中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2008年
10期
1311-1313
,共3页
周国顺%李雄峰%管国华%戴利成%蒋雪生%梅锦荣
週國順%李雄峰%管國華%戴利成%蔣雪生%梅錦榮
주국순%리웅봉%관국화%대리성%장설생%매금영
软骨细胞%脱噬作用%力学
軟骨細胞%脫噬作用%力學
연골세포%탈서작용%역학
Chondrocyte%Mechanics%Apoptosis
目的 探讨静水压对软骨细胞凋亡和增殖的影响及肿瘤坏死因子(TNF)-á和白细胞介素(IL)-1a与软骨细胞凋亡的关系.方法 兔膝关节软骨细胞放置在压力装置中采用不同持续时间(0、4、16、24h)和不同大小静水压力刺激(0、20、40、70 kp)后观察其凋亡及PCNA表达,测定相应细胞培养基中TNF-á和IL-1a的值.结果 软骨细胞受到不同大小静压力后,作用早期细胞凋亡显著(P<0.05),随时间延长凋亡值出现不同的变化.PCNA的表达在不同的压力下和对照组比较均有差异有统计学意义(P<0.05).TNF-á可重复双因素分析,时间和压力的交互作用(F=6.90,P<0.01).IL-1a可重复双因素分析,时间和压力的交互作用(F=5.80,P<0.01).结论 软骨细胞在持续高压力应力下凋亡增加,增殖减少;在持续低压力时出现相反的结果 .软骨细胞的凋亡和增殖和TNF-á和IL-1a变化有一定的相关性.
目的 探討靜水壓對軟骨細胞凋亡和增殖的影響及腫瘤壞死因子(TNF)-á和白細胞介素(IL)-1a與軟骨細胞凋亡的關繫.方法 兔膝關節軟骨細胞放置在壓力裝置中採用不同持續時間(0、4、16、24h)和不同大小靜水壓力刺激(0、20、40、70 kp)後觀察其凋亡及PCNA錶達,測定相應細胞培養基中TNF-á和IL-1a的值.結果 軟骨細胞受到不同大小靜壓力後,作用早期細胞凋亡顯著(P<0.05),隨時間延長凋亡值齣現不同的變化.PCNA的錶達在不同的壓力下和對照組比較均有差異有統計學意義(P<0.05).TNF-á可重複雙因素分析,時間和壓力的交互作用(F=6.90,P<0.01).IL-1a可重複雙因素分析,時間和壓力的交互作用(F=5.80,P<0.01).結論 軟骨細胞在持續高壓力應力下凋亡增加,增殖減少;在持續低壓力時齣現相反的結果 .軟骨細胞的凋亡和增殖和TNF-á和IL-1a變化有一定的相關性.
목적 탐토정수압대연골세포조망화증식적영향급종류배사인자(TNF)-á화백세포개소(IL)-1a여연골세포조망적관계.방법 토슬관절연골세포방치재압력장치중채용불동지속시간(0、4、16、24h)화불동대소정수압력자격(0、20、40、70 kp)후관찰기조망급PCNA표체,측정상응세포배양기중TNF-á화IL-1a적치.결과 연골세포수도불동대소정압력후,작용조기세포조망현저(P<0.05),수시간연장조망치출현불동적변화.PCNA적표체재불동적압력하화대조조비교균유차이유통계학의의(P<0.05).TNF-á가중복쌍인소분석,시간화압력적교호작용(F=6.90,P<0.01).IL-1a가중복쌍인소분석,시간화압력적교호작용(F=5.80,P<0.01).결론 연골세포재지속고압력응력하조망증가,증식감소;재지속저압력시출현상반적결과 .연골세포적조망화증식화TNF-á화IL-1a변화유일정적상관성.
Objective To investigate the effects of static pressure on apoptosis and proliferation of condrocytes and the correlation between IL-1β and TNF-α and the apoptosis of ehondroeytes. Methods The chondrocytes of rabbits were cultivated in different static pressure conditions (20,40,70 kp) for different durations (0,4,16,24 h) respectively,then the cells were collected. The apoptosis of chondrocytes was assayed by FCM. The expression of PCNA was detected. The IL-113 and TNF-a of culture meditun were evaluated at same time. Results The apoptosis of ehondrocytes was increased after mechanical stimuli whatever its magnitude. With prolongation of time,the apoptosis index had different changes (P < 0.05). The proliferation were inhibited at first 4 hours ( P < 0.05 ), and then inereased rapidly after the following time. TNF-αtwas increased with the time lasting at 40 kp and 70 kp, and it correlated to chondrocyte apoptosis. The IL-1 [3was decreased with the time lasting at 70 kp, and it negative correlated apoptosis of chondrocyte,we also found the IL-1βdecreased when enhanced pressure on 24 h and it correlated the PCNA express at 24 h. Conclusion So we could conclued that the number of chandrocytes were decreased at high static pressure and long effect time.