Abstract

The activation of p38alpha kinase mediates cell response to various extracellular factors including many interleukins and growth factors important for haematopoiesis. The role of p38alpha kinase was previously analysed in particular haematopoietic cells. In this study and for the first time, the role of p38alpha kinase in haematopoiesis was studied using a model of continuous haematopoietic development in pluripotent embryonic stem cells in vitro. The expression of transcripts associated with haematopoiesis and the potential for the formation of specific haematopoietic cell colonies were compared between wild-type and mutant p38alpha gene-depleted cells. The absence of p38alpha kinase led to the inhibition of hemangioblast formation during the first step of haematopoiesis. Later, during differentiation, due to the lack of p38alpha kinase, erythrocyte maturation was impaired. Mutant p38α−/− cells also exhibited decreased potential with respect to the expansion of granulocyte colony-forming units. This effect was reversed in the absence of erythropoietin as shown by colony-forming unit assay in media for colony-forming unit granulocytes/macrophages. p38alpha kinase thus plays an important role in the differentiation of common myeloid precursor cells into granulocyte lineages.

Highlights

  • Embryonic stem (ES) cells are derived from pluripotent cells of the inner cell mass of a blastocyst and have the potential to turn into cells of all three germ layers in the body

  • Mutant p38α−/ − cells exhibited decreased potential with respect to the expansion of granulocyte colonyforming units. This effect was reversed in the absence of erythropoietin as shown by colony-forming unit assay in media for colony-forming unit granulocytes/macrophages. p38alpha kinase plays an important role in the differentiation of common myeloid precursor cells into granulocyte lineages

  • The formation of hemangioblast is induced by the VEGF/Flk1/Etv2 signaling axis

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Summary

Introduction

Embryonic stem (ES) cells are derived from pluripotent cells of the inner cell mass of a blastocyst and have the potential to turn into cells of all three germ layers in the body. The differentiation of ES cells represents a unique in vitro model for the analysis of developmental processes. The hematopoietic specification of ES cells has been shown to recapitulate embryonic haematopoiesis [1, 2]. Haematopoiesis in embryonal development represents a complex of developmental process that involves several anatomical sites, after which HSCs that have arisen colonise bone marrow at birth. It has been shown that p38 kinase is involved in many other cellular responses including cell proliferation, differentiation, development, and apoptosis. It is known that in adults, p38α kinase is required for HSC activation as well as for the specification and maturation of hematopoietic cell lineages [9]. We hypothesized that p38α kinase plays a role in the development of hemangioblast and its differentiation into hematopoietic lineages. P38α regulates the differentiation of common myeloid progenitor (CMP) cells into granulocyte lineages

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