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Dive into the research topics where Noriyuki Nagai is active.

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Featured researches published by Noriyuki Nagai.


Brain Research | 2005

The engraftment of transplanted bone marrow-derived cells into the olfactory epithelium

Hidetsugu Tsujigiwa; Kazunori Nishizaki; Takanori Teshima; Yasushi Takeda; Junko Yoshinobu; Ayako Takeuchi; Yorihisa Orita; Yuji Sugata; Hitoshi Nagatsuka; Noriyuki Nagai

To investigate whether bone marrow cells migrate and are engrafted into the olfactory epithelium and differentiate into olfactory neurons, bone marrow cells of green fluorescence protein (GFP) mice were transplanted into lethally irradiated recipient mice. Immunohistochemical staining was performed to evaluate the engraftment of donor bone marrow cells into the olfactory epithelium. Immunostaining for GFP was found initially in the olfactory epithelium 2 weeks after bone marrow reconstruction. The percentage of GFP positive cells increased up to 12 months after bone marrow reconstruction. Double staining for GFP and olfactory marker protein showed that a population of the GFP-positive cells had characteristics of olfactory neurons. These results demonstrate that bone marrow cells can be engrafted in the olfactory epithelium and then differentiate into olfactory neuron cells.


Virchows Archiv | 2005

Immunolocalization and distribution patterns of type IV collagen alpha chains in oral mucosal melanoma

Hitoshi Nagatsuka; Rosario Santos Rivera; Mehmet Gunduz; You-Jin Lee; Ryo Tamamura; Esra Gunduz; Ichiro Naito; Yoshikazu Sado; Noriyuki Nagai

The basement membrane (BM) is mainly composed of type IV collagen, which is composed of triple combinations of six distinct alpha (α) chains in a tissue-specific manner. The six collagen chain-specific antibodies (α1–α6) were used to examine the BMs of the oral epithelium (OE) and tumor clusters in oral mucosal melanoma (OMM). Eight OMM cases were examined. Results showed that the α1 and α2 chains were constantly detected at the BM of the normal OE as well as at the OE with atypical melanocytic proliferation and in invasive melanoma with nodular nests. The α1 and α2 chains were intermittently detected in in situ OMM, early invasive OMM and advanced invasive OMM with sheet-like nests. Gradual loss of α5 and α6 from the OE with atypical melanocyte through in situ OMM and early invasive OMM was observed. These findings suggest that changes in the immunolocalization and distribution patterns of type IV collagen α chains are associated with the progression of OMM. The distribution pattern of type IV collagen α chain varies depending on the architecture of the nest.


Virchows Archiv | 2005

Expression and localization of cartilage-specific matrix protein chondromodulin-I mRNA in salivary pleomorphic adenomas

Kimihide Kusafuka; Keisuke Nakano; Yuji Hiraki; Chisa Shukunami; Hitoshi Nagatsuka; Noriyuki Nagai; Tamiko Takemura; Yutaku Sakaguchi; Kazuichi Okazaki; Michi Kusafuka; Hiroko Hisha; Susumu Ikehara

Pleomorphic adenoma is the most common epithelial tumor in the salivary glands. This tumor frequently exhibits “mesenchyme”-like components, including myxoid or chondroid areas. Recently, using immunohistochemical techniques, we reported that cartilage-specific matrix protein, chondromodulin-I (ChM-I), was deposited on the inter-territorial matrix of the chondroid area in salivary pleomorphic adenomas and that ChM-I, which is also a strong angio-inhibitory factor, plays an important role in the avascular nature of the chondroid area and the chondroid formation in this type of tumor. To elucidate which cells express ChM-I mRNA in pleomorphic adenomas, we examined the expression and localization of ChM-I mRNA in this type of tumor using an in situ hybridization technique. Immunoreactivity for ChM-I was observed in the inter-territorial matrix of the chondroid area, especially around the lacunae, and in the cytoplasm of neoplastic myoepithelial cells of the myxoid element of pleomorphic adenomas. On in situ hybridization analysis, strong signals for ChM-I mRNA were detected in the cytoplasm of the lacuna cells of the chondroid element, and moderate to marked signals were observed in the cytoplasm of the neoplastic myoepithelial cells of the myxoid element. Signals for ChM-I mRNA were also seen in the cytoplasm of the spindle-shaped neoplastic myoepithelial cells in the transitional areas between the myxoid and chondroid elements of this tumor. Signals for ChM-I mRNA were not seen in the inner ductal cells or the fibrous element. These findings indicate that lacuna cells and neoplastic myoepithelial cells express ChM-I mRNA and that mature ChM-I, which lacuna cells and neoplastic myoepithelial cells translate, is deposited in the chondroid matrix of pleomorphic adenomas. In conclusion, lacuna cells and neoplastic myoepithelial cells express ChM-I mRNA ectopically in pleomorphic adenoma, and this plays an important role in chondroid formation and hypovascularity in this type of tumor.


Angle Orthodontist | 2005

Expression of Notch1 and Math1 in Mandibular Condyle Cartilage in Neonatal Mice

Takako Shimizu; Hidetsugu Tsujigiwa; Hitoshi Nagatsuka; Norimasa Okafuji; Saburo Kurihara; Noriyuki Nagai; Toshiyuki Kawakami

On the basis of the cellular morphological changes in the cartilaginous area, the mandibular condylar cartilage is histopathologically composed of four different cell layers--fibrous, proliferative, maturative, and hypertrophic. Reaction for Notch1 was present in the hypertrophic cells only. However, Math1 was locally distributed in the hypertrophic layer and partially in the proliferative layer. The expression patterns of Notch1 and Math1 were slightly different. These results suggest that the morphogenesis regulation factors of Notch1 and Math1 may play some role in mandibular condylar cartilage. Positive reactions to osteopontin, as a control, were detected in the cytoplasm of all layers, although they varied from published data.


Gene | 2005

Frequent deletion and down-regulation of ING4, a candidate tumor suppressor gene at 12p13, in head and neck squamous cell carcinomas

Mehmet Gunduz; Hitoshi Nagatsuka; Kadir Demircan; Esra Gunduz; Beyhan Cengiz; Mamoru Ouchida; Hidetsugu Tsujigiwa; Eiki Yamachika; Kunihiro Fukushima; Levent Beder; Satoshi Hirohata; Yoshifumi Ninomiya; Kazunori Nishizaki; Kenji Shimizu; Noriyuki Nagai


Journal of Oral Pathology & Medicine | 2005

Various immunostaining patterns of CD31, CD34 and endoglin and their relationship with lymph node metastasis in oral squamous cell carcinomas.

Hitoshi Nagatsuka; Kazuteru Hibi; Mehmet Gunduz; Hidetsugu Tsujigiwa; Ryou Tamamura; Toshio Sugahara; Akira Sasaki; Noriyuki Nagai


International Journal of Oncology | 2005

Genetic and epigenetic alterations of BRG1 promote oral cancer development

Esra Gunduz; Mehmet Gunduz; Mamoru Ouchida; Hitoshi Nagatsuka; Levent Beder; Hidetsugu Tsujigiwa; Kunihiro Fukushima; Kazunori Nishizaki; Kenji Shimizu; Noriyuki Nagai


Oral Oncology | 2005

Heparanase gene and protein expression in ameloblastoma: possible role in local invasion of tumor cells

Hitoshi Nagatsuka; Phuu Pwint Han; Hidetsugu Tsujigiwa; Chong Huat Siar; Mehmet Gunduz; Toshio Sugahara; Akira Sasaki; Motowo Nakajima; Yoshio Naomoto; Noriyuki Nagai


Dental Materials Journal | 2005

In Vivo Effect of Fluoride-substituted Apatite on Rat Bone

Miho Inoue; Hitoshi Nagatsuka; Hidetsugu Tsujigiwa; Masahisa Inoue; Racquel Z. LeGeros; Toshio Yamamoto; Noriyuki Nagai


Oral Oncology | 2005

Analysis of amelogenin gene (AMGX, AMGY) expression in ameloblastoma

Hidetsugu Tsujigiwa; Hitoshi Nagatsuka; Phuu Pwint Han; Mehmet Gunduz; Chong Huat Siar; Shinichiro Oida; Noriyuki Nagai

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Hidetsugu Tsujigiwa

Okayama University of Science

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