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https://ahro.austin.org.au/austinjspui/handle/1/10573
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wookey, Peter J | - |
dc.contributor.author | Zulli, Anthony | - |
dc.contributor.author | Buxton, Brian F | - |
dc.contributor.author | Hare, David L | - |
dc.date.accessioned | 2015-05-16T00:04:33Z | |
dc.date.available | 2015-05-16T00:04:33Z | |
dc.date.issued | 2008-04-01 | en |
dc.identifier.citation | Histopathology; 52(5): 605-12 | en |
dc.identifier.govdoc | 18370957 | en |
dc.identifier.other | PUBMED | en |
dc.identifier.uri | https://ahro.austin.org.au/austinjspui/handle/1/10573 | en |
dc.description.abstract | To determine and quantify calcitonin receptor (CTR) immunoreactivity associated with specific cell types within, and associated with, the endothelial layers, neo-intima, media and vasa vasorum of diseased radial and internal mammary arteries.Immunohistochemistry and anti-CTR antibodies were used to identify positive cells within remnants of diseased human radial (n = 3) and internal mammary arteries (n = 4) that remained after bypass surgery. Three cell types expressed CTR, including endothelial cells, fibroblast-like cells within the neo-intima, and cellular structures aligned with the smooth muscle cells of the media. Other smaller cells within the surrounding parenchyma of the vasa vasorum of diseased vessels and blood-borne cells were also immunoreactive. Immunoquantification of CTR expression (Intensity x Proportional Area) in the endothelium (P < 0.05), neo-intima (P < 0.02) and media (P < 0.03) established a significant statistical correlation (Students' two-tailed t-test) with the ratio of intimal/media thickness.Increased immunoreactivity developed using anti-CTR antibodies was associated with specific cell types in the endothelial layers, neo-intima, media and vasa vasorum of diseased regions of radial and internal mammary arteries, in which there was an increased intimal/media ratio. Furthermore, CTR+, blood-borne cells present in the vessels of diseased regions suggest recruitment into these surrounding tissues. | en |
dc.language.iso | en | en |
dc.subject.other | Aged | en |
dc.subject.other | Biological Markers.metabolism | en |
dc.subject.other | Calcinosis.metabolism.pathology | en |
dc.subject.other | Endothelium, Vascular.metabolism.pathology | en |
dc.subject.other | Fluorescent Antibody Technique, Indirect | en |
dc.subject.other | Humans | en |
dc.subject.other | Male | en |
dc.subject.other | Mammary Arteries.metabolism.pathology | en |
dc.subject.other | Middle Aged | en |
dc.subject.other | Radial Artery.metabolism.pathology | en |
dc.subject.other | Receptors, Calcitonin.metabolism | en |
dc.subject.other | Tunica Media.metabolism.pathology | en |
dc.title | Calcitonin receptor immunoreactivity associated with specific cell types in diseased radial and internal mammary arteries. | en |
dc.type | Journal Article | en |
dc.identifier.journaltitle | Histopathology | en |
dc.identifier.affiliation | Departments of Cardiology, Medicine (University of Melbourne), and Cardiac Surgery, Austin Health, Heidelberg, Victoria, Australia | en |
dc.identifier.doi | 10.1111/j.1365-2559.2008.02979.x | en |
dc.description.pages | 605-12 | en |
dc.identifier.orcid | 0000-0001-9554-6556 | - |
dc.identifier.pubmedid | 18370957 | - |
dc.type.austin | Journal Article | en |
local.name.researcher | Buxton, Brian F | |
item.languageiso639-1 | en | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.fulltext | No Fulltext | - |
crisitem.author.dept | Medicine (University of Melbourne) | - |
crisitem.author.dept | Cardiac Surgery | - |
crisitem.author.dept | Cardiology | - |
Appears in Collections: | Journal articles |
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