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Heparan sulfate in perlecan promotes mouse atherosclerosis: roles in lipid permeability, lipid retention, and smooth muscle cell proliferation.

Tran-Lundmark, Karin (författare)
Karolinska Institutet
Tran, Phan-Kiet (författare)
Karolinska Institutet
Paulsson-Berne, Gabrielle (författare)
Karolinska Institutet
visa fler...
Fridén, Vincent, 1975 (författare)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Wallenberg Laboratory
Soininen, Raija (författare)
Tryggvason, Karl (författare)
Karolinska Institutet
Wight, Thomas N (författare)
Kinsella, Michael G (författare)
Borén, Jan, 1963 (författare)
Gothenburg University,Göteborgs universitet,Wallenberglaboratoriet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Wallenberg Laboratory,Institute of Medicine, Department of Molecular and Clinical Medicine
Hedin, Ulf (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
2008
2008
Engelska.
Ingår i: Circulation research. - 1524-4571. ; 103:1, s. 43-52
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Heparan sulfate (HS) has been proposed to be antiatherogenic through inhibition of lipoprotein retention, inflammation, and smooth muscle cell proliferation. Perlecan is the predominant HS proteoglycan in the artery wall. Here, we investigated the role of perlecan HS chains using apoE null (ApoE0) mice that were cross-bred with mice expressing HS-deficient perlecan (Hspg2(Delta3/Delta3)). Morphometry of cross-sections from aortic roots and en face preparations of whole aortas revealed a significant decrease in lesion formation in ApoE0/Hspg2(Delta3/Delta3) mice at both 15 and 33 weeks. In vitro, binding of labeled mouse triglyceride-rich lipoproteins and human LDL to total extracellular matrix, as well as to purified proteoglycans, prepared from ApoE0/Hspg2(Delta3/Delta3) smooth muscle cells was reduced. In vivo, at 20 minutes influx of human (125)I-LDL or mouse triglyceride-rich lipoproteins into the aortic wall was increased in ApoE0/Hspg2(Delta3/Delta3) mice compared to ApoE0 mice. However, at 72 hours accumulation of (125)I-LDL was similar in ApoE0/Hspg2(Delta3/Delta3) and ApoE0 mice. Immunohistochemistry of lesions from ApoE0/Hspg2(Delta3/Delta3) mice showed decreased staining for apoB and increased smooth muscle alpha-actin content, whereas accumulation of CD68-positive inflammatory cells was unchanged. We conclude that the perlecan HS chains are proatherogenic in mice, possibly through increased lipoprotein retention, altered vascular permeability, or other mechanisms. The ability of HS to inhibit smooth muscle cell growth may also influence development as well as instability of lesions.

Nyckelord

Actins
metabolism
Animals
Antigens
CD
metabolism
Antigens
Differentiation
Myelomonocytic
metabolism
Aorta
metabolism
pathology
Apolipoproteins B
metabolism
Apolipoproteins E
genetics
metabolism
Atherosclerosis
genetics
metabolism
pathology
Capillary Permeability
genetics
Cell Proliferation
Crosses
Genetic
Disease Models
Animal
Heparan Sulfate Proteoglycans
genetics
metabolism
Heparitin Sulfate
genetics
metabolism
Humans
Inflammation
genetics
metabolism
pathology
Lipoproteins
LDL
metabolism
Mice
Mice
Knockout
Myocytes
Smooth Muscle
metabolism
pathology
Protein Binding
genetics
Triglycerides
metabolism

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