Source:http://linkedlifedata.com/resource/pubmed/id/11561167
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
|
pubmed:dateCreated |
2001-9-18
|
pubmed:abstractText |
The scope of this review is to discuss the new advances in our understanding of the role of scavenger receptor class A in the initiation and modulation of the atherosclerotic process. Through the approaches of gene manipulation in the mouse model, a substantial body of literature has accumulated that depicts scavenger receptor class A as a central player in atherogenesis. In studies of scavenger receptor class A overexpression in macrophages through bone marrow transplantation using transgenic donor material, recipient mice with hyperlipidemia caused either by apolipoprotein E or LDL receptor deficiency did not show convincing changes in the degree of atherosclerosis development compared with controls. Conversely, the deletion of the scavenger receptor class A gene in the mouse has shown, in a consistent and significant fashion, that this receptor serves a pro-atherogenic function under hyperlipidemic conditions, as both apolipoprotein E and LDL receptor-deficient mice had reduced atherosclerosis in the absence of scavenger receptor class A. In addition, we have recently shown that C57BL/6 mice are protected from diet-induced atherosclerosis when they lack scavenger receptor class A, and that the macrophage is the cell type responsible for the effect of scavenger receptor class A deficiency in reducing lesion formation in C57BL/6 and LDL receptor null mice. Together, these results demonstrate that macrophage scavenger receptor class A contributes significantly to atherosclerotic lesion formation, and suggest that the uptake of oxidized or modified lipoproteins by vessel wall macrophages is a central process in atherogenesis.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD36,
http://linkedlifedata.com/resource/pubmed/chemical/MSR1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Msr1 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Immunologic,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Scavenger,
http://linkedlifedata.com/resource/pubmed/chemical/Scavenger Receptors, Class A
|
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0957-9672
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
12
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
489-95
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:11561167-Animals,
pubmed-meshheading:11561167-Antigens, CD36,
pubmed-meshheading:11561167-Arteriosclerosis,
pubmed-meshheading:11561167-Disease Models, Animal,
pubmed-meshheading:11561167-Foam Cells,
pubmed-meshheading:11561167-Gene Deletion,
pubmed-meshheading:11561167-Humans,
pubmed-meshheading:11561167-Hyperlipidemias,
pubmed-meshheading:11561167-Macrophages,
pubmed-meshheading:11561167-Mice,
pubmed-meshheading:11561167-Mice, Inbred C57BL,
pubmed-meshheading:11561167-Receptors, Immunologic,
pubmed-meshheading:11561167-Receptors, LDL,
pubmed-meshheading:11561167-Receptors, Scavenger,
pubmed-meshheading:11561167-Scavenger Receptors, Class A
|
pubmed:year |
2001
|
pubmed:articleTitle |
Class A scavenger receptors, macrophages, and atherosclerosis.
|
pubmed:affiliation |
Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA. macrae.linton@mcmail.vanderbilt.edu
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Review,
Research Support, Non-U.S. Gov't
|