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Hematopoietic aging promotes cancer by fueling IL-1⍺-driven emergency myelopoiesis

ABSTRACT: Hematopoietic aging promotes cancer by fueling IL-1⍺-driven emergency myelopoiesis

PROVIDER: PRJNA1149693 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR30295700.fastq.gz	Fastqsanger.gz
	SRR30295701.fastq.gz	Fastqsanger.gz
	SRR30295702.fastq.gz	Fastqsanger.gz
	SRR30295703.fastq.gz	Fastqsanger.gz
	SRR30295704.fastq.gz	Fastqsanger.gz

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Hematopoietic aging promotes cancer by fueling IL-1⍺-driven emergency myelopoiesis

Project description:Age is a major risk factor for cancer, but how aging impacts tumor control remains unclear. Here, we establish that aging of the immune system, regardless of the age of the stroma and tumor, impacts lung cancer progression. Hematopoietic aging enhances emergency myelopoiesis, resulting in the local accumulation of myeloid progenitor-like cells in lung tumors. These cells are a major source of IL-1⍺ that drives the enhanced myeloid response. The age-associated decline of DNMT3A enhances IL-1⍺ production, and disrupting IL-1R1 signaling early during tumor development normalized myelopoiesis and slowed the growth of lung, colonic, and pancreatic tumors. In human tumors, we identified an enrichment for IL-1⍺-expressing monocyte-derived macrophages linked to age, poorer survival, and recurrence, unraveling how aging impacts cancer.

2024-10-23 | GSE275150 | GEO

Maternal IL-10 restricts fetal emergency myelopoiesis

Project description:Maternal IL-10 restricts fetal emergency myelopoiesis

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Maternal IL-10 restricts fetal emergency myelopoiesis [scRNA-seq]

Project description:Maternal IL-10 restricts fetal emergency myelopoiesis [scRNA-seq]

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Maternal IL-10 restricts fetal emergency myelopoiesis [scATAC-seq]

Project description:Maternal IL-10 restricts fetal emergency myelopoiesis [scATAC-seq]

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Maternal IL-10 restricts fetal emergency myelopoiesis [scATAC-seq]

Project description:We investigated how late fetal liver (FL) mouse hematopoieitic stem and progenitor cells (HSPC) respond to inflammation, with the hypothesis that deficits in engagement of emergency myelopoiesis (EM) pathways could limit neutrophil output and contribute to perinatal neutropenia, ultimately explaining the susceptibility of neonates to inflammation and infection. We show that fetal HSPCs are biased toward erythroid and lymphoid cell production at steady state and fail to mount classical EM responses in vivo. Despite being capable of responding to EM-inducing stimuli in vitro, we find that maternal factors like interleukin-10 (IL-10) restrict fetal HSPCs from activating EM pathways in utero. Accordingly, we find that loss of maternal IL-10 restores EM activation in fetal HSPCs but at a cost of premature parturition. These results reveal the evolutionary trade-off inherent in maternal anti-inflammatory responses that maintain pregnancy but render the fetus susceptible to infection.

2024-02-29 | GSE240914 | GEO

Maternal IL-10 restricts fetal emergency myelopoiesis [scRNA-seq]

2024-02-29 | GSE240913 | GEO

Maternal IL-10 restricts fetal emergency myelopoiesis [Bulk RNA-seq]

Project description:Maternal IL-10 restricts fetal emergency myelopoiesis [Bulk RNA-seq]

| PRJNA1005684 | ENA

Mature B cells and Mesenchymal Stem Cells control emergency myelopoiesis

Project description:Systemic inflammation halts lymphopoiesis and prioritizes myeloid cell production. How blood cell production switches from homeostasis to emergency myelopoiesis is incompletely understood. Here we show that Lymphotoxin-b receptor (LTbR) signaling in combination with TNF and IL1 receptor signaling in mesenchymal stem cells (MSCs) downregulates Il7 expression to shutdown lymphopoiesis during systemic inflammation. LTbR signaling in MSCs also promoted CCL2 production to enable inflammatory monocyte egress from the bone marrow. Furthermore, pharmacological or genetic blocking of Il7 downregulation in MSCs impaired myeloid cell production and egress, which reduced survival against systemic bacterial and viral infections. Interestingly, lymphotoxin a1b2 delivered by B-lineage cells, and specifically by mature B cells, contributed to promote Il7 downregulation and reduce MSC lymphopoietic activity. Our studies revealed an unexpected role for LTbR signaling in MSCs and identified mature B cells as an important regulator of emergency myelopoiesis.

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Maternal IL-10 restricts fetal emergency myelopoiesis [Bulk RNA-seq]

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Interleukin-10 causes interferon γ-dependent emergency myelopoiesis

Project description:Interleukin-10 causes interferon γ-dependent emergency myelopoiesis

| PRJNA721937 | ENA