GLUT1 is Highly Expressed in Cementoblasts but not in Osteoblasts

Cementum is a specialized mineralized tissue covering root surface of the tooth. Although the tissue's composition resembles bone, there are distinct structural and functional differences between the two mineralized tissues. In this study, the genes that are differentially expressed in putative...

Full description

Saved in:
Bibliographic Details
Published inConnective Tissue Research Vol. 46; no. 3; pp. 117 - 124
Main Authors Koike, Hirofumi, Uzawa, Katsuhiro, Grzesik, Wojciech J., Seki, Naohiko, Endo, Yosuke, Kasamatsu, Atsushi, Yamauchi, Mitsuo, Tanzawa, Hideki
Format Journal Article
LanguageEnglish
Published England Informa UK Ltd 01.01.2005
Taylor & Francis
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Cementum is a specialized mineralized tissue covering root surface of the tooth. Although the tissue's composition resembles bone, there are distinct structural and functional differences between the two mineralized tissues. In this study, the genes that are differentially expressed in putative cementoblasts (human cementum-derived cells [HCDCs]) compared with preosteoblastic cells (human bone marrow stromal cells [BMSCs]) were screened by two independent microarray systems, and some of the selected genes were further analyzed by quantitative real-time RT-PCR. The gene encoding glucose transporter 1 [GLUT1], which showed the greatest difference between the two groups by the latter analysis, was subjected to further analyses. High levels of the GLUT1 protein in HCDCs, but not in BMSCs, were detected by Western blotting and immunocytochemistry. Furthermore, intense immunoreactivities for GLUT1 were observed in cementoblasts and cementocytes but not in osteoblasts or osteocytes in human periodontal tissues. These results indicate that GLUT1 may play a role in cementogenesis and could serve as a biomarker to differentiate between cells of cementoblastic and osteoblastic lineage.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0300-8207
1521-0456
1607-8438
DOI:10.1080/03008200591008437