Phenotypic switching of in vitro mandibular condylar cartilage during matrix mineralization.

被引:5
作者
Inoue H. [1 ]
Hiraki Y. [1 ]
Nawa T. [1 ]
Ishizeki K. [1 ]
机构
[1] Department of Molecular Interaction and Tissue Engineering, Institute for Frontier Medical Sciences, Kyoto University, Kyoto
关键词
bone-marker genes; cell culture; chondrocyte; mandibular condyle; mineralization;
D O I
10.1046/j.0022-7722.2002.00031.x
中图分类号
学科分类号
摘要
In order to analyze the phenotypic conversion of chondrocytes, mandibular condyles of mice and rabbits were cultured under cell and organ culture systems, and then examined by a combination of morphological and biochemical procedures. In organ culture, mandibular condylar cartilage (MCC) obtained from newborn mice began to mineralize from the central zone and then progressively widened towards the peripheral zone. Electron microscopic observations showed that with the increasing duration of the organ culture, chondrocytes at the central zone converted into spindle-shaped osteoblastic cells accompanying the formation of the bone type of thick-banded collagen fibrils. To obtain a better understanding of the chondrocytic conversion, immunolocalizations for type I and type X collagens and osteocalcin (OC) were examined in mouse MCC cells in cell culture. Type X collagen and OC were expressed almost simultaneously at the late stage of culture, and type I collagen was detected along the calcified nodules after the production of these proteins. Northern blot analysis in cell cultures of rabbit MCC indicated that type II collagen and alkaline phosphatase (ALPase) messenger ribonucleic acids (mRNAs) were highly expressed at day 7, but subsequently decreased. In contrast, mRNA for type I collagen was expressed at a low level on day 7 and peaked on day 12. The present results suggest that, morphologically and biochemically, cellular modification in MCC cells under culture conditions occurs at a cellular morphological level and also at marker-gene-expression level.
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页码:237 / 246
页数:9
相关论文
共 126 条
[1]  
Ben-Ami YK(1993)Transformation of fetal secondary cartilage into embryonic bone in organ cultures of human mandibular condyle Cell Tissue Res 271 317-22
[2]  
von der Mark K(1946)A method for the rapid determination of alkaline phosphatase with five cubic millimeters of serum J Biol Chem 164 321-9
[3]  
Franzen A(1986)Isolation of the human gene for bone gla protein utilizing mouse and rat cDNA clones EMBO J 5 1885-90
[4]  
Bernard BD(1987)Single-step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction Ann Biochem 162 156-9
[5]  
Lunazz GC(1992)Hypertrophic chondrocytes undergo further differentiation in culture J Cell Biol 117 427-35
[6]  
Silbermann M(1990)Phenotypic changes of rabbit mandibular condylar cartilage cells in culture J Dent Res 69 1753-8
[7]  
Bessey OA(1994)Hypertrophic chondrocytes undergo further differentiation to osteoblast-like cells and participate in the initial bone formation in developing chick embryo J Bone Miner Res 9 1239-49
[8]  
Lowry OH(1979)Identification of O-phosphoserine, and γ -carboxyglutamic acid in the noncollagenous proteins ofbovine cementum: comparison with dentin enamel and bone Calcif Tissue Int 28 83-6
[9]  
Brock MM(1972)Immobilization and cartilage transformation into bone in the embryonic chick Anat Rec 173 391-404
[10]  
Celeste AJ(1977)Quantitative determination of γ carboxyglutamic acid in proteins Anal Biochem 80 212-23