Publication: Distinctive peri-luminal presence of agrin in murine and human carotid atherosclerotic plaques
Authors
Rauch, Uwe ; Bengtsson, Eva ; Gonçalves, Isabel ; Hultgårdh Nilsson, Anna
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Publisher
Universidad de Murcia. Departamento de Biología Celular e Histología
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DOI
DOI: 10.14670/HH-11-970
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info:eu-repo/semantics/article
Description
Abstract
The clinical consequences of arterial
atherosclerotic lesions depend, apart from their size, on
their composition of cellular and extracellular
components. While an intact endothelium at the interface
of atherosclerotic plaques towards the blood can prevent
its erosion, underlying smooth muscle cells within the
plaque can reduce the risk of plaque ruptures, due to the
deposition of stabilizing extracellular matrix. Basement
membranes underlay and support the function of
endothelial cells, and embed smooth muscle cells in the
media, the source of most smooth muscle cells within
atherosclerotic plaques.
In the present study mouse atherosclerotic plaques
were comparatively analyzed for the basement
membrane components laminin, type IV collagen,
perlecan, and agrin. Distinct agrin immunofluorescence
was found in the peri-luminal area in mouse carotid
atherosclerotic plaques. Agrin was also clearly present in
the media, with a significant increase in regions directly
associated with plaque tissue.
In addition, ten human endarterectomy specimens
were investigated for this heparan sulfate proteoglycan.
No statistically significant differences in agrin
immunofluorescence were noticed between five
specimens from symptomatic and five from
asymptomatic patients. In all these plaques agrin was
present in a distinctive manner in a narrow zone partially
or almost completely surrounding the lumen.
Additionally it was also present around the small lumina
of the CD31-positive neovessels. The presence of agrin
at locations with particular importance for the growth
and stability of atherosclerotic plaques renders this
molecule strategically positioned to influence plaque
development and vulnerability.
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Citation
Histology and Histopathology, Vol.33, nº7, (2018)
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