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 in | Atherosclerosis Vol. 138; no. 2; pp. 335 - 345 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Ireland Ltd
01.06.1998
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0021-9150 1879-1484 |
DOI | 10.1016/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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CitedBy_id | crossref_primary_10_1097_00041433_200110000_00003 crossref_primary_10_3892_ijmm_2013_1610 crossref_primary_10_1161_01_ATV_20_6_1565 crossref_primary_10_1161_01_ATV_21_5_825 crossref_primary_10_1016_j_atherosclerosis_2024_117507 |
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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 |
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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 |
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