Journal
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY
Volume 34, Issue 2, Pages 181-+Publisher
BLACKWELL PUBLISHING
DOI: 10.1111/j.1365-2990.2007.00885.x
Keywords
Alzheimer's disease; angiotensin-converting enzyme; angiotensin-converting enzyme-1; cerebral amyloid angiopathy; decorin; fibronectin
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Funding
- Alzheimers Research UK [ART-EG2005B-1] Funding Source: researchfish
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Aims: Several observations point to the involvement of angiotensin-converting enzyme-1 (ACE-1) in Alzheimer's disease (AD): ACE-1 cleaves amyloid-beta peptide (A beta) in vitro, the level and activity of ACE-1 are reportedly increased in AD, and variations in the ACE-1 gene are associated with AD. We analysed ACE-1 activity and expression in AD and control brains, particularly in relation to A beta load and cerebral amyloid angiopathy (CAA). Methods: ACE-1 activity was measured in the frontal cortex from 58 control and 114 AD cases of known A beta load and CAA severity. The distribution of ACE-1 was examined immunohistochemically. In five AD cases with absent or mild CAA, five with moderate to severe CAA and five controls with absent or mild CAA, levels of vascular ACE-1 were assessed by quantitative immunofluorescence. Results: ACE-1 activity was increased in AD (P < 0.001) and correlated directly with parenchymal A beta load (P = 0.05). Immunohistochemistry revealed ACE-1 in neurones and cortical blood vessels - in the intima but most abundant perivascularly. Cases with moderate to severe CAA had significantly more vessel-associated ACE-1 than did those with little or no CAA. Perivascular ACE-1 did not colocalize with A beta, smooth muscle actin, glial fibrillary acidic protein, collagen IV, vimentin or laminin, but was similarly distributed to extracellular matrix (ECM) proteins fibronectin and decorin. Conclusions: Our findings indicate that ACE-1 activity is increased in AD, in direct relationship to parenchymal A beta load. Increased ACE-1, probably of neuronal origin, accumulates perivascularly in severe CAA and colocalizes with vascular ECM. The possible relationship of ACE-1 to the deposition of perivascular ECM remains to be determined.
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