Genome-wide expression profiling during protection from colitis by regulatory T cells.

Nanna Ny Kristensen; Jørgen Olsen; Monika Gad; Mogens Helweg Claesson

doi:10.1002/ibd.20277

Genome-wide expression profiling during protection from colitis by regulatory T cells.

Nanna Ny Kristensen, Jørgen Olsen, Monika Gad, Mogens Helweg Claesson

Institut for Cellulær og Molekylær Medicin

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

19 Citationer (Scopus)

Abstract

Udgivelsesdato: 2008-Jan

Originalsprog	Engelsk
Tidsskrift	Inflammatory Bowel Diseases
Vol/bind	14
Udgave nummer	1
Sider (fra-til)	75-87
Antal sider	12
ISSN	1078-0998
DOI	https://doi.org/10.1002/ibd.20277
Status	Udgivet - 2008

Bibliografisk note

Keywords: Animals; Colitis; Cytokines; Female; Gene Expression Profiling; Gene Expression Regulation; Intercellular Signaling Peptides and Proteins; Intestinal Mucosa; Mice; Mice, Inbred BALB C; Mice, SCID; Oligonucleotide Array Sequence Analysis; Receptors, Chemokine; Rectum; Reverse Transcriptase Polymerase Chain Reaction; T-Lymphocytes, Regulatory; Transcription Factors

Adgang til dokumentet

10.1002/ibd.20277

Citationsformater

@article{8ff10dd096cb11dd86a6000ea68e967b,

title = "Genome-wide expression profiling during protection from colitis by regulatory T cells.",

abstract = "BACKGROUND: In the adoptive transfer model of colitis it has been shown that regulatory T cells (Treg) can hinder disease development and cure already existing mild colitis. The mechanisms underlying this regulatory effect of CD4(+)CD25(+) Tregs are not well understood. METHODS: To identify pathways of importance for immune regulation in protected mice we studied the genome-wide expression profile in the inflamed rectum of SCID mice with CD4(+) T cell transfer colitis and in the uninflamed rectum of mice protected from colitis by Treg cells. We used DNA microarray technology (Affymetrix GeneChip Mouse Genome 430 2.0 Array), which enabled an analysis of a complete set of RNA transcript levels in each sample. Array results were confirmed by real-time reverse-transcriptase polymerase chain reaction (RT-PCR). RESULTS: Data were analyzed using combined projections to latent structures and functional annotation analysis. The colitic samples were clearly distinguishable from samples from normal mice by a vast number of inflammation- and growth factor-related transcripts. In contrast, the Treg-protected animals could not be distinguished from either the normal BALB/c mice or the normal SCID mice. mRNA expression profiles of cytokine, chemokine, and growth factor genes were significantly altered in colitic as opposed to noncolitic mice. In particular, the transcription factors STAT3, GATA2, and NFkappaB, the cytokine IL1beta, and the chemokine receptors CXCR3 and CCR1 as well as their ligands all seemingly play central roles in the inflammatory processes. CONCLUSIONS: We suggest that these molecules alone or in combination could be future therapeutic targets.",

author = "Kristensen, {Nanna Ny} and J{\o}rgen Olsen and Monika Gad and Claesson, {Mogens Helweg}",

note = "Keywords: Animals; Colitis; Cytokines; Female; Gene Expression Profiling; Gene Expression Regulation; Intercellular Signaling Peptides and Proteins; Intestinal Mucosa; Mice; Mice, Inbred BALB C; Mice, SCID; Oligonucleotide Array Sequence Analysis; Receptors, Chemokine; Rectum; Reverse Transcriptase Polymerase Chain Reaction; T-Lymphocytes, Regulatory; Transcription Factors",

year = "2008",

doi = "10.1002/ibd.20277",

language = "English",

volume = "14",

pages = "75--87",

journal = "Inflammatory Bowel Diseases",

issn = "1078-0998",

publisher = "Lippincott Williams & Wilkins",

number = "1",

}

TY - JOUR

T1 - Genome-wide expression profiling during protection from colitis by regulatory T cells.

AU - Kristensen, Nanna Ny

AU - Olsen, Jørgen

AU - Gad, Monika

AU - Claesson, Mogens Helweg

N1 - Keywords: Animals; Colitis; Cytokines; Female; Gene Expression Profiling; Gene Expression Regulation; Intercellular Signaling Peptides and Proteins; Intestinal Mucosa; Mice; Mice, Inbred BALB C; Mice, SCID; Oligonucleotide Array Sequence Analysis; Receptors, Chemokine; Rectum; Reverse Transcriptase Polymerase Chain Reaction; T-Lymphocytes, Regulatory; Transcription Factors

PY - 2008

Y1 - 2008

N2 - BACKGROUND: In the adoptive transfer model of colitis it has been shown that regulatory T cells (Treg) can hinder disease development and cure already existing mild colitis. The mechanisms underlying this regulatory effect of CD4(+)CD25(+) Tregs are not well understood. METHODS: To identify pathways of importance for immune regulation in protected mice we studied the genome-wide expression profile in the inflamed rectum of SCID mice with CD4(+) T cell transfer colitis and in the uninflamed rectum of mice protected from colitis by Treg cells. We used DNA microarray technology (Affymetrix GeneChip Mouse Genome 430 2.0 Array), which enabled an analysis of a complete set of RNA transcript levels in each sample. Array results were confirmed by real-time reverse-transcriptase polymerase chain reaction (RT-PCR). RESULTS: Data were analyzed using combined projections to latent structures and functional annotation analysis. The colitic samples were clearly distinguishable from samples from normal mice by a vast number of inflammation- and growth factor-related transcripts. In contrast, the Treg-protected animals could not be distinguished from either the normal BALB/c mice or the normal SCID mice. mRNA expression profiles of cytokine, chemokine, and growth factor genes were significantly altered in colitic as opposed to noncolitic mice. In particular, the transcription factors STAT3, GATA2, and NFkappaB, the cytokine IL1beta, and the chemokine receptors CXCR3 and CCR1 as well as their ligands all seemingly play central roles in the inflammatory processes. CONCLUSIONS: We suggest that these molecules alone or in combination could be future therapeutic targets.

AB - BACKGROUND: In the adoptive transfer model of colitis it has been shown that regulatory T cells (Treg) can hinder disease development and cure already existing mild colitis. The mechanisms underlying this regulatory effect of CD4(+)CD25(+) Tregs are not well understood. METHODS: To identify pathways of importance for immune regulation in protected mice we studied the genome-wide expression profile in the inflamed rectum of SCID mice with CD4(+) T cell transfer colitis and in the uninflamed rectum of mice protected from colitis by Treg cells. We used DNA microarray technology (Affymetrix GeneChip Mouse Genome 430 2.0 Array), which enabled an analysis of a complete set of RNA transcript levels in each sample. Array results were confirmed by real-time reverse-transcriptase polymerase chain reaction (RT-PCR). RESULTS: Data were analyzed using combined projections to latent structures and functional annotation analysis. The colitic samples were clearly distinguishable from samples from normal mice by a vast number of inflammation- and growth factor-related transcripts. In contrast, the Treg-protected animals could not be distinguished from either the normal BALB/c mice or the normal SCID mice. mRNA expression profiles of cytokine, chemokine, and growth factor genes were significantly altered in colitic as opposed to noncolitic mice. In particular, the transcription factors STAT3, GATA2, and NFkappaB, the cytokine IL1beta, and the chemokine receptors CXCR3 and CCR1 as well as their ligands all seemingly play central roles in the inflammatory processes. CONCLUSIONS: We suggest that these molecules alone or in combination could be future therapeutic targets.

U2 - 10.1002/ibd.20277

DO - 10.1002/ibd.20277

M3 - Journal article

C2 - 17924563

VL - 14

SP - 75

EP - 87

JO - Inflammatory Bowel Diseases

JF - Inflammatory Bowel Diseases

SN - 1078-0998

IS - 1

ER -