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Brain Amyloid-Beta Fragment Signatures in Pathological Ageing and Alzheimer's Disease by Hybrid Immunoprecipitation Mass Spectrometry

Portelius, Erik, 1977 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Lashley, T. (author)
Westerlund, Anna, 1981 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
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Persson, Rita, 1951 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Fox, N. C. (author)
Blennow, Kaj, 1958 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
Revesz, T. (author)
Zetterberg, Henrik, 1973 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi,Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry
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 (creator_code:org_t)
2015-01-13
2015
English.
In: Neurodegenerative Diseases. - : S. Karger AG. - 1660-2854 .- 1660-2862. ; 15:1, s. 50-57
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: Senile plaques in Alzheimer's disease (AD) are composed of amyloid-beta (A beta) especially N-truncated forms including A beta(4-42). These are thought to be neurotoxic. However, individuals may live for decades with biomarker evidence of cerebral beta-amyloidosis (positive amyloid PET imaging and/or low cerebrospinal fluid levels of the 42 amino acid form of A beta) without cognitive impairment. This condition may be termed pathological ageing (PA). Objective: To investigate whether there is a difference in the cerebral A beta fragment pattern in brain specimens from non-demented (PA) and demented (AD) individuals expressing the full neuropathological triad of AD (senile plaques, neurofibrillary tangles and neurodegeneration). Methods: We extracted A beta using formic acid and hybrid (6E10 and 4G8) immunoprecipitation from fresh-frozen temporal cortex tissue of 6 elderly individuals (mean age +/- SD:89 +/- 3.5 years) with PA and 10 patients with AD (mean age +/- SD: 72 +/- 8.5 years). The full spectrum of A beta peptides was determined by matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Results: AD patients had generally more N-terminally truncated and pyroglutamate-modified A beta than PA patients, whereas PA patients had on average more A beta(1-40) than AD patients. Conclusion: Senile plaques in AD may have an AB fragment composition distinct from PA with more N-terminally and pyroglutamate-modified A beta peptides that may be linked to neurotoxicity. (C) 2015 S. Karger AG, Basel

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Neurologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Neurology (hsv//eng)

Keyword

Alzheimer's disease
Pathological ageing
Amyloid precursor protein
Amyloid-beta
Brain
CEREBROSPINAL-FLUID
BIOMARKER CHANGES
PEPTIDES
PROTEIN
DEMENTIA
CASCADE
ONSET
Clinical Neurology

Publication and Content Type

ref (subject category)
art (subject category)

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