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PMID: 6857276 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Combined lipase deficiency (cld): a lethal mutation on chromosome 17 of the mouse.

Science (New York, N.Y.) ·Vol. 221 ·No. 4606 ·1983-07-08 ·Pages 167-9

Paterniti JR, Brown WV, Ginsberg HN, Artzt K

Abstract

Two triglyceride lipases, lipoprotein lipase and hepatic triglyceride lipase, participate in the metabolism of plasma lipoproteins. A single recessive mutation, cld, on mouse chromosome 17 causes an apparent deficiency of both lipoprotein lipase and hepatic triglyceride lipase activities. Mice homozygous for this defect develop lethal hyperchylomicronemia within 2 days postpartum as a consequence of nursing. Plasma triglyceride values in affected mice often reach 20,000 milligrams per deciliter (100 times higher than that in normal littermates), and total lipase activity in plasma or tissues is 5 to 20 percent of that in controls.

MeSH Terms
Animals Cholesterol/blood Chromosomes Lipase/deficiency,genetics Lipoprotein Lipase/deficiency,genetics Lipoproteins/metabolism Mice Mutation Triglycerides/blood
Chemicals
Lipoproteins Triglycerides Cholesterol Lipase Lipoprotein Lipase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Paterniti J R
Brown W V
Ginsberg H N
Artzt K
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1983-07-08
Pages
167-9
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · CA 21651 · United States
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