歯周組織再生を促すチタンナノ表面を開発―ナノテクノロジーにより歯周組織再生の鍵を握る細胞を制御―

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2026-05-14 東北大学

東北大学の研究グループは、歯周組織再生を促す新たなチタンナノ表面を開発した。天然歯では、歯根表面を覆うセメント質と歯根膜が歯と骨を結び、咀嚼時の力を吸収しているが、従来のインプラントにはこの構造がなく、生体機能の再現が課題だった。研究では、セメント質表面を模倣した三次元ナノ突起構造をチタン表面に形成し、セメント芽細胞への影響を解析。その結果、細胞外基質の石灰化が大幅に促進され、セメント質形成やリン酸代謝関連遺伝子の発現が活性化したほか、生体に近い結晶性ハイドロキシアパタイト形成も確認された。ナノ構造による物理刺激が細胞機能を制御したと考えられ、歯周組織を再構築できる次世代「バイオハイブリッド・インプラント」開発への応用が期待される。成果は『Dental Materials』に掲載された。

歯周組織再生を促すチタンナノ表面を開発―ナノテクノロジーにより歯周組織再生の鍵を握る細胞を制御―
図1. 三次元ナノ突起異方性構造の物理的接触刺激によるセメント芽細胞石灰化制御の概要

<関連情報>

異方性三次元チタンナノスパイク構造は、生物物理学的シグナルを介してヒトセメント芽細胞様細胞のマトリックス鉱化を促進する Anisotropic three-dimensional titanium nanospike architectures drive matrix mineralization of human cementoblast-like cells through biophysical cues

Kippei Ogumi, Masahiro Yamada, Koki Otake, Takayuki Ohtake, Jun Watanabe, Hiroshi Egusa
Dental Materials  Available online: 29 April 2026
DOI:https://doi.org/10.1016/j.dental.2026.04.012

Highlights

  • 3D anisotropically distributed titanium nanospikes enhanced human cementoblast-like cell mineralization.
  • Nanoscale architecture, not surface chemical properties, governed matrix mineralization.
  • Physical stimulation by nanospikes generated distinctive mechanotransduction signatures.
  • Rounded cell morphological changes predicted cementoblastic matrix mineralization.
  • 3D nanoscale architecture may also influence other physical surface properties.

Abstract

Objective

Regenerating cementum remains a major unmet challenge in periodontal and peri-implant therapy, underscoring the need to understand how cementoblasts respond to engineered surface cues. This study examined the manner in which titanium nanosurfaces integrating anisotropic nanopatterns with three-dimensional (3D) nanospike architectures regulate mechanotransduction and matrix mineralization in human cementoblast-like cells (hCEM).

Methods

Titanium surfaces with isotropic, anisotropic, and 3D anisotropic nanospike architectures were fabricated and characterized through quantitative analyses of nanoscale geometry and topographical organization. Surface chemistry and crystallinity were characterized using Fourier transform infrared spectroscopy, grazing-incidence X-ray diffraction, and X-ray photoelectron spectroscopy. hCEM cultures on each surface were evaluated for extracellular calcium (Ca) and phosphate (P) levels, Ca/P ratios, extracellular matrix crystallinity, cytomorphology, and phosphate metabolism-associated gene expression. Mechanotransduction activity was assessed through focal adhesion–Hippo pathway signaling. Relationships between nanoscale architecture, cell stimulation, morphology, and mineralization were examined using correlation and path analyses.

Results

Despite comparable wettability and oxide chemistry to that of other nanosurfaces, 3D anisotropic nanospike surfaces produced the highest mineralization and exhibited the highest Ca/P ratios, clear hydroxyapatite signatures, pronounced extracellular nodules, and coordinated activation of phosphate metabolism gene profiles. These surfaces induced prominent nanoscale vertex–cell interactions and distinct cytomorphological responses. Mineralization did not show association with vertical roughness, hydroxyl content, or crystallographic features but positively correlated (r = 0.94) with composite nanoscale architectural metrics capturing spatial heterogeneity and vertex density.

Significance

The finding that anisotropic 3D nanospike architectures are associated with enhanced matrix mineralization in human cementoblast-like cells under osteogenic conditions provides mechanistic insight into how nanoscale architecture modulates mineralization responses and may inform the design of cementum-targeted bioactive titanium surfaces.

医療・健康
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