RhoA controls Wnt upregulation on microstructured titanium surfaces

Simone Lumetti, Silvia Mazzotta, Sara Ferrillo, Maddalena Piergianni, Marilina Piemontese, Giovanni Passeri, Guido Maria Macaluso* (Corresponding Author), Carlo Galli

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Rough topography enhances the activation of Wnt canonical signaling in vitro, and this mediates its effects on cell differentiation. However, the molecular mechanisms underlying topography-dependent control of Wnt signaling are still poorly understood. As the small GTPase RhoA controls cytoskeletal reorganization and actomyosin-induced tensional forces, we hypothesized that RhoA could affect the activation of Wnt signaling in cells on micropatterned titanium surfaces. G-LISA assay revealed that RhoA activation was higher in C2C12 cells on rough (SLA) surfaces under basal conditions than on smooth (Polished) titanium. Transfection with dominant negative RhoA decreased Wnt activation by normalized TCF-Luc activity on SLA, whilst transfection with constitutively active RhoA increased TCF-Luc activation on Polished titanium. One mM Myosin II inhibitor Blebbistatin increased RhoA activation but decreased Wnt activation on SLA surfaces, indicating that tension-generating structures are required for canonical Wnt modulation on titanium surfaces. Actin inhibitor Cytochalasin markedly enhanced RhoA and TCF-Luc activation on both surfaces and increased the expression of differentiation markers in murine osteoblastic MC3T3 cells. Taken together, these data show that RhoA is upregulated in cells on rough surfaces and it affects the activation of Wnt canonical signaling through Myosin II modulation.
Original languageEnglish
Article number401859
JournalBioMed Research International
Publication statusPublished - 14 May 2014

Bibliographical note

The authors would like to thank Straumann Institut AG (and in particular Dr. Appert and Dr. Molenberg), Basel, Switzerland, for kindly providing the titanium surfaces used in the present study. The authors are also grateful to Dr. Francesca Ravanetti and Professor Antonio Cacchioli for their precious advices and technical assistance. The authors would like to thank Dr. Klaus Hahn for sharing his RhoA isoforms through the Addgene plasmid public repository. The study was funded by Grant no. 839_2012 from the ITI Foundation (Basel, Switzerland).


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