Literature DB >> 3783088

Amyloid A gene family expression in different mouse tissues.

R L Meek, E P Benditt.   

Abstract

Serum amyloid A (SAA) is a major acute-phase reactant and apoprotein of high density lipoprotein (HDL). SAA is encoded by a family of three active genes. We examined hepatic expression and searched for extrahepatic expression of the three SAA mRNAs after injection with casein or LPS. Studies using an SAA cDNA, which detects all three SAA mRNAs, revealed that after casein injection liver SAA mRNA was elevated approximately 1,000-fold. Adrenal gland expressed SAA mRNA at a low level (0.5% of hepatic level), and was the only extrahepatic tissue with elevated SAA mRNA after casein injection. The small intestine, primarily the ileum, and the large intestine of unstimulated control animals contained 5- and 15-fold higher SAA mRNA levels than control liver. LPS also elevated liver SAA mRNA approximately 1,000-fold. However, in contrast to casein injection, every extrahepatic tissue examined expressed SAA mRNA. Lung and kidney contained 2-5% and large intestine contained nearly 10% of SAA mRNA levels found in liver RNA. SAA mRNA levels were lower in the remaining tissues and ranged from 0.1% in the brain and pancreas to 1.0% in the small intestine, with the ileum containing 50-fold more than the duodenum. Analysis of liver with SAA1, SAA2, and SAA3 mRNA-specific oligonucleotide probes revealed that SAA1 and SAA2 mRNA were elevated approximately 50-fold higher than SAA3 mRNA after casein administration. LPS, however, induced all three SAA mRNAs equally. In extrahepatic tissues, SAA1, SAA2, and SAA3 mRNAs were expressed differentially and can be grouped into three general classes: tissues expressing all three genes, tissues expressing SAA1 and SAA3, and tissues expressing predominantly or only SAA3.

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Year:  1986        PMID: 3783088      PMCID: PMC2188489          DOI: 10.1084/jem.164.6.2006

Source DB:  PubMed          Journal:  J Exp Med        ISSN: 0022-1007            Impact factor:   14.307


  41 in total

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Journal:  J Biol Chem       Date:  1986-06-25       Impact factor: 5.157

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Journal:  Am J Pathol       Date:  1965-12       Impact factor: 4.307

3.  Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose.

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Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

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Journal:  J Clin Invest       Date:  1972-10       Impact factor: 14.808

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Journal:  Nature       Date:  1980-06-12       Impact factor: 49.962

6.  Synthesis and secretion of serum amyloid protein A (SAA) by hepatocytes in mice treated with casein.

Authors:  M D Benson; E Kleiner
Journal:  J Immunol       Date:  1980-02       Impact factor: 5.422

7.  Isolation and partial characterization of SAA-an amyloid-related protein from human serum.

Authors:  C J Rosenthal; E C Franklin; B Frangione; J Greenspan
Journal:  J Immunol       Date:  1976-05       Impact factor: 5.422

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Journal:  Am J Pathol       Date:  1971-10       Impact factor: 4.307

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Authors:  T Maniatis; A Jeffrey; D G Kleid
Journal:  Proc Natl Acad Sci U S A       Date:  1975-03       Impact factor: 11.205

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Authors:  J D Sipe; S N Vogel; J L Ryan; K P McAdam; D L Rosenstreich
Journal:  J Exp Med       Date:  1979-09-19       Impact factor: 14.307

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  64 in total

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Authors:  X Li; W S Liao
Journal:  Nucleic Acids Res       Date:  1992-09-25       Impact factor: 16.971

2.  A novel cis-acting element is essential for cytokine-mediated transcriptional induction of the serum amyloid A gene in nonhepatic cells.

Authors:  A Ray; B K Ray
Journal:  Mol Cell Biol       Date:  1996-04       Impact factor: 4.272

3.  Mouse serum amyloid A protein. Complete amino acid sequence and mRNA analysis of a new isoform.

Authors:  M C de Beer; F C de Beer; C M Beach; I Carreras; J D Sipe
Journal:  Biochem J       Date:  1992-05-01       Impact factor: 3.857

4.  Serum amyloid A activates the NLRP3 inflammasome and promotes Th17 allergic asthma in mice.

Authors:  Jennifer L Ather; Karina Ckless; Rebecca Martin; Kathryn L Foley; Benjamin T Suratt; Jonathan E Boyson; Katherine A Fitzgerald; Richard A Flavell; Stephanie C Eisenbarth; Matthew E Poynter
Journal:  J Immunol       Date:  2011-05-27       Impact factor: 5.422

5.  Regulation of mouse serum amyloid A gene expression in transfected hepatoma cells.

Authors:  J H Huang; H Y Rienhoff; W S Liao
Journal:  Mol Cell Biol       Date:  1990-07       Impact factor: 4.272

6.  Hepatic serum amyloid A1 aggravates T cell-mediated hepatitis by inducing chemokines via Toll-like receptor 2 in mice.

Authors:  Young Rae Ji; Hei Jung Kim; Ki Beom Bae; Sanggyu Lee; Myoung Ok Kim; Zae Young Ryoo
Journal:  J Biol Chem       Date:  2015-04-06       Impact factor: 5.157

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

Authors:  Roman Thaler; Ines Sturmlechner; Silvia Spitzer; Scott M Riester; Monika Rumpler; Jochen Zwerina; Klaus Klaushofer; Andre J van Wijnen; Franz Varga
Journal:  FASEB J       Date:  2014-12-09       Impact factor: 5.191

8.  Serum amyloid A3 is pro-atherogenic.

Authors:  Joel C Thompson; Patricia G Wilson; Preetha Shridas; Ailing Ji; Maria de Beer; Frederick C de Beer; Nancy R Webb; Lisa R Tannock
Journal:  Atherosclerosis       Date:  2017-11-17       Impact factor: 5.162

9.  Serum amyloid A3 does not contribute to circulating SAA levels.

Authors:  Tsuyoshi Chiba; Chang Yeop Han; Tomas Vaisar; Kentaro Shimokado; Atil Kargi; Mei-Hsiu Chen; Shari Wang; Thomas O McDonald; Kevin D O'Brien; Jay W Heinecke; Alan Chait
Journal:  J Lipid Res       Date:  2009-03-12       Impact factor: 5.922

10.  Glomerular cell death and inflammation with high-protein diet and diabetes.

Authors:  Rick L Meek; Renee C LeBoeuf; Sandeep A Saha; Charles E Alpers; Kelly L Hudkins; Sheryl K Cooney; Robert J Anderberg; Katherine R Tuttle
Journal:  Nephrol Dial Transplant       Date:  2013-01-12       Impact factor: 5.992

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