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  Bone marrow niche-mimetics modulate HSPC function via integrin signaling

Kraeter, M., Jacobi, A., Otto, O., Tietze, S., Mueller, K., Poitz, D. M., et al. (2017). Bone marrow niche-mimetics modulate HSPC function via integrin signaling. SCIENTIFIC REPORTS, 7: 2549. doi:10.1038/s41598-017-02352-5.

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Kraeter, Martin1, Author
Jacobi, Angela1, Author
Otto, Oliver1, Author
Tietze, Stefanie1, Author
Mueller, Katrin1, Author
Poitz, David M.1, Author
Palm, Sandra1, Author
Zinna, Valentina M.1, Author
Biehain, Ulrike1, Author
Wobus, Manja1, Author
Chavakis, Triantafyllos1, Author
Werner, Carsten1, Author
Guck, Jochen2, Author           
Bornhauser, Martin1, Author
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1external, ou_persistent22              
2External Organizations, ou_persistent22              

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 Abstract: The bone marrow (BM) microenvironment provides critical physical cues for hematopoietic stem and progenitor cell (HSPC) maintenance and fate decision mediated by cell-matrix interactions. However, the mechanisms underlying matrix communication and signal transduction are less well understood. Contrary, stem cell culture is mainly facilitated in suspension cultures. Here, we used bone marrow-mimetic decellularized extracellular matrix (ECM) scaffolds derived from mesenchymal stromal cells (MSCs) to study HSPC-ECM interaction. Seeding freshly isolated HSPCs adherent (AT) and non-adherent (SN) cells were found. We detected enhanced expansion and active migration of AT-cells mediated by ECM incorporated stromal derived factor one. Probing cell mechanics, AT-cells displayed naive cell deformation compared to SN-cells indicating physical recognition of ECM material properties by focal adhesion. Integrin alpha IIb (CD41), alpha V (CD51) and beta 3 (CD61) were found to be induced. Signaling focal contacts via ITG beta 3 were identified to facilitate cell adhesion, migration and mediate ECM-physical cues to modulate HSPC function.

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Language(s): eng - English
 Dates: 2017
 Publication Status: Published online
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Type: -
 Identifiers: DOI: 10.1038/s41598-017-02352-5
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Title: SCIENTIFIC REPORTS
Source Genre: Journal
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Publ. Info: MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND : NATURE PUBLISHING GROUP
Pages: - Volume / Issue: 7 Sequence Number: 2549 Start / End Page: - Identifier: ISSN: 2045-2322