Literature DB >> 1518819

Murine serum amyloid A3 is a high density apolipoprotein and is secreted by macrophages.

R L Meek1, N Eriksen, E P Benditt.   

Abstract

The serum amyloid A (SAA) proteins make up a multigene family of apolipoproteins associated with high density lipoproteins. They are of ancient origin; the finding of a highly homologous protein in mammals and ducks indicates that SAAs have been in existence for at least 300 million years. The interspecies similarity among the SAAs makes the mouse, in which they have been most thoroughly studied, a reasonable model to use for defining the function(s) of this family of proteins in humans. Originally it was observed that the SAA proteins were made in the liver and represented a set of proteins belonging to acute-phase reactants. SAA3 is a unique member of the SAA multigene family in mice in that its mRNA is also expressed in extrahepatic tissues by a variety of cell types, mainly macrophages and adipocytes. To date, nothing has been reported regarding the fate or function of the SAA3 translation product. To identify the SAA3 protein, we developed SAA3-specific antibodies by immunizing rabbits against a portion of SAA3 protein synthesized in a bacterial fusion protein expression system. Electroimmunoblot analysis of serum and lipoprotein fractions of it showed SAA3 to be associated with high density lipoproteins of mice treated with lipopolysaccharide. Furthermore, a continuous mouse macrophage cell line (J-774.1), when exposed to lipopolysaccharide, expressed SAA3 mRNA in a dose-dependent manner and secreted SAA3 protein. The expression and secretion of SAA3 by macrophages stimulated with lipopolysaccharide suggest a role for this SAA in local responses to injury and inflammation.

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Year:  1992        PMID: 1518819      PMCID: PMC49832          DOI: 10.1073/pnas.89.17.7949

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  31 in total

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Authors:  J P Segrest; H De Loof; J G Dohlman; C G Brouillette; G M Anantharamaiah
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Authors:  J F Oram; C J Johnson; T A Brown
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4.  The amphipathic alpha-helical repeats of apolipoprotein A-I are responsible for binding of high density lipoproteins to HepG2 cells.

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Journal:  J Biol Chem       Date:  1991-04-05       Impact factor: 5.157

5.  Amyloid protein SAA is associated with high density lipoprotein from human serum.

Authors:  E P Benditt; N Eriksen
Journal:  Proc Natl Acad Sci U S A       Date:  1977-09       Impact factor: 11.205

6.  The human acute-phase serum amyloid A gene family: structure, evolution and expression in hepatoma cells.

Authors:  J C Betts; M R Edbrooke; R V Thakker; P Woo
Journal:  Scand J Immunol       Date:  1991-10       Impact factor: 3.487

7.  Complete primary structures of two major murine serum amyloid A proteins deduced from cDNA sequences.

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Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

8.  Rat tissues express serum amyloid A protein-related mRNAs.

Authors:  R L Meek; E P Benditt
Journal:  Proc Natl Acad Sci U S A       Date:  1989-03       Impact factor: 11.205

9.  Changes in high density lipoprotein content following endotoxin administration in the mouse. Formation of serum amyloid protein-rich subfractions.

Authors:  J S Hoffman; E P Benditt
Journal:  J Biol Chem       Date:  1982-09-10       Impact factor: 5.157

10.  Endotoxin suppresses expression of apoprotein E by mouse macrophages in vivo and in culture. A biochemical and genetic study.

Authors:  Z Werb; J R Chin
Journal:  J Biol Chem       Date:  1983-09-10       Impact factor: 5.157

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6.  Acute-phase protein serum amyloid A3 is a novel paracrine coupling factor that controls bone homeostasis.

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7.  Protein profiling of isolated uterine AA amyloidosis causing fetal death in goats.

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Authors:  Erik R M Eckhardt; Jassir Witta; Jian Zhong; Razvan Arsenescu; Violeta Arsenescu; Yu Wang; Sarbani Ghoshal; Marcielle C de Beer; Frederick C de Beer; Willem J S de Villiers
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