Expression of γ-IFN responsive genes in scavenger receptor over-expressing monocytes is associated with xanthomatosis

We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and...

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Published inAtherosclerosis Vol. 138; no. 2; pp. 335 - 345
Main Authors Grewal, Thomas, Boudreau, Mathieu, Roy, Madeleine, Chamberland, Ann, Lefebvre, Chantal, Lavigne, Jaques, Davignon, Jean, Minnich, Anne
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ireland Ltd 01.06.1998
Elsevier
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Online AccessGet full text
ISSN0021-9150
1879-1484
DOI10.1016/S0021-9150(98)00048-3

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Abstract We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and activator of transcription (STAT1 α) in monocytes from the proband II-2. Expression of γ-interferon inducible protein 10 (IP-10), a STAT1 α-responsive gene and mediator of inflammatory response, was also abnormally expressed in the monocytes from II-2. Over-expression of both genes was restricted to monocytes from II-2 and was not observed in monocytes from the clinically unaffected family members, unlike that of SR. Gel retardation assays with THP-1 cell extracts identified γ-IFN inducible DNA binding activity to three potential STAT1 DNA binding elements in the human IP-10 promoter region from nucleotides −245 to −188. Taken together these results suggest that γ-interferon mediated cell activation is responsible for STAT1 α-induced transcription of the IP-10 gene in THP-1 macrophages as well as in monocytes from II-2. Analysis of monocytes from familial hypercholesterolemic (FH) subjects, who frequently develop xanthomatosis, revealed a significant number of subjects with elevated STAT1 α and IP-10 expression. Our data suggest that the inflammatory effects of γ-IFN signaling could play a role in foam cell formation and xanthomatosis.
AbstractList We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and activator of transcription (STAT1alpha) in monocytes from the proband II-2. Expression of gamma-interferon inducible protein 10 (IP-10), a STAT1alpha-responsive gene and mediator of inflammatory response, was also abnormally expressed in the monocytes from II-2. Over-expression of both genes was restricted to monocytes from II-2 and was not observed in monocytes from the clinically unaffected family members, unlike that of SR. Gel retardation assays with THP-1 cell extracts identified gamma-IFN inducible DNA binding activity to three potential STATI DNA binding elements in the human IP-10 promoter region from nucleotides - 245 to - 188. Taken together these results suggest that gamma-interferon mediated cell activation is responsible for STAT1alpha-induced transcription of the IP-10 gene in THP-1 macrophages as well as in monocytes from II-2. Analysis of monocytes from familial hypercholesterolemic (FH) subjects, who frequently develop xanthomatosis, revealed a significant number of subjects with elevated STAT1alpha and IP-10 expression. Our data suggest that the inflammatory effects of gamma-IFN signaling could play a role in foam cell formation and xanthomatosis.
We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and activator of transcription (STAT1 α) in monocytes from the proband II-2. Expression of γ-interferon inducible protein 10 (IP-10), a STAT1 α-responsive gene and mediator of inflammatory response, was also abnormally expressed in the monocytes from II-2. Over-expression of both genes was restricted to monocytes from II-2 and was not observed in monocytes from the clinically unaffected family members, unlike that of SR. Gel retardation assays with THP-1 cell extracts identified γ-IFN inducible DNA binding activity to three potential STAT1 DNA binding elements in the human IP-10 promoter region from nucleotides −245 to −188. Taken together these results suggest that γ-interferon mediated cell activation is responsible for STAT1 α-induced transcription of the IP-10 gene in THP-1 macrophages as well as in monocytes from II-2. Analysis of monocytes from familial hypercholesterolemic (FH) subjects, who frequently develop xanthomatosis, revealed a significant number of subjects with elevated STAT1 α and IP-10 expression. Our data suggest that the inflammatory effects of γ-IFN signaling could play a role in foam cell formation and xanthomatosis.
We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and activator of transcription (STAT1alpha) in monocytes from the proband II-2. Expression of gamma-interferon inducible protein 10 (IP-10), a STAT1alpha-responsive gene and mediator of inflammatory response, was also abnormally expressed in the monocytes from II-2. Over-expression of both genes was restricted to monocytes from II-2 and was not observed in monocytes from the clinically unaffected family members, unlike that of SR. Gel retardation assays with THP-1 cell extracts identified gamma-IFN inducible DNA binding activity to three potential STATI DNA binding elements in the human IP-10 promoter region from nucleotides - 245 to - 188. Taken together these results suggest that gamma-interferon mediated cell activation is responsible for STAT1alpha-induced transcription of the IP-10 gene in THP-1 macrophages as well as in monocytes from II-2. Analysis of monocytes from familial hypercholesterolemic (FH) subjects, who frequently develop xanthomatosis, revealed a significant number of subjects with elevated STAT1alpha and IP-10 expression. Our data suggest that the inflammatory effects of gamma-IFN signaling could play a role in foam cell formation and xanthomatosis.We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of whom displayed extensive xanthomatosis. Using mRNA differential display we demonstrated abnormally high expression of the signal transducer and activator of transcription (STAT1alpha) in monocytes from the proband II-2. Expression of gamma-interferon inducible protein 10 (IP-10), a STAT1alpha-responsive gene and mediator of inflammatory response, was also abnormally expressed in the monocytes from II-2. Over-expression of both genes was restricted to monocytes from II-2 and was not observed in monocytes from the clinically unaffected family members, unlike that of SR. Gel retardation assays with THP-1 cell extracts identified gamma-IFN inducible DNA binding activity to three potential STATI DNA binding elements in the human IP-10 promoter region from nucleotides - 245 to - 188. Taken together these results suggest that gamma-interferon mediated cell activation is responsible for STAT1alpha-induced transcription of the IP-10 gene in THP-1 macrophages as well as in monocytes from II-2. Analysis of monocytes from familial hypercholesterolemic (FH) subjects, who frequently develop xanthomatosis, revealed a significant number of subjects with elevated STAT1alpha and IP-10 expression. Our data suggest that the inflammatory effects of gamma-IFN signaling could play a role in foam cell formation and xanthomatosis.
Author Grewal, Thomas
Boudreau, Mathieu
Minnich, Anne
Chamberland, Ann
Lefebvre, Chantal
Davignon, Jean
Roy, Madeleine
Lavigne, Jaques
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Issue 2
Keywords EDTA, ethylenediaminetetraacetic acid
EGF, epidermal growth factor
Xanthoma
hGBP, human GTP-binding protein
Foam cell
AcLDL, acetylated LDL
IP-10, γ-interferon-inducible protein 10
MCP-1, monocyte chemoattractant protein-1
STAT1 α
Macrophage activation
GAS, γ-interferon activation site
M-CSF, monocyte-colony stimulating factor
PDGF, platelet derived growth factor
GAPDH, glyceraldehyde-3-phosphate dehydrogenase
LDL, low density lipoprotein
Scavenger receptor
SR, scavenger receptor
STAT, signal transducer and activator of transcription
NF- κB, nuclear factor- κB
PBS, phosphate buffered saline
IP-10
FH, familial hypercholesterolemia
LPDS, lipoprotein deficient serum
γ-Interferon
γ-IFN, γ-interferon
IL, interleukin
TNF α, tumor necrosis factor α
LPS, lipopolysaccharide
OxLDL, oxidized LDL
FCS, fetal calf serum
PMA, phorbol 12-myristate 13-acetate
Human
Cell culture
Xanthomatosis
Skin disease
Metabolic diseases
Lipids
Hyperlipoproteinemia
Gene expression
Hereditary
Enzymopathy
Genetic determinism
Spumous cell
Hypercholesterolemia
Gene
Complication
Hyperlipemia
Dyslipemia
Gamma interferon
Macrophage
Language English
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SSID ssj0004718
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Snippet We have recently described an inherited over-expression of the macrophage scavenger receptor (SR) in blood monocytes from members of a kindred, only two of...
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StartPage 335
SubjectTerms Adult
Aged
Biological and medical sciences
Cells, Cultured
Chemokine CXCL10
Chemokines, CXC - biosynthesis
Chemokines, CXC - genetics
Disorders of blood lipids. Hyperlipoproteinemia
Female
Foam cell
Gene Expression Regulation
Humans
Interferon-gamma - metabolism
Interferon-Stimulated Gene Factor 3
IP-10
Macrophage activation
Male
Medical sciences
Membrane Proteins
Metabolic diseases
Middle Aged
Monocytes - metabolism
Receptors, Immunologic - biosynthesis
Receptors, Lipoprotein
Receptors, Scavenger
RNA, Messenger - analysis
Scavenger receptor
Scavenger Receptors, Class B
STAT1 α
Transcription Factors - biosynthesis
Transcription Factors - genetics
Xanthoma
Xanthomatosis - blood
Xanthomatosis - genetics
γ-Interferon
Title Expression of γ-IFN responsive genes in scavenger receptor over-expressing monocytes is associated with xanthomatosis
URI https://dx.doi.org/10.1016/S0021-9150(98)00048-3
https://www.ncbi.nlm.nih.gov/pubmed/9690917
https://www.proquest.com/docview/80047723
Volume 138
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