Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
10
|
pubmed:dateCreated |
1998-11-2
|
pubmed:abstractText |
The acyl coenzyme A:cholesterol acyltransferase (ACAT) gene was first cloned in 1993 (Chang et al, J Biol Chem. 1993;268:20747-20755; designated ACAT-1). Using affinity-purified antibodies raised against the N-terminal portion of human ACAT-1 protein, we performed immunohistochemical localization studies and showed that the ACAT-1 protein was highly expressed in atherosclerotic lesions of the human aorta. We also performed cell-specific localization studies using double immunostaining and showed that ACAT-1 was predominantly expressed in macrophages but not in smooth muscle cells. We then used a cell culture system in vitro to monitor the ACAT-1 expression in differentiating monocytes-macrophages. The ACAT-1 protein content increased by up to 10-fold when monocytes spontaneously differentiated into macrophages. This increase occurred within the first 2 days of culturing the monocytes and reached a plateau level within 4 days of culturing, indicating that the increase in ACAT-1 protein content is an early event during the monocyte differentiation process. The ACAT-1 protein expressed in the differentiating monocytes-macrophages was shown to be active by enzyme assay in vitro. The high levels of ACAT-1 present in macrophages maintained in culture can explain the high ACAT-1 contents found in atherosclerotic lesions. Our results thus support the idea that ACAT-1 plays an important role in differentiating monocytes and in forming macrophage foam cells during the development of human atherosclerosis.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
1079-5642
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
18
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1568-74
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:9763528-Adult,
pubmed-meshheading:9763528-Aged,
pubmed-meshheading:9763528-Animals,
pubmed-meshheading:9763528-Arteriosclerosis,
pubmed-meshheading:9763528-Cells, Cultured,
pubmed-meshheading:9763528-Female,
pubmed-meshheading:9763528-Humans,
pubmed-meshheading:9763528-Macrophages,
pubmed-meshheading:9763528-Male,
pubmed-meshheading:9763528-Middle Aged,
pubmed-meshheading:9763528-Monocytes,
pubmed-meshheading:9763528-Rabbits,
pubmed-meshheading:9763528-Sterol O-Acyltransferase
|
pubmed:year |
1998
|
pubmed:articleTitle |
Expression of ACAT-1 protein in human atherosclerotic lesions and cultured human monocytes-macrophages.
|
pubmed:affiliation |
Department of Biochemistry, Dartmouth Medical School, Hanover, NH, USA, the Second Department of Pathology and the Department of Biochemistry Kumamoto University School of Medicine, Kumamo, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|