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Acta Neuropathologica

, Volume 123, Issue 1, pp 39–52 | Cite as

Apolipoprotein E level and cholesterol are associated with reduced synaptic amyloid beta in Alzheimer’s disease and apoE TR mouse cortex

  • Stephen Arold
  • Patrick Sullivan
  • Tina Bilousova
  • Edmond Teng
  • Carol A. Miller
  • Wayne W. Poon
  • Harry V. Vinters
  • Lindsey B. Cornwell
  • Tommy Saing
  • Gregory M. Cole
  • Karen Hoppens GylysEmail author
Original Paper

Abstract

The apolipoprotein E4 allele (APOE4) contributes to Alzheimer’s disease (AD) risk and APOE2 is protective, but the relevant cellular mechanisms are unknown. We have used flow cytometry analysis to measure apolipoprotein E (apoE) and amyloid beta peptide (Aβ) levels in large populations of synaptic terminals from AD and aged cognitively normal controls, and demonstrate that modest but significant increases in soluble apoE levels accompany elevated Aβ in AD cortical synapses and in an APP/PS1 rat model of AD. Dual labeling experiments document co-localization of apoE and Aβ in individual synapses with concentration of Aβ in a small population of apoE-positive synapses in both AD and controls. Consistent with a clearance role, the apoE level was higher in Aβ-positive synapses in control cases. In aged targeted replacement mice expressing human apoE, apoE2/4 synaptic terminals demonstrated the highest level of apoE and the lowest level of Aβ compared to apoE3/3 and apoE4/4 lines. In apoE2/4 terminals, the pattern of immunolabeling for apoE and Aβ closely resembled the pattern in human control cases, and elevated apoE was accompanied by elevated free cholesterol in apoE2/4 synaptic terminals. These results are consistent with a role for APOE in Aβ clearance in AD synapses, and suggest that optimal lipidation of apoE2 compared to E3 and E4 makes an important contribution to Aβ clearance and synaptic function.

Keywords

Synaptosome Flow cytometry Filipin Ganglioside GM1 Triple transgenic mouse Triple transgenic rat 

Notes

Acknowledgments

This work was supported by NIH AG27465 to KHG, by NIH NS43946 to GMC, by NIA AG18879 to CAM. HVV is supported by the Daljit S. and Elaine Sarkaria Chair in Diagnostic Medicine. Tissue was obtained from the the Alzheimer’s Disease Research Center Neuropathology Cores of USC (NIA 050 AG05142), UCLA (NIA P50 AG 16970), and UC Irvine (NIA P50 AG016573). Flow cytometry was performed in the UCLA Jonsson Comprehensive Cancer Center (JCCC) and Center for AIDS Research Flow Cytometry Core Facility supported by NIH CA16042 and AI 28697, and by the JCCC, the UCLA AIDS Institute, the David Geffen School of Medicine and the Chancellor’s Office at UCLA. ET is supported by K08 AG-34628 (jointly sponsored by NIA, AFAR, the John A. Hartford Foundation and the Atlantic Philanthropies, the Starr Foundation, and an anonymous donor).

Supplementary material

401_2011_892_MOESM1_ESM.doc (58 kb)
Supplementary material 1 (DOC 58 kb)
401_2011_892_MOESM2_ESM.doc (282 kb)
Supplementary material 2 (DOC 281 kb)

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Copyright information

© Springer-Verlag 2011

Authors and Affiliations

  • Stephen Arold
    • 1
  • Patrick Sullivan
    • 2
  • Tina Bilousova
    • 1
  • Edmond Teng
    • 3
    • 6
  • Carol A. Miller
    • 7
  • Wayne W. Poon
    • 8
  • Harry V. Vinters
    • 3
    • 5
  • Lindsey B. Cornwell
    • 8
  • Tommy Saing
    • 8
  • Gregory M. Cole
    • 3
    • 4
    • 6
  • Karen Hoppens Gylys
    • 1
    Email author
  1. 1.School of Nursing and Mary S. Easton Center for Alzheimer’s ResearchUCLALos AngelesUSA
  2. 2.Department of MedicineDuke University Medical CenterDurhamUSA
  3. 3.Department of NeurologyUCLA School of MedicineLos AngelesUSA
  4. 4.Department of MedicineUCLA School of MedicineLos AngelesUSA
  5. 5.Department of Pathology and Laboratory MedicineUCLA School of MedicineLos AngelesUSA
  6. 6.Sepulveda VAMC GRECCLos AngelesUSA
  7. 7.Departments of Pathology, Neurology, and Program in NeuroscienceKeck USC School of MedicineLos AngelesUSA
  8. 8.Institute for Memory Impairments and Neurological DisordersUC IrvineIrvineUSA

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