Targeting oncogene expression to endothelial cells induces proliferation of the myelo-erythroid lineage by repressing the notch pathway
- Authors
- Alghisi, E., Distel, M., Malagola, M., Anelli, V., Santoriello, C., Herwig, L., Krudewig, A., Henkel, C.V., Russo, D., and Mione, M.C.
- ID
- ZDB-PUB-130604-12
- Date
- 2013
- Source
- Leukemia 24(6): 943-53 (Journal)
- Registered Authors
- Anelli, Viviana, Distel, Martin, Mione, Marina, Santoriello, Cristina
- Keywords
- none
- Datasets
- GEO:GSE41988
- MeSH Terms
-
- Myeloid Cells/metabolism
- Myeloid Cells/pathology*
- Apoptosis
- Endothelium, Vascular/metabolism
- Endothelium, Vascular/pathology*
- Proto-Oncogene Protein c-fli-1
- Cell Differentiation
- Cell Transformation, Neoplastic/pathology*
- Receptor, Notch1/genetics
- Receptor, Notch1/metabolism*
- Proto-Oncogene Proteins/genetics*
- Proto-Oncogene Proteins/metabolism
- Animals
- RNA, Messenger/genetics
- Blotting, Western
- Erythroid Precursor Cells/metabolism
- Erythroid Precursor Cells/pathology*
- Zebrafish/genetics
- Zebrafish/metabolism
- Cell Proliferation*
- Hematopoiesis
- Humans
- Reverse Transcriptase Polymerase Chain Reaction
- ras Proteins/genetics*
- ras Proteins/metabolism
- Cell Lineage*
- Real-Time Polymerase Chain Reaction
- Fluorescent Antibody Technique
- PubMed
- 23625115 Full text @ Leukemia
Human oncogenes involved in the development of hematological malignancies have been widely used to model experimental leukemia. However, models of myeloid leukemia rarely reproduce the human disease in full, due to genetic complexity or to difficulties in targeting leukemia initiating cells. Here, we used a zebrafish genetic model to induce the expression of oncogenic RAS in endothelial cells, including the hemogenic endothelium of the dorsal aorta that generates hematopoietic cells, and observed the development of a myelo-erythroid proliferative disorder. In larvae, the phenotype is characterized by disruption of the vascular system and prominent expansion of the caudal hematopoietic tissue. In few surviving juveniles, increased number of immature hematopoietic cells and arrest of myeloid maturation was found in kidney marrow. Peripheral blood showed increased erythroblasts and myeloid progenitors. We found that the abnormal phenotype is associated with a downregulation of the Notch pathway, whereas overexpressing an activated form of Notch together with the oncogene prevents the expansion of the myelo-erythroid compartment. This study identifies the downregulation of the Notch pathway following an oncogenic event in the hemogenic endothelium as an important step in the pathogenesis of myelo-erythroid disorders and describes a number of potential effectors of this transformation.