4.2 Article

G1/S Cell Cycle Checkpoint Defect in Lymphocytes from Patients with Alzheimer's Disease

Journal

PSYCHIATRY INVESTIGATION
Volume 9, Issue 4, Pages 413-417

Publisher

KOREAN NEUROPSYCHIATRIC ASSOC
DOI: 10.4306/pi.2012.9.4.413

Keywords

Alzheimer's disease; Cell cycle; Biomarker

Categories

Funding

  1. National Research Foundation of Korea
  2. Korean government (MEST) [R0A 2007-000-20129-0]
  3. Korea Health 21 RD Project
  4. Ministry of Health & Welfare, Republic of Korea [A030001]
  5. National Research Foundation of Korea [R0A-2007-000-20129-0] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Objective We compared the cell responsiveness of activated lymphocytes to rapamycin, which blocks the G1/S transition, between patients with Alzheimer's disease (AD) and normal controls to assess the early phase control defect in cell cycle. Methods Blood samples of 26 patients with AD and 28 normal controls were collected to separate peripheral lymphocytes. We measured the proportion of each cell cycle phase in activated lymphocytes using flow cytometry and evaluated the responsiveness of these lymphocytes to rapamycin. Results The patients with AD were older than the normal controls (AD 74.03 +/- 7.90 yr vs. control 68.28 +/- 6.21 yr, p=0.004). The proportion of G1 phase cells in the AD group was significantly lower than that in the control group (70.29 +/- 6.32% vs. 76.03 +/- 9.05%, p=0.01), and the proportion of S phase cells in the AD group was higher than that in control group (12.45 +/- 6.09% vs. 6.03 +/- 5.11%, p=0.001). Activated lymphocytes in patients with AD were not arrested in the G1 phase and they progressed to the late phase of the cell cycle despite rapamycin treatment, in contrast to those of normal subjects. Conclusion The patients with AD probably have a control defect of early phase cell cycle in peripheral lymphocytes that may be associated with the underlying pathology of neuronal death. Psychiatry Investig 2012;9:413-417

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