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E-GEOD-51960

ABSTRACT: Tmod3-/- mouse fetal liver compared with wild type

OTHER RELATED OMICS DATASETS IN: PRJNA225937

PROVIDER: E-GEOD-51960 | ExpressionAtlas | 2015-07-27

REPOSITORIES: ExpressionAtlas

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Dataset's files

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			Action	DRS
	E-GEOD-51960-analysis-methods.tsv	Tabular
	E-GEOD-51960-atlasExperimentSummary.Rdata	Rdata
	E-GEOD-51960-configuration.xml	Xml
	E-GEOD-51960-percentile-ranks.tsv	Tabular
	E-GEOD-51960.condensed-sdrf.tsv	Tabular

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Project description:Tmod3-/- mouse fetal liver compared with wild type

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Microarray of Rnaseh2b KOF and RnaseH2b wild type fetal liver

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Transcript profiling of Lin-Sca-1+c-Kit+ (LSK) cells from mice reconstituted with wild type and necdin null fetal liver cells following a sublethal dose of irradiation (6,5 Gy)

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Deletion of Stk40 impairs definitive erythropoiesis in the mouse fetal liver

Project description:The serine threonine kinase Stk40 has been shown to involve in mouse embryonic stem cell differentiation, pulmonary maturation and adipocyte differentiation. Here we report that targeted deletion of Stk40 leads to fetal liver hypoplasia and anemia in the mouse embryos. The reduction of erythrocytes in the fetal liver is accompanied by increased apoptosis and compromised erythroid maturation. Stk40-/- fetal liver cells have significantly reduced colony forming units (CFUs) capable of erythroid differentiation, including burst forming unit-erythroid (BFU-E), colony forming unit-erythroid (CFU-E), and CFU-granulocyte, erythrocyte, megakaryocyte and macrophage (CFU-GEMM), but not CFU-granulocyte/macrophages (CFU-GM). Purified Stk40-/- megakaryocyte-erythrocyte progenitors (MEPs) produced substantially fewer CFU-E colonies compared to control cells. Moreover, Stk40-/- fetal liver erythroblasts failed to form normal erythroblastic islands in association with wild type or Stk40-/- macrophages, indicating an intrinsic defect of Stk40-/- erythroblasts. Furthermore, the hematopoietic stem and progenitor cell pool is reduced in Stk40-/- fetal livers but still retains the multi-lineage reconstitution capacity. Finally, analysis of microarray data of E14.5 fetal liver cells suggests a potential role of aberrantly activated TNF-α signaling in Stk40 depletion induced dyserythropoiesis with a concomitant increase in cleaved Caspase-3 and decrease in Gata1 proteins. Altogether, the identification of Stk40 as a regulator for fetal erythroid differentiation, maturation and survival provides new clues to the molecular regulation of erythropoiesis and related diseases.

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