Nanoporous Titanium Implant Surface Accelerates Osteogenesis via the Piezo1/Acetyl-CoA/β-Catenin Pathway.

Nano Lett

State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration & National Clinical Research Center for Oral Diseases & Shaanxi International Joint Research Center for Oral Diseases, Department of General Dentistry and Emergency, School of Stomatology, Air Force Medical University, Xi'an 710032, China.

Published: July 2024

AI Article Synopsis

  • Osseointegration is crucial for implant success, and TiO nanotubes with surface modifications enhance bone formation.
  • The nanotubes' structure improves the adhesion, growth, and differentiation of stem cells by promoting mitochondrial functions.
  • This research reveals that the nanotubes activate signaling pathways that improve acetylation of β-catenin, supporting bone formation.

Article Abstract

Osseointegration is the most important factor determining implant success. The surface modification of TiO nanotubes prepared by anodic oxidation has remarkable advantages in promoting bone formation. However, the mechanism behind this phenomenon is still unintelligible. Here we show that the nanomorphology exhibited open and clean nanotube structure and strong hydrophilicity, and the nanomorphology significantly facilitated the adhesion, proliferation, and osteogenesis differentiation of stem cells. Exploring the mechanism, we found that the nanomorphology can enhance mitochondrial oxidative phosphorylation (OxPhos) by activating Piezo1 and increasing intracellular Ca. The increase in OxPhos can significantly uplift the level of acetyl-CoA in the cytoplasm but not significantly raise the level of acetyl-CoA in the nucleus, which was beneficial for the acetylation and stability of β-catenin and ultimately promoted osteogenesis. This study provides a new interpretation for the regulatory mechanism of stem cell osteogenesis by nanomorphology.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11247543PMC
http://dx.doi.org/10.1021/acs.nanolett.4c01101DOI Listing

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