Mechanical loading stimulates expression of connexin 43 in alveolar bone cells in the tooth movement model

被引:36
作者
Gluhak-Heinrich, J
Gu, SM
Pavlin, D
Jiang, JX
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Biochem, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Orthodont, San Antonio, TX 78229 USA
关键词
Cx43; gap junctions; mechanical loading of bone; tooth movement model;
D O I
10.1080/15419060600634619
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Bone osteoblasts and osteocytes express large amounts of connexin (Cx) 43, the component of gap junctions and hemichannels. Previous studies have shown that these channels play important roles in regulating biological functions in response to mechanical loading. Here, we characterized the distribution of mRNA and protein of Cx43 in mechanical loading model of tooth movement. The locations of bone formation and resorption have been well defined in this model, which provides unique experimental systems for better understanding of potential roles of Cx43 in bone formation and remodeling under mechanical stimulation. We found that mechanical loading increased Cx43 mRNA expression in osteoblasts and bone lining cells, but not in osteocytes, at both formation and resorption sites. Cx43 protein, however, increased in both osteoblasts and osteocytes in response to loading. Interestingly, the upregulation of Cx43 protein by loading was even more pronounced in osteocytes compared to other bone cells, with an appearance of punctate staining on the cell body and dendritic process. Cx45 was reported to be expressed in several bone cell lines, but here we did not detect the Cx45 protein in the alveolar bone cells. These results further suggest the potential involvement of Cx43-forming gap junctions and hemichannels in the process of mechanically induced bone formation and resorption.
引用
收藏
页码:115 / 125
页数:11
相关论文
共 44 条
[1]
FUNCTION OF OSTEOCYTES IN BONE [J].
AARDEN, EM ;
BURGER, EH ;
NIJWEIDE, PJ .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1994, 55 (03) :287-299
[2]
Oscillating fluid flow regulates gap junction communication in osteocytic MLO-Y4 cells by an ERK1/2 MAP kinase-dependent mechanism [J].
Alford, AI ;
Jacobs, CR ;
Donahue, HJ .
BONE, 2003, 33 (01) :64-70
[3]
Orthodontic movement induces high numbers of cells expressing IFN-γ at mRNA and protein levels [J].
Alhashimi, N ;
Frithiof, L ;
Brudvik, P ;
Bakhiet, M .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2000, 20 (01) :7-12
[4]
Mechanotransduction in bone - role of the lacuno-canalicular network [J].
Burger, EH ;
Klein-Nulend, J .
FASEB JOURNAL, 1999, 13 :S101-S112
[5]
Laboratory monitoring of surfactant imbibition with computerized tomography [J].
Chen, HL ;
Lucas, LR ;
Nogaret, LAD ;
Yang, HD ;
Kenyon, DE .
SPE RESERVOIR EVALUATION & ENGINEERING, 2001, 4 (01) :16-25
[6]
PGE2 is essential for gap junction-mediated intercellular communication between osteocyte-like MLO-Y4 cells in response to mechanical strain [J].
Cheng, BX ;
Kato, Y ;
Zhao, S ;
Luo, J ;
Sprague, E ;
Bonewald, LF ;
Jiang, JX .
ENDOCRINOLOGY, 2001, 142 (08) :3464-3473
[7]
Mechanical strain opens connexin 43 hemichannels in osteocytes: A novel mechanism for the release of prostaglandin [J].
Cherian, PP ;
Siller-Jackson, AJ ;
Gu, SM ;
Wang, X ;
Bonewald, LF ;
Sprague, E ;
Jiang, JX .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (07) :3100-3106
[8]
CANDIDATES FOR THE MECHANOSENSORY SYSTEM IN BONE [J].
COWIN, SC ;
MOSSSALENTIJN, L ;
MOSS, ML .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1991, 113 (02) :191-197
[9]
Expression pattern of connexin gene products at the early developmental stages of the mouse cardiovascular system [J].
Delorme, B ;
Dahl, E ;
JarryGuichard, T ;
Briand, JP ;
Willecke, K ;
Gros, D ;
TheveniauRuissy, M .
CIRCULATION RESEARCH, 1997, 81 (03) :423-437
[10]
Differentiation of human fetal osteoblastic cells and gap junctional intercellular communication [J].
Donahue, HJ ;
Li, ZY ;
Zhou, ZY ;
Yellowley, CE .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 278 (02) :C315-C322