Source:http://linkedlifedata.com/resource/pubmed/id/16985254
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2007-2-6
|
pubmed:abstractText |
Steroid hormones are synthesized using cholesterol as precursor. To determine the functional importance of the low density lipoprotein (LDL) receptor and hormone-sensitive lipase (HSL) in adrenal steroidogenesis, adrenal cells were isolated from control, HSL(-/-), LDLR(-/-), and double LDLR/HSL(-/-) mice. The endocytic and selective uptake of apolipoprotein E-free human high density lipoprotein (HDL)-derived cholesteryl esters did not differ among the mice, with selective uptake accounting for >97% of uptake. In contrast, endocytic uptake of either human LDL- or rat HDL-derived cholesteryl esters was reduced 80-85% in LDLR(-/-) and double-LDLR/HSL(-/-) mice. There were no differences in the selective uptake of either human LDL- or rat HDL-derived cholesteryl esters among the mice. Maximum corticosterone production induced by ACTH or dibutyryl cyclic AMP and lipoproteins was not altered in LDLR(-/-) mice but was reduced 80-90% in HSL(-/-) mice. Maximum corticosterone production was identical in HSL(-/-) and double-LDLR/HSL(-/-) mice. These findings suggest that, although the LDL receptor is responsible for endocytic delivery of cholesteryl esters from LDL and rat HDL to mouse adrenal cells, it appears to play a negligible role in the delivery of cholesterol for acute adrenal steroidogenesis in the mouse. In contrast, HSL occupies a vital role in adrenal steroidogenesis because of its link to utilization of selectively delivered cholesteryl esters from lipoproteins.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cholesterol Esters,
http://linkedlifedata.com/resource/pubmed/chemical/Corticosterone,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, LDL,
http://linkedlifedata.com/resource/pubmed/chemical/Steroids,
http://linkedlifedata.com/resource/pubmed/chemical/Sterol Esterase
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0193-1849
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
292
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
E408-12
|
pubmed:dateRevised |
2007-11-15
|
pubmed:meshHeading |
pubmed-meshheading:16985254-Adrenal Cortex,
pubmed-meshheading:16985254-Animals,
pubmed-meshheading:16985254-Cells, Cultured,
pubmed-meshheading:16985254-Cholesterol Esters,
pubmed-meshheading:16985254-Corticosterone,
pubmed-meshheading:16985254-Humans,
pubmed-meshheading:16985254-Mice,
pubmed-meshheading:16985254-Mice, Inbred C57BL,
pubmed-meshheading:16985254-Mice, Knockout,
pubmed-meshheading:16985254-Rats,
pubmed-meshheading:16985254-Receptors, LDL,
pubmed-meshheading:16985254-Steroids,
pubmed-meshheading:16985254-Sterol Esterase
|
pubmed:year |
2007
|
pubmed:articleTitle |
The LDL receptor is not necessary for acute adrenal steroidogenesis in mouse adrenocortical cells.
|
pubmed:affiliation |
Veterans Affairs Palo Alto Health Care System, Palo Alto, CA, USA. fbk@stanford.edu
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
|