Unknown,Transcriptomics,Genomics,Proteomics

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A supporting environment for hematopoietic stem/progenitor cells is maintained by canonical Wnt signaling


ABSTRACT: Considerable information has accumulated about components of bone marrow that regulate survival, self-renewal and differentiation of hematopoietic cells. We have now studied Wnt signaling in that context, assessing influences on human and murine hematopoiesis. Microarray, PCR and staining experiments revealed that OP9 acquired osteoblastic characteristics while down-regulating some features associated with mesenchymal stem cells. This included down-regulation of Angiopoietin 1, c-Kit ligand and VCAM-1 expression. In contrast, production of decorin, tenascins and fibromodulin markedly increased. At least one of these extracellular matrix components, decorin is a regulator of hematopoiesis. That is, addition of the protein to OP9 co-cultures causes changes similar to Wnt3a. Two control samples (LZR1 & LZR2) were analyzed from OP9 mouse stromal cells transfected with vector only, and two experimental samples (W3A1 & W3A2) were analyzed from OP9 cells transfected with vector containing the Wnt3A gene.

ORGANISM(S): Mus musculus

SUBMITTER: Bart Frank 

PROVIDER: E-GEOD-30791 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

The canonical Wnt pathway shapes niches supportive of hematopoietic stem/progenitor cells.

Ichii Michiko M   Frank Mark Barton MB   Iozzo Renato V RV   Kincade Paul W PW  

Blood 20111123 7


Considerable information has accumulated about components of BM that regulate the survival, self-renewal, and differentiation of hematopoietic cells. In the present study, we investigated Wnt signaling and assessed its influence on human and murine hematopoiesis. Hematopoietic stem/progenitor cells (HSPCs) were placed on Wnt3a-transduced OP9 stromal cells. The proliferation and production of B cells, natural killer cells, and plasmacytoid dendritic cells were blocked. In addition, some HSPC char  ...[more]

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