Change of calpain and effect of mechanical stress on chondrocyte tube culture
Change of calpain and effect of mechanical stress on chondrocyte tube culture
批准号:
10671357
负责人:
NAKAGAWA Yasuaki
金额:
$2.11万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1998
资助国家:
日本
项目状态:
已结题
起止时间:
1998 至 1999
中文摘要
Rat chondrocyte cultures grown in centrifuge tubes with intermittent centrifugation differentiate into hypertrophic chondrocytes and form calcification。This culture system provides an extracellular matrix mineralization which is produced by chondrocytes per se,and we can assess this culture system as a model for the endochondral ossification in vivo.In our previous study,m-calpain was demonstrated immunohistichemically in epiphyseal chondrocytes,and immunoreactive m-calpain content in cells increased with terminal differentiation into hypertrophic cells。Using this culture system,we examined whether various degree of centrifugation changed the pattern of the endochondral ossification。Growth-plate chondrocytes were isolated from the rib cartilages of 5-week-old male Wister rats,and the cell suspension was transferred into a15-ml plastic centrifuge tube at a density of 16X10 I D14锡D1 cells/ml/tube and centrifuged at 1,500rpm for 5minutes。In the following,we divided three groups:group A was centrifuged at 3,000rpm for 30 minutes every day,group B was centrifuged at 1,500rpm for 5minutes every other day,and group C was added no centrifugation。Group C also had the increase of alkaline phosphatase activity and terminal differentiation like group A and B.There were no significant differences in DNA content,proteoglycan content and alkaline phosphatase activity of all three groups.Calcium content of group A was significantly larger than that of group B at3-week-culture,but at4-week-culture,there was no significant difference between them.
英文摘要
Rat chondrocyte cultures grown in centrifuge tubes with intermittent centrifugation differentiate into hypertrophic chondrocytes and form calcification. This culture system provides an extracellular matrix mineralization which is produced by chondrocytes per se, and we can assess this culture system as a model for the endochondral ossification in vivo. In our previous study, m-calpain was demonstrated immunohistichemically in epiphyseal chondrocytes, and immunoreactive m-calpain content in cells increased with terminal differentiation into hypertrophic cells. Using this culture system, we examined whether various degree of centrifugation changed the pattern of the endochondral ossification. Growth-plate chondrocytes were isolated from the rib cartilages of 5-week-old male Wister rats, and the cell suspension was transferred into a 15-ml plastic centrifuge tube at a density of 16X10ィイD14ィエD1 cells/ml/tube and centrifuged at 1, 500 rpm for 5 minutes. In the following, we divided three groups : group A was centrifuged at 3, 000 rpm for 30 minutes every day, group B was centrifuged at 1, 500 rpm for 5 minutes every other day, and group C was added no centrifugation. Group C also had the increase of alkaline phosphatase activity and terminal differentiation like group A and B. There were no significant differences in DNA content, proteoglycan content and alkaline phosphatase activity of all three groups. Calcium content of group A was significantly larger than that of group B at 3-week-culture, but at 4-week-culture, there was no significant difference between them.
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