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Adenoviral vector-mediated overexpression of serum amyloid A in apoA-I-deficient mice.
Webb, N R; de Beer, M C; van der Westhuyzen, D R; Kindy, M S; Banka, C L; Tsukamoto, K; Rader, D L; de Beer, F C.
Afiliación
  • Webb NR; Department of Internal Medicine, University of Kentucky Medical Center, Lexington 40536, USA.
J Lipid Res ; 38(8): 1583-90, 1997 Aug.
Article en En | MEDLINE | ID: mdl-9300780
Serum amyloid A (SAA) is an acute phase reactant that can become the predominant apolipoprotein of high density lipoprotein (HDL) during severe inflammatory states. However, the function of SAA is unknown. To study the ability of SAA to form HDL in the absence of apolipoprotein A-I, we expressed the mouse SAA pI 6.15 (CE/J) isoform in apolipoprotein A-I knock-out (apoA-I (-/-)) mice using a recombinant adenovirus. As a control, apoA-I (-/-) mice were injected with an adenovirus expressing human apoA-I. High level expression of plasma SAA was obtained in the absence of any endogenous acute phase SAA production. SAA expression increased plasma HDL cholesterol levels about 2-fold, but to a lesser extent than the expression of apoA-I (about 10-fold). The HDL particles isolated by density ultracentrifugation from SAA-expressing mice were heterogeneous in size and composition and rich in free cholesterol as well as apoE and apoA-IV. Of the SAA expressed in the plasma, only a small fraction (4%) was associated with HDL particles in contrast to expressed apoA-I, of which 62% was associated with HDL. We conclude that SAA is unable to substitute for apoA-I in HDL particle formation.
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Apolipoproteínas / Proteína Amiloide A Sérica / Apolipoproteína A-I Límite: Animals / Humans Idioma: En Revista: J Lipid Res Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos
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Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Apolipoproteínas / Proteína Amiloide A Sérica / Apolipoproteína A-I Límite: Animals / Humans Idioma: En Revista: J Lipid Res Año: 1997 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos