Glucose uptake mediated by glucose transporter 1 is essential for early tooth morphogenesis and size determination of murine molars

被引:28
作者
Ida-Yonemochi, Hiroko [1 ]
Nakatomi, Mitsushiro [1 ]
Harada, Hidemitsu [2 ]
Takata, Hiroki [3 ]
Baba, Otto [4 ]
Ohshima, Hayato [1 ]
机构
[1] Niigata Univ, Div Anat & Cell Biol Hard Tissue, Dept Tissue Regenerat & Reconstruct, Grad Sch Med & Dent Sci,Chuo Ku, Niigata 9518514, Japan
[2] Iwate Med Univ, Div Dev Biol & Regenerat Med, Dept Anat, Yahaba, Iwate 0283694, Japan
[3] Ezaki Glico Co Ltd, Inst Hlth Sci, Nishiyodogawa Ku, Osaka, Japan
[4] Tokyo Med & Dent Univ, Sect Biostruct Sci, Dept Hard Tissue Engn, Grad Sch,Bunkyo Ku, Tokyo 1138549, Japan
关键词
Glucose; Glucose transporter; Odontogenesis; Phloretin; Mice (ICR); PHLORETIN-INDUCED APOPTOSIS; ENAMEL KNOT; TRANSPORTER PROTEIN; MESSENGER-RNA; MOUSE MOLAR; RAT-BRAIN; IN-VITRO; INHIBITION; CELLS; EXPRESSION;
D O I
10.1016/j.ydbio.2011.12.020
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
Glucose is an essential source of energy for body metabolism and is transported into cells by glucose transporters (GLUTs). Well-characterized class I GLUT is subdivided into GLUTs1-4, which are selectively expressed depending on tissue glucose requirements. However, there is no available data on the role of GLUTs during tooth development. This study aims to clarify the functional significance of class I GLUT during murine tooth development using immunohistochemistry and an in vitro organ culture experiment with an inhibitor of GLUTs1/2, phloretin, and Glut1 and Glut2 short interfering RNA (siRNA). An intense GLUT1-immunoreaction was localized in the enamel organ of bud-stage molar tooth germs, where the active cell proliferation occurred. By the bell stage, the expression of GLUT1 in the dental epithelium was dramatically decreased in intensity, and subsequently began to appear in the stratum intermedium at the late bell stage. On the other hand, GLUT2-immunoreactivity was weakly observed in the whole tooth germs throughout all stages. The inhibition of GLUTs1/2 by phloretin in the bud-stage tooth germs induced the disturbance of primary enamel knot formation, resulting in the developmental arrest of the explants and the squamous metaplasia of dental epithelial cells. Furthermore, the inhibition of GLUTs1/2 in cap-to-bell-stage tooth germs reduced tooth size in a dose dependent manner. These findings suggest that the expression of GLUT1 and GLUT2 in the dental epithelial and mesenchymal cells seems to be precisely and spatiotemporally controlled, and the glucose uptake mediated by GLUT1 plays a crucial role in the early tooth morphogenesis and tooth size determination. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:52 / 61
页数:10
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