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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 2 & 7

ABSTRACT: Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 2 & 7

PROVIDER: PRJNA937647 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR23584341.fastq.gz	Fastqsanger.gz
	SRR23584342.fastq.gz	Fastqsanger.gz
	SRR23584343.fastq.gz	Fastqsanger.gz
	SRR23584344.fastq.gz	Fastqsanger.gz

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 4

Project description:Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 4

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 1

Project description:Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 1

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 3 & 7

Project description:Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 3 & 7

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium

Project description:Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 1

Project description:Synovial Ly6c- cells are phenotypically distinct from circulating NCM

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 3 & 7

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 2 & 7

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium Figure 4

Project description:Extra-vascular tissue location confers phenotype of TR-MC

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Tissue-resident, extravascular Ly6c<sup>-</sup> monocytes are critical for inflammation in the synovium.

Project description:Monocytes are abundant immune cells that infiltrate inflamed organs. However, the majority of monocyte studies focus on circulating cells, rather than those in tissue. Here, we identify and characterize an intravascular synovial monocyte population resembling circulating non-classical monocytes and an extravascular tissue-resident monocyte-lineage cell (TR-MC) population distinct in surface marker and transcriptional profile from circulating monocytes, dendritic cells, and tissue macrophages that are conserved in rheumatoid arthritis (RA) patients. TR-MCs are independent of NR4A1 and CCR2, long lived, and embryonically derived. TR-MCs undergo increased proliferation and reverse diapedesis dependent on LFA1 in response to arthrogenic stimuli and are required for the development of RA-like disease. Moreover, pathways that are activated in TR-MCs at the peak of arthritis overlap with those that are downregulated in LFA1-/- TR-MCs. These findings show a facet of mononuclear cell biology that could be imperative to understanding tissue-resident myeloid cell function in RA.

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Tissue-resident, extravascular Ly6c- monocytes are critical for inflammation in the synovium

Project description:This SuperSeries is composed of the SubSeries listed below.

2023-08-15 | GSE225803 | GEO