Takashi Okiji

Prof. Takashi Okiji

orcid

Research Focus & Metrics

Academic Career Length

40Years (1987-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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21 July 2011 in International Endodontic Journal
Verified
Journal Article
Closed access
PDF file
LHL. Han
L. Han
TOTakashi Okiji
Takashi Okiji

12 February 2013 in International Endodontic Journal
Verified
Journal Article
Closed access
PDF file
LHL. Han
L. Han
TOTakashi Okiji
Takashi Okiji

1 April 1998 in Critical Reviews in Oral Biology & Medicine
Verified
Journal Article
Open access
PDF file
MJM. Jontell
M. Jontell
TOTakashi Okiji
Takashi Okiji
UDU. Dahlgren
U. Dahlgren
GBG. Bergenholtz
G. Bergenholtz
Defense reactions of the dentin/pulp complex involve a variety of biological systems, in which the immune system plays a pivotal role. The knowledge of the organization and function of pulpal immunocompetent cells has been sparse, but in recent years a significant body of information of immune mechanisms in general has provided a footing for substantial new knowledge of the immune mechanisms of the dental pulp. The identification of pulpal dendritic cells (DCs) has generated research activities which have led to a concept of how an antigenic challenge may evoke a pulpal inflammatory response. Although DCs are not able to identify foreign antigens specifically, they provide necessary signals to activate T-lymphocytes which in turn will orchestrate other immunocompetent cells to mount the local immune defense of the dental pulp. The purpose of this review is to accent the organization and function of pulpal DCs and other tissue and cellular components and to provide a basis for how they may interact to instigate pulpal defense mechanisms.

28 December 2009 in International Journal of Dentistry
Verified
Journal Article
Open access
PDF file
TOTakashi Okiji
Takashi Okiji
KYKunihiko Yoshiba
Kunihiko Yoshiba
This paper aims to review the biological and physicochemical properties of mineral trioxide aggregate (MTA) with respect to its ability to induce reparative dentinogenesis, which involves complex cellular and molecular events leading to hard-tissue repair by newly differentiated odontoblast-like cells. Compared with that of calcium hydroxide-based materials, MTA is more efficient at inducing reparative dentinogenesis in vivo. The available literature suggests that the action of MTA is attributable to the natural wound healing process of exposed pulps, although MTA can stimulate hard-tissue-forming cells to induce matrix formation and mineralization in vitro. Physicochemical analyses have revealed that MTA not only acts as a “calcium hydroxide-releasing” material, but also interacts with phosphate-containing fluids to form apatite precipitates. MTA also shows better sealing ability and structural stability, but less potent antimicrobial activity compared with that of calcium hydroxide. The clinical outcome of direct pulp capping and pulpotomy with MTA appears quite favorable, although the number of controled prospective studies is still limited. Attempts are being conducted to improve the properties of MTA by the addition of setting accelerators and the development of new calcium silicate-based materials.

2 July 2016 in Congenital Anomalies
Verified
Journal Article
Closed access
PDF file
NKNobuyuki Kawashima
Nobuyuki Kawashima
TOTakashi Okiji
Takashi Okiji

1 August 2008 in Journal of Endodontics
Verified
Journal Article
Closed access
MKMomoko Kuratate
Momoko Kuratate
KYKunihiko Yoshiba
Kunihiko Yoshiba
YSYoshimi Shigetani
Yoshimi Shigetani
NYNagako Yoshiba
Nagako Yoshiba
Hayato OhshimaHayato Ohshima
Hayato Ohshima
TOTakashi Okiji
Takashi Okiji