Implant surface modification
by nanopatterning is an interesting
route for enhancing osseointegration in humans. Herein, the molecular
response to an intentional, controlled nanotopography pattern superimposed
on screw-shaped titanium implants is investigated in human bone. When
clinical implants are installed, additional two mini-implants, one
with a machined surface (M) and one with a machined surface superimposed
with a hemispherical nanopattern (MN), are installed in the posterior
maxilla. In the second-stage surgery, after 6–8 weeks, the
mini-implants are retrieved by unscrewing, and the implant-adherent
cells are subjected to gene expression analysis using quantitative
polymerase chain reaction (qPCR). Compared to those adherent to the
machined (M) implants, the cells adherent to the nanopatterned (MN)
implants demonstrate significant upregulation (1.8- to 2-fold) of
bone-related genes (RUNX2, ALP, and OC). No significant differences
are observed in the expression of the analyzed inflammatory and remodeling
genes. Correlation analysis reveals that older patient age is associated
with increased expression of proinflammatory cytokines (TNF-α
and MCP-1) on the machined implants and decreased expression of pro-osteogenic
factor (BMP-2) on the nanopatterned implants. Controlled nanotopography,
in the form of hemispherical 60 nm protrusions, promotes gene expressions
related to early osteogenic differentiation and osteoblastic activity
in implant-adherent cells in the human jaw bone.