Osteoblast maturation on microtextured titanium involves paracrine regulation of bone morphogenetic protein signaling. Issue 5 (6th September 2014)

• Record Type: Journal Article
• Authors: Olivares‐Navarrete, Rene; Hyzy, Sharon L.; Pan, Qingfen; Dunn, Ginger; Williams, Joseph K.; Schwartz, Zvi; Boyan, Barbara D.
• Is Part Of: Journal of biomedical materials research. Volume 103:Issue 5(2015:May)
• Page Start: 1721
• Page End: 1731
• Publication Date: 2014-09-06
• Subjects: osteoblasts -- bone morphogenetic protein -- titanium -- surface roughness -- cell signaling; Biomedical materials -- Periodicals; 610.28
• DOI: 10.1002/jbm.a.35308
• Languages: English
• ISSNs: 1549-3296

Abstract

Abstract: Osteoblasts are sensitive to surface microtopography and chemistry. Osteoblast differentiation and maturation are higher in vitro and bone formation and osseointegration enhanced in vivo on microstructured titanium (Ti) compared to smooth surfaces. Cells increased BMP2 expression on microtextured Ti alloy, suggesting a paracrine role in regulating osteoblast maturation. However, recent studies show that exogenous BMP2 inhibits osteoblast production of anti‐inflammatory cytokines and osteocalcin, indicating that control of BMP‐signaling may be involved. This study examined whether cells modulate BMP ligands, receptors, and inhibitors during osteoblast maturation on Ti, specifically focusing on the roles of BMP2 and Noggin (NOG). mRNA and protein for BMP2, BMP4, and BMP7 and receptors BMPR1A, BMPR1B, and BMPR2, and BMP inhibitors were upregulated on microtextured surfaces in comparison to smooth surfaces. Maturation on microstructured Ti was slightly enhanced with exogenous BMP2 while NOG addition inhibited osteoblast maturation. Cells with NOG knocked down significantly increased osteoblast maturation. These results demonstrate that BMP‐related molecules are controlled during osteoblast maturation on microstructured Ti surfaces and that endogenous NOG is an important regulator of the process. Modifying paracrine BMP signaling may yield more robust bone formation than application of exogenous BMPs. © 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 1721–1731, 2015.