N-Cadherin is expressed on human hematopoietic progenitor cells and mediates interaction with human mesenchymal stromal cells

Specific cell-cell junctions between hematopoietic stem cells (HSC) and their niche have been shown to regulate stem cell function. N-cadherin was suggested to play a central role in this process, whereas other studies indicated that it did not play an essential role in the murine model. We have ana...

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Main Authors: Wein, Frederik (Author) , Nkenmei-Pietsch, Larissa (Author) , Saffrich, Rainer (Author) , Wuchter, Patrick (Author) , Walenda, Thomas (Author) , Bork, Simone (Author) , Horn, Patrick (Author) , Diehlmann, Anke (Author) , Eckstein, Volker (Author) , Ho, Anthony Dick (Author) , Wagner, Wolfgang (Author)
Format: Article (Journal)
Language:English
Published: 4 January 2010
In: Stem cell research
Year: 2010, Volume: 4, Issue: 2, Pages: 129-139
ISSN:1876-7753
DOI:10.1016/j.scr.2009.12.004
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/j.scr.2009.12.004
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/S1873506109001421
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Author Notes:Frederik Wein, Larissa Pietsch, Rainer Saffrich, Patrick Wuchter, Thomas Walenda, Simone Bork, Patrick Horn, Anke Diehlmann, Volker Eckstein, Anthony D. Ho, Wolfgang Wagner
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Summary:Specific cell-cell junctions between hematopoietic stem cells (HSC) and their niche have been shown to regulate stem cell function. N-cadherin was suggested to play a central role in this process, whereas other studies indicated that it did not play an essential role in the murine model. We have analyzed the role of N-cadherin for interaction between hematopoietic progenitor cells (HPC) and supportive mesenchymal stromal cells (MSC) in a human-human setting. Expression of N-cadherin and of cadherin-11 (osteoblast cadherin) was analyzed in HPC by quantitative RT-PCR, Western blot, and flow cytometry. N-cadherin and cadherin-11 were expressed in HPC at a moderate level, whereas they were not detectable in differentiated cells. Confocal laser scanning microscopy revealed that N-cadherin and β-catenin are colocalized at the junction of HPC and MSC. siRNA knockdown of N-cadherin or cadherin-11 as well as treatment with the blocking function antibody decreased adhesive interaction of HPC to MSC. Furthermore, knockdown of N-cadherin or blocking function antibody impaired maintenance of long-term culture-initiating cells (LTC-IC) on coculture of HPC and MSC. These results indicate that N-cadherin is involved in the bidirectional interaction of human HPC with their cellular determinants in the niche.
Item Description:Gesehen am 24.10.2023
Physical Description:Online Resource
ISSN:1876-7753
DOI:10.1016/j.scr.2009.12.004