Literature DB >> 3585176

Lipoprotein lipase in atherosclerosis: its presence in smooth muscle cells and absence from macrophages.

L Jonasson, G Bondjers, G K Hansson.   

Abstract

The localization of lipoprotein lipase (LPL) in human atherosclerotic lesions was studied with immunocytochemical techniques. In the fibrous cap and surrounding intima of the plaque, where the smooth muscle cell is the dominating cell type, a high number of cells reacted with anti-LPL. A much lower number of stained cells was seen in the central lipid core region where the macrophages dominate. Further characterization of the LPL-containing cells in tissue sections showed that most of them were smooth muscle cells. Only a minor fraction of the macrophages in the plaque contained the enzyme. The results were confirmed on isolated cells from atherosclerotic tissue. Lipoprotein lipase was also detected in smooth muscle cells of non-atherosclerotic arteries. These findings suggest that the smooth muscle cells are the major source of LPL in the vascular wall. However, the enzyme was not present in some of the smooth muscle cells in the atherosclerotic lesion. This may imply that LPL synthesis is down-regulated in the atherosclerotic plaque.

Entities:  

Mesh:

Substances:

Year:  1987        PMID: 3585176

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  9 in total

1.  Microarray analysis reveals novel gene expression changes associated with erectile dysfunction in diabetic rats.

Authors:  Chris J Sullivan; Thomas H Teal; Ian P Luttrell; Khoa B Tran; Mette A Peters; Hunter Wessells
Journal:  Physiol Genomics       Date:  2005-08-23       Impact factor: 3.107

Review 2.  The response-to-retention hypothesis of early atherogenesis.

Authors:  K J Williams; I Tabas
Journal:  Arterioscler Thromb Vasc Biol       Date:  1995-05       Impact factor: 8.311

3.  Lipoprotein lipase is synthesized by macrophage-derived foam cells in human coronary atherosclerotic plaques.

Authors:  K D O'Brien; D Gordon; S Deeb; M Ferguson; A Chait
Journal:  J Clin Invest       Date:  1992-05       Impact factor: 14.808

4.  Macrophages and smooth muscle cells express lipoprotein lipase in human and rabbit atherosclerotic lesions.

Authors:  S Ylä-Herttuala; B A Lipton; M E Rosenfeld; I J Goldberg; D Steinberg; J L Witztum
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-15       Impact factor: 11.205

5.  Expression of lipoprotein lipase mRNA and secretion in macrophages isolated from human atherosclerotic aorta.

Authors:  L Mattsson; H Johansson; M Ottosson; G Bondjers; O Wiklund
Journal:  J Clin Invest       Date:  1993-10       Impact factor: 14.808

6.  Rabbit aorta and human atherosclerotic lesions hydrolyze the sphingomyelin of retained low-density lipoprotein. Proposed role for arterial-wall sphingomyelinase in subendothelial retention and aggregation of atherogenic lipoproteins.

Authors:  S L Schissel; J Tweedie-Hardman; J H Rapp; G Graham; K J Williams; I Tabas
Journal:  J Clin Invest       Date:  1996-09-15       Impact factor: 14.808

7.  Restricted expression of homeobox genes distinguishes fetal from adult human smooth muscle cells.

Authors:  J M Miano; A B Firulli; E N Olson; P Hara; C M Giachelli; S M Schwartz
Journal:  Proc Natl Acad Sci U S A       Date:  1996-01-23       Impact factor: 11.205

8.  Lipoprotein lipase increases low density lipoprotein retention by subendothelial cell matrix.

Authors:  U Saxena; M G Klein; T M Vanni; I J Goldberg
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

9.  Transgenic rabbits expressing human lipoprotein lipase.

Authors:  M Araki; J Fan; M Challah; A Bensadoun; N Yamada; K Honda; T Watanabe
Journal:  Cytotechnology       Date:  2000-07       Impact factor: 2.058

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.