中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
9期
1559-1560
,共2页
任龙韬%卫陈刚%牛建鹏%郭志坚%郝海虎
任龍韜%衛陳剛%牛建鵬%郭誌堅%郝海虎
임룡도%위진강%우건붕%곽지견%학해호
髓核细胞%生物力学%黏弹性
髓覈細胞%生物力學%黏彈性
수핵세포%생물역학%점탄성
Nucleus pulposus cells%Biomechanics%Viscoelastic properties
目的 观察正常髓核细胞的黏弹性。方法 髓核组织取材于3例脊柱侧凸矫形手术者术中取出废弃的髓核组织,用胰蛋白酶和Ⅱ型胶原酶消化分离细胞,Ⅱ型胶原免疫荧光组化和蕃红染色进行细胞鉴定,测量细胞直径,采用微管吸吮技术分析髓核细胞的黏弹性特性。结果 髓核细胞直径为(15.40±1.83)μm,正常髓核细胞的黏弹性参数k1(0.101 ±0.052) kPn、k2(0.353±0.199) kPa和μ(3.034±1.843) kPa·s。直线相关性分析表明,仅k1与髓核细胞直径明显相关(r=-0.389,P<0.05)。结论 正常髓核细胞表现为典型的黏弹性固体蠕变特征;微管吸吮技术可以作为测量髓核细胞生物力学特性的可靠方法。
目的 觀察正常髓覈細胞的黏彈性。方法 髓覈組織取材于3例脊柱側凸矯形手術者術中取齣廢棄的髓覈組織,用胰蛋白酶和Ⅱ型膠原酶消化分離細胞,Ⅱ型膠原免疫熒光組化和蕃紅染色進行細胞鑒定,測量細胞直徑,採用微管吸吮技術分析髓覈細胞的黏彈性特性。結果 髓覈細胞直徑為(15.40±1.83)μm,正常髓覈細胞的黏彈性參數k1(0.101 ±0.052) kPn、k2(0.353±0.199) kPa和μ(3.034±1.843) kPa·s。直線相關性分析錶明,僅k1與髓覈細胞直徑明顯相關(r=-0.389,P<0.05)。結論 正常髓覈細胞錶現為典型的黏彈性固體蠕變特徵;微管吸吮技術可以作為測量髓覈細胞生物力學特性的可靠方法。
목적 관찰정상수핵세포적점탄성。방법 수핵조직취재우3례척주측철교형수술자술중취출폐기적수핵조직,용이단백매화Ⅱ형효원매소화분리세포,Ⅱ형효원면역형광조화화번홍염색진행세포감정,측량세포직경,채용미관흡전기술분석수핵세포적점탄성특성。결과 수핵세포직경위(15.40±1.83)μm,정상수핵세포적점탄성삼수k1(0.101 ±0.052) kPn、k2(0.353±0.199) kPa화μ(3.034±1.843) kPa·s。직선상관성분석표명,부k1여수핵세포직경명현상관(r=-0.389,P<0.05)。결론 정상수핵세포표현위전형적점탄성고체연변특정;미관흡전기술가이작위측량수핵세포생물역학특성적가고방법。
Objective To study the viscoelastic properties of nucleus pulposus (NP) cells from human in vitro. Methods NP was obtained from discarded NP tissue of 3 scoliosis patients aged from 13 to 16 years. Pancreatin and collagenase type Ⅱ were used to digest NP and cells were isolated from NP. Type Ⅱ collagen immunofluorescence and Fan seaing were used to identify NP cells. The micropipette aspiration test was used in combination with a three-parameter viscoelastic solid model to measure the mechanical properties of NP cells. Results The mean diameter of the digested NP cells was ( 15.40 ± 1.83) μm. In response to a prescribed pressure, the NP cells exhibited viscolastic solid creep behavior, which was characterized initially by a jump in displacement followed by a monotony decreasing rate of deformation that generally reached an equilibrium. NP cells were deformed to a length as much as 2 times the radius of the micropipette without completely entering the micropipette. The viscolastic parameters were k1 (0. 101 ±0. 052) kPa, k2 (0. 353 ± 0. 199) kPa, and μ ( 3. 034 ± 1. 843 ) kPa· s, respectively. Only the k1 was positively correlated to the cell diameter (r =-0. 389, P < 0. 05 ). Conclusion Human normal NP cells behave as a typical viscolastic solid creep. Micropipette aspiration technique is a valid method for the study on biomechanics of NP cells.