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Dive into the research topics where Hideaki Nagura is active.

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Featured researches published by Hideaki Nagura.


Journal of Oral and Maxillofacial Surgery | 1988

Microangiographic and histologic evaluation of revascularization and healing after genioplasty by osteotomy of the inferior border of the mandible

Kenneth A. Storum; William H. Bell; Hideaki Nagura

Correlated microangiographic and histologic studies in adult rhesus monkeys indicate that a pedicled genioplasty involving osteotomy of the inferior mandibular border maintains circulation and osseous viability of the repositioned genial segment. Circulation to the dental pulps was also not discernibly affected when accomplished a minimum of 8 mm below the root apices.


Iubmb Life | 2001

IL‐1β Increases uPA and uPA Receptor Expression in Human Gingival Fibroblasts

Naomi Ogura; Makiko Tobe; Hiroyuki Tamaki; Hideaki Nagura; Yoshimitsu Abiko

The binding of urokinase‐type plasminogen activator (uPA) to its receptor (uPAR) in various cell types has been proposed as an important feature of many cellular processes requiring extracellular proteolysis, cell adhesion, motility, and invasion. uPAR attaches to the cell surface with a glycosylphophatidylinositol (GPI) anchor, and serves to localize and accelerate the proteolysis cascade. In this study, we examined both uPA and uPAR levels in human gingival fibroblasts treated with an inflammatory cytokine, interleukin‐1 β(IL‐1 β). PA activity in the cell lysate was increased by treatment with IL‐1 β. Further, PA activity released by phosphatidylinositol‐specific phospholipase C, which detaches the GPI anchor, was also increased by IL‐1 β. The activity was inhibited by amiloride, a specific inhibitor of uPA. In addition, IL‐1 βincreased the protein and mRNA levels of both uPA and uPAR in gingival fibroblasts. These findings suggest that the enhancement of uPA and uPAR levels by IL‐1 βmay play an important role in the progression of periodontal diseases through pericellular proteolysis, and subsequent cellular behavior.


Journal of Oral Pathology & Medicine | 2005

Tumor necrosis factor‐α increases chemokine gene expression and production in synovial fibroblasts from human temporomandibular joint

Naomi Ogura; Makiko Tobe; Hiroyuki Sakamaki; Hideaki Nagura; Yoshimitsu Abiko; Toshirou Kondoh


Journal of Oral Pathology & Medicine | 2002

Interleukin-1β induces interleukin-6 mRNA expression and protein production in synovial cells from human temporomandibular joint

Naomi Ogura; Makiko Tobe; Hiroyuki Sakamaki; Hiroaki Kujiraoka; Masakazu Akiba; Yoshimitsu Abiko; Hideaki Nagura


International Journal of Oral and Maxillofacial Surgery | 2002

Nerve sheath myxoma of the tongue in a child

T. Makino; Tadahiko Utsunomiya; Y. Kamino; Ryoki Kobayashi; Masahiko Fukumoto; Hiroshi Yamamoto; Hideaki Nagura


Journal of Oral and Maxillofacial Surgery | 2002

Interleukin-1β stimulates interleukin-8 production and gene expression in synovial cells from human temporomandibular joint

Makiko Tobe; Naomi Ogura; Yoshimitsu Abiko; Hideaki Nagura


Journal of Oral Science | 2001

Ankylosis of the temporomandibular joint caused by rheumatoid arthritis : a pathological study and review

Rie Kobayashi; Tadahiko Utsunomiya; Hirotsugu Yamamoto; Hideaki Nagura


Journal of Periodontology | 1999

Increase of urokinase-type plasminogen activator receptor expression in human gingival fibroblasts by Porphyromonas gingivalis lipopolysaccharide.

Naomi Ogura; Hideaki Nagura; Yoshimitsu Abiko


International Journal of Oral and Maxillofacial Surgery | 2001

Activities of plasminogen activator, plasmin and kallikrein in synovial fluid from patients with temporomandibular joint disorders

Hiroyuki Sakamaki; Naomi Ogura; H. Kujiraoka; M. Akiba; Yoshimitsu Abiko; Hideaki Nagura


Journal of Oral Pathology & Medicine | 2004

Interleukin-1beta increases RANTES gene expression and production in synovial fibroblasts from human temporomandibular joint.

Naomi Ogura; Makiko Tobe; Hiroyuki Sakamaki; Hideaki Nagura; H. Hosaka; M. Akiba; Yoshimitsu Abiko; Toshirou Kondoh

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