Differential bioactivity of four BMP-family members as function of biomaterial stiffness
Résumé
While a soft film itself is not able to induce cell spreading, BMP-2 presented via such soft film (so called
“matrix-bound BMP-2”) was previously shown to trigger cell spreading, migration and downstream BMP-2
signaling. Here, we used thin films of controlled stiffness presenting matrix-bound BMPs to study the effect
of four BMP members (BMP-2, 4, 7, 9) on cell adhesion and differentiation of skeletal progenitors. We
performed automated high content screening of cellular responses, including cell number, cell spreading area,
SMAD phosphorylation and alkaline phosphatase activity. We revealed that the cell response to bBMPs is
BMP-type specific and involved certain BMP receptors and beta chain integrins. In addition, this response is
stiffness-dependent for several receptors. The basolateral presentation of the BMPs allowed us to discriminate
the specificity of cellular response and the role of type I and II BMP receptors and of β integrins in a BMPtype
and stiffness-dependent manner. Notably, the role of BMP-2 and BMP-4 were found to have distinct
roles, while ALK5, previously known as a TGF-β receptor was revealed to be involved in the BMP-pathway.
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