deficiency is a consistent feature of Alzheimer's disease (AD). Insulin resistance can be mediated by the surface expression of the insulin receptor (IR). Cleavage of the IR generates the soluble IR (sIR).METHODSWe measured the levels of sIR present in cerebrospinal fluid (CSF) from individuals along the AD diagnostic spectrum from two cohorts: Seattle (n = 58) and the Consortium for the Early Identification of Alzheimer's Disease‐Quebec (CIMA‐Q; n = 61). We further investigated the brain cellular contribution for sIR using human cell lines.RESULTSCSF sIR levels were not statistically different in AD. CSF sIR and amyloid beta (Aβ)42 and Aβ40 levels significantly correlated as well as CSF sIR and cognition in the CIMA‐Q cohort. Human neurons expressing the amyloid precursor protein “Swedish” mutation generated significantly greater sIR and human astrocytes were also able to release sIR in response to both an inflammatory and insulin stimulus.DISCUSSIONThese data support further investigation into the generation and role of sIR in AD.Highlights Cerebrospinal fluid (CSF) soluble insulin receptor (sIR) levels positively correlate with amyloid beta (Aβ)42 and Aβ40. CSF sIR levels negatively correlate with cognitive performance (Montreal Cognitive Assessment score). CSF sIR levels in humans remain similar across Alzheimer's disease diagnostic groups. Neurons derived from humans with the “Swedish” mutation in which Aβ42 is increased generate increased levels of sIR. Human astrocytes can also produce sIR and generation is stimulated by tumor necrosis factor α and insulin.

Publisher

Wiley

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