The remodeling evaluation of osteopsathyrosis congenita adopting osteoclast-calvaria co-culture system in vitro
ZHANG Gao, ZHONG Qiao-Meng, YUAN Kai, CHEN Guo-Xian, LI Ji-Han, CHEN Jian-Ting
Chinese Journal of Clinical Anatomy ›› 2011, Vol. 29 ›› Issue (4) : 442-445.
The remodeling evaluation of osteopsathyrosis congenita adopting osteoclast-calvaria co-culture system in vitro
Objective To evaluate the effects of osteoblast (OB) and osteoclast (OC) on the bone remodeling of osteogenesis imperfecta (OI) adopting osteoclast-calvaria co-culture system in vitro on oim/oim (OI) mouse model. Methods Wild (WT) and OI mice were used and compared in this study. OC cells were cultured in calvaria (CAL) in vitro for WT (WTCAL-WTOC group) and OI mice (OICAL-OIOC group) respectively. Tartrate-resistant acid phosphatase (TRAP) staining and alkaline phosphatase (ALP) staining were used to identify OCs and OBs respectively. Bone resorption of OCs was assessed by the area percentage of absorption lacunam, which is the rate of OCs number to the whole calvarial surfaces. Results At the culturing time of d7, the number of OCs and OC/OB rate of group OICAL-OIOC were significantly lower than that of group WTCAL-WTOC. However, the OCs number normalized to resorption pit number was significantly greater in group OICAl-OIOC compared to that of WTCAl-WTOC group. Conclusions The mechanism of the increased OCs function is partially due to the increased bone turnover in OI mice model for the compensation of decreased OBs function.
Osteoclast / Bone remodeling / Osteogenesis imperfecta / Osteoclast-calvaria co-culture system
[1] Roughley PJ, Rauch F, Glorieux FH. Osteogenesis imperfecta--clinical and molecular diversity
[J]. Eur Cell Mater, 2003,30(5): 41-47.
[2] Rauch F, Glorieux FH. Treatment of children with osteogenesis imperfecta
[J]. Curr Osteoporos Rep, 2006, 4(4):159-164.
[3] Zeitlin L, Fassier F, Glorieux FH. Modern approach to children with osteogenesis imperfecta
[J]. J Pediatr Orthop B, 2003, 12(2):77-87.
[4] Rauch F, Travers R, Parfitt AM,et al. Static and dynamic bone histomorphometry in children with osteogenesis imperfecta
[J]. Bone, 2000, 26(6):581-589.
[5] Iwamoto J, Takeda T, Ichimura S. Increased bone resorption with decreased activity and increased recruitment of osteoblasts in osteogenesis imperfecta type I
[J]. J Bone Miner Metab, 2002,20(3):174-179.
[6] Zhang H, Doty SB, Dempster D, et al. Increased Early Resorption Activity and Alterations of Morphology in Osteoclasts Derived from the oim/oim Mouse Model of Osteogenesis Imperfecta (oim/oim)
[J]. J Cell Biol, 2007,102(4):1011-1020.
[7] Chipman SD, Sweet HO, McBride DJ Jr, et al. Defective pro alpha 2(I) collagen synthesis in a recessive mutation in mice: a model of human osteogenesis imperfect
[J]. Gene Therapy,1993,90(5):1701-1705.
[8] Stern PH, Krieger NS. Comparison of fetal rat limb bones and neonatal mouse calvaria: effects of parathyroid hormone and 1,25-dihydroxyvitamin D3
[J]. Calcif Tissue Int, 35(2):172-176.
[9] Hefley TJ, Krieger NS, Stern PH. Simultaneous measurement of bone resorption and collagen synthesis in neonatal mouse calvaria
[J]. Anal Biochem, 1986, 153(1):166-171.
[10] Murrills RJ, Stein LS, Fey CP, et al. The effects of parathyroid hormone (PTH) and PTH-related peptide on osteoclast resorption of bone slices in vitro: an analysis of pit size and the resorption focus
[J]. Endocrinology, 1990,127(6):2648-2653.
[11] Andersson MK, Lundberg P, Ohlin A, et al. Effects on osteoclast and osteoblast activities in cultured mouse calvarial bones by synovial fluids from patients with a loose joint prosthesis and from osteoarthritis patients
[J]. Arthritis Res Ther, 2007,9(1):R18.
[12] Kusano K, Miyaura C, Inada M, et al. Regulation of matrix metalloproteinases (MMP-2, -3, -9, and -13) by interleukin-1 and interleukin-6 in mouse calvaria: association of MMP induction with bone resorption
[J].Endocrinology, 1998,139(3):1338-1345.
[13] Baron R, Gertner JM, Lang R, et al. Increased bone turnover with decreased bone formation by osteoblasts in children with osteogenesis imperfecta tarda
[J]. Pediatr Res, 1983,17(3):204-207.
[14] Jones SJ, Glorieux FH, Travers R, et al. The microscopic structure of bone in normal children and patients with osteogenesis imperfecta: a survey using backscattered electron imaging
[J]. Calcif Tissue Int, 1999,64(1):8-17.
[15] Cepollaro C, Gonnelli S, Pondrelli C, et al. Osteogenesis imperfecta: bone turnover, bone density, and ultrasound parameters
[J]. Calcif Tissue Int, 1999, 65(2):129-132.
[16] McCarthy EF, Earnest K, Rossiter K, et al. Bone histomorphometry in adults with type IA osteogenesis imperfecta
[J]. Clin Orthop Relat Res, 1997, 336:254-262.
[17] Munns CF, Rauch F, Travers R, et al. Effects of intravenous pamidronate treatment in infants with osteogenesis imperfecta: clinical and histomorphometric outcome
[J]. J Bone Miner Res, 2005, 20(7):1235-1243.
[18] Rauch F, Travers R, Plotkin H,et al. The effects of intravenous pamidronate on the bone tissue of children and adolescents with osteogenesis imperfecta
[J]. J Clin Invest, 2002, 110(9):1293-1293.
[19]Ste-Marie LG, Charhon SA, Edouard C, et al. Iliac bone histomorphometry in adults and children with osteogenesis imperfecta
[J]. J Clin Pathol, 1984, 37(10):1081-1089.
[20]Kacena MA, Gundberg CM, Horowitz MC. A reciprocal regulatory interaction between megakaryocytes, bone cells, and hematopoietic stem cells
[J]. Bone, 2006, 39(5):978-984.
[21]Shapiro JR, McBride DJ Jr., Fedarko NS. OIM and related animal models of osteogenesis imperfecta
[J]. Connect Tissue Res, 1995,31(4):265-268.
[22]Cao J, Venton L, Sakata T,et al. Expression of RANKL and OPG Correlates with age-related bone loss in male C57BL/6 mice
[J]. J Bone Miner Res, 2003, 18(2): 270-277.
/
〈 |
|
〉 |