Adhesion to fibronectin stimulates proliferation of wild-type and bcr/abl-transfected murine hematopoietic cells

Cells of most tissues require adhesion to a surface to grow. However, for hematopoietic cells, both stimulation and inhibition of proliferation by adhesion to extracellular matrix components have been described. Furthermore, it has been suggested that progenitor cells from chronic myelogenous leukem...

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Main Authors: Krämer, Alwin (Author) , Hörner, Susanne (Author) , Willer, Andreas (Author) , Frühauf, Stefan (Author) , Hochhaus, Andreas (Author) , Hallek, Michael (Author) , Hehlmann, Rüdiger (Author)
Format: Article (Journal)
Language:English
Published: March 2, 1999
In: Proceedings of the National Academy of Sciences of the United States of America
Year: 1999, Volume: 96, Issue: 5, Pages: 2087-2092
ISSN:1091-6490
DOI:10.1073/pnas.96.5.2087
Online Access:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1073/pnas.96.5.2087
Verlag, lizenzpflichtig, Volltext: https://www.pnas.org/content/96/5/2087
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Author Notes:Alwin Krämer, Susanne Hörner, Andreas Willer, Stefan Fruehauf, Andreas Hochhaus, Michael Hallek, and Rüdiger Hehlmann
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Summary:Cells of most tissues require adhesion to a surface to grow. However, for hematopoietic cells, both stimulation and inhibition of proliferation by adhesion to extracellular matrix components have been described. Furthermore, it has been suggested that progenitor cells from chronic myelogenous leukemia show decreased β1 integrin-mediated adhesion to fibronectin, resulting in increased proliferation and abnormal trafficking. However, we show here that the chronic myelogenous leukemia-specific fusion protein p210bcr/abl stimulates the expression of α5β1 integrins and induces adhesion to fibronectin when expressed in the myeloid cell line 32D.
Item Description:Gesehen am 28.01.2022
Physical Description:Online Resource
ISSN:1091-6490
DOI:10.1073/pnas.96.5.2087