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Functionally distinct subset of monocytes in mouse and human blood [RNA-Seq]

ABSTRACT: Functionally distinct subset of monocytes in mouse and human blood [RNA-Seq]

PROVIDER: PRJNA625029 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR11539549.fastq.gz	Fastqsanger.gz
	SRR11539550.fastq.gz	Fastqsanger.gz
	SRR11539551.fastq.gz	Fastqsanger.gz
	SRR11539552.fastq.gz	Fastqsanger.gz
	SRR11539553.fastq.gz	Fastqsanger.gz

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Functionally distinct subset of monocytes in mouse and human blood

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Functionally distinct subset of monocytes in mouse and human blood

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

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Alternatively activated macrophages derived from monocytes and tissue macrophages are phenotypically and functionally distinct

Project description:Macrophages adopt an alternatively activated phenotype (AAM) when activated by IL-4. While these AAMs can be derived from local proliferation of resident tissue macrophages or recruited inflammatory monocytes, it is not known whether these different AAMs are phenotypically and functionally distinct. Using microarray analysis of gene expression, we demonstrated that while both monocyte- and tissue-derived AAM expressed high levels of Arg1, Chi3l3 and Retnla, only monocyte-derived AAM upregulated Raldh2 and PD-L2. The distinction between monocyte- and tissue-derived macrophages can, therefore, be made using different phenotypic markers. Gene expression profiling analysis with whole genome microarray of tissue-derived and monocyte-derived macrophages, induced using IL-4c and/or 4% thioglycollate.

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Human blood monocytes scRNAseq

Project description:Human blood monocytes scRNAseq

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Alternatively activated macrophages derived from monocytes and tissue macrophages are phenotypically and functionally distinct

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SuperSAGE evidence for CD14++CD16+ monocytes as a third monocyte subset

Project description:Monocytes are a heterogeneous cell population with subset-specific functions and phenotypes. The differential expression of CD14 and CD16 distinguishes classical CD14++CD16-, intermediate CD14++CD16+ and non-classical CD14+CD16++ monocytes. However, CD14++CD16+ monocytes remain the most poorly characterized subset so far. Therefore we analyzed the transcriptomes of the three monocyte subsets using SuperSAGE in combination with high-throughput sequencing. Analysis of 5,487,603 tags revealed unique identifiers of CD14++CD16+ monocytes, delineating these cells from the two other monocyte subsets. CD14++CD16+ monocytes were linked to antigen processing and presentation (e.g. CD74, HLA-DR, IFI30, CTSB), to inflammation and monocyte activation (e.g. TGFB1, AIF1, PTPN6), and to angiogenesis (e.g. TIE2, CD105). Therefore we provide genetic evidence for a distinct role of CD14++CD16+ monocytes in human immunity. Human monocyte subsets (CD14++CD16-, CD14++CD16+, CD14+CD16++) were isolated from 12 healthy volunteers based on MACS technology. Total RNA from monocyte subsets was isolated and same aliquots from each donor and monocyte subset were matched for SuperSAGE. Three SuperSAGE libraries (CD14++CD16-, CD14++CD16+ and CD14+CD16++) were generated.

2011-07-24 | E-GEOD-30811 | biostudies-arrayexpress

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