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Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s

ABSTRACT: Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s

PROVIDER: PRJNA909759 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR22561719.fastq.gz	Fastqsanger.gz
	SRR22561720.fastq.gz	Fastqsanger.gz
	SRR22561721.fastq.gz	Fastqsanger.gz
	SRR22561722.fastq.gz	Fastqsanger.gz
	SRR22561723.fastq.gz	Fastqsanger.gz

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Similar Datasets

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s

Project description:Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s

| PRJNA913925 | ENA

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s

Project description:Innate lymphoid cells (ILC) are similar to T helper (Th) cells in expression of cytokines and transcription factors. For example, RORγt is the lineage-specific transcription factor for both ILC3 and Th17 cells. However, the ILC counterpart for BCL6-expressing T follicular helper (Tfh) cells has not been defined. Here, we report that in the ILC compartment, BCL6 is selectively co-expressed with not only CXCR5, but also RORγt and CCR6 in ILC3 from multiple tissues. BCL6-deficient ILC3 produce enhanced levels of IL-17A and IL-22. More importantly, phenotypic and single-cell ATAC-seq analysis show that absence of BCL6 in mature ILC3 increases the numbers of ILC1 and transitional cells co-expressing ILC3 and ILC1 marker genes. A lineage-tracing experiment further reveals BCL6+ ILC3 to ILC1 trans-differentiation under steady state. Lastly, microbiota promote BCL6 expression in colonic CCR6+ ILC3, and thus reinforce their stability. Collectively, our data have demonstrated that CCR6+ ILC3 have both Th17 and Tfh programs and that BCL6 expression in these cells functions to maintain their lineage identity.

2022-12-27 | GSE221341 | GEO

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [16s rDNA]

2022-12-29 | GSE220437 | GEO

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [RNA-seq in vivo]

2022-12-29 | GSE220434 | GEO

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [16s rDNA]

Project description:Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [16s rDNA]

| PRJNA909767 | ENA

Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [RNA-seq in vivo]

Project description:Cell autonomous expression of Bcl6 is required to maintain lineage identity of mouse CCR6+ ILC3s [RNA-seq in vivo]

| PRJNA909757 | ENA

Bulk RNA-seq of CCR6+ ILC3s

Project description:To determine the function of STING in ILC3s, we performed bulk RNA sequencing on CCR6+ ILC3s sorted from the large intestine of naïve Sting1 f/f and ROR t-cre x Sting1 f/f mice.

2025-06-18 | GSE254245 | GEO

Cell autonomous expression of BCL6 is required to maintain lineage identity of mouse CCR6+ ILC3s.

Project description:Innate lymphoid cells (ILC) are similar to T helper (Th) cells in expression of cytokines and transcription factors. For example, RORγt is the lineage-specific transcription factor for both ILC3 and Th17 cells. However, the ILC counterpart for BCL6-expressing T follicular helper (Tfh) cells has not been defined. Here, we report that in the ILC compartment, BCL6 is selectively co-expressed with not only CXCR5 but also RORγt and CCR6 in ILC3 from multiple tissues. BCL6-deficient ILC3 produces enhanced levels of IL-17A and IL-22. More importantly, phenotypic and single-cell ATAC-seq analysis show that absence of BCL6 in mature ILC3 increases the numbers of ILC1 and transitional cells co-expressing ILC3 and ILC1 marker genes. A lineage-tracing experiment further reveals BCL6+ ILC3 to ILC1 trans-differentiation under steady state. Finally, microbiota promote BCL6 expression in colonic CCR6+ ILC3 and thus reinforce their stability. Collectively, our data have demonstrated that CCR6+ ILC3 have both Th17 and Tfh programs and that BCL6 expression in these cells functions to maintain their lineage identity.

| S-EPMC9856750 | biostudies-literature

Bulk RNA-seq of CCR6+ ILC3s

Project description:Bulk RNA-seq of CCR6+ ILC3s

| PRJNA1069070 | ENA

Microarray data of REV-ERBa-deficient CCR6+ ILC3

Project description:Microarray was used to determine transcriptional differences between Nr1d1+/+ CCR6+ ILC3s and Nr1d1-/- CCR6+ ILC3s isolated from small intestine lamina propria

2019-08-29 | GSE136557 | GEO

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