Composition of colonic microbes in mice deficient in intestinal Treg subsets
Ontology highlight
ABSTRACT:
PROVIDER: PRJNA1010695 | ENA |
REPOSITORIES: ENA
Dataset's files
| Action | DRS | |||
|---|---|---|---|---|
| SRR25791015_1.fastq.gz | Fastqsanger.gz | |||
| SRR25791015_2.fastq.gz | Fastqsanger.gz | |||
| SRR25791016_1.fastq.gz | Fastqsanger.gz | |||
| SRR25791016_2.fastq.gz | Fastqsanger.gz | |||
| SRR25791017_1.fastq.gz | Fastqsanger.gz |
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Project description:The colonic lamina propria contains a distinct population of Foxp3+ T regulatory cells (Tregs) that modulate responses to commensal microbes. Analysis of gene expression revealed that the transcriptome of colonic Tregs is distinct from splenic and other tissue Tregs. Rorγ and Helios in colonic Tregs mark distinct populations: Rorγ+Helios- or Rorγ-Helios+ Tregs. We uncovered an unanticipated role for Rorγ, a transcription factor generally considered to be antagonistic to Foxp3. Rorγ in colonic Tregs accounts for a small but specific part of the colon-specific Treg signature. Nrp1- Tregs were sorted from Foxp3-cre.Rorcfl/fl mice, which have a Treg-selective deletion of Rorc, or paired WT littermates. For low-input RNAseq, 1,000 TCRb+CD4+YFP(Foxp3)+Nrp1- cells were double-sorted into Trizol, RNA extracted and reverse-transcribed using ArrayScript (Ambion). To reduce variability at least three replicates were generated.
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