结论紫外线可诱导软骨细胞凋亡。
Conclusion Ultraviolet radiation could induce apoptosis of chondrocytes.
目的研究骺板软骨细胞冻存的方法。
Objective To study frozen reservation method of epiphyseal plate chondrocyte.
目的:探讨凋亡在软骨细胞分化中的作用。
Objective to explore the effect of apoptosis on chondrocyte differentiation.
可是有很小一部分能形成软骨细胞形成软骨。
A few, though, can produce chondrocytes, the cells that make cartilage.
体外培养观察软骨细胞贴壁和生长均较缓慢。
The in vitro observation showed that cell adherence and growth was slow.
结论转化软骨细胞的生长速度要高于正常软骨细胞。
Conclusions The proliferate rate of transformed chondrocytes is higher than that of normal chondrocytes.
随着胶原层变厚,原来的胶原钙和关节软骨细胞退化。
As the collagen layer thickens, older collagen calcifies and older chondrocytes deteriorate.
方法分离1月龄兔软骨细胞,经离心管内培养形成软骨。
Method Chondrocytes isolated from rabbits aged 1month formed cartilages after cultivation in centrifuge tubes.
结论神经肽对软骨细胞成熟及向骨细胞转化有一定影响。
Conclusion Neuropeptide can influence the mature of chondrocytes and their differentiation into osteocytes.
目的:探讨X线平片在成软骨细胞瘤诊断中的临床价值。
Objective: to evaluate the diagnostic value of chondroblastoma with X-ray plain film.
具有软骨细胞表型特征的永生化兔髁突软骨细胞系的建立。
Establishment of an immortalized chondrocyte cell line with chondrocyte phenotype derived from rabbit mandibular condyle.
结论:正弦波的振动负荷可以影响培养关节软骨细胞的代谢。
CONCLUSION: Vibration loading at a sinusoidal waveform can affect the metabolism of cultured articular chondrocytes.
可以认出软骨组织,清晰的间隙中有软骨细胞,但排列不规则。
The tissue is recognizable as cartilage, and there are chondrocytes in clear Spaces, but there is no orderly pattern.
通过查阅文献对体外培养软骨细胞修复关节软骨缺损进行综述。
This paper aimed to review articular cartilage defects repaired with articular chondrocytes cultured in vitro by consulting literatures.
目的比较转化人关节软骨细胞与正常软骨细胞之间的生物特性。
Objective To delineate the biological features between the transformed human articular chondrocytes and normal chond ro-cytes.
本文报告了人胎儿关节软骨细胞和兔关节软骨细胞的体外培养。
In this research embryo articular cartilage cells and rabbit articular cartilage cells were cultivated in vitro.
建立梅花鹿鹿茸软骨细胞的分离培养方法,培养鹿茸软骨细胞。
The methods of isolation and culture sika deer antler chondrocytes were established.
方法分离收集1月龄兔关节软骨细胞,经离心管内培养形成软骨。
Methods Chondrocytes isolated from articular cartilage of 1 month rabbits formed cartilage after cultivation in centrifuge tubes.
目的观察低剂量t - 2毒素对大鼠体外培养软骨细胞的影响。
Objective to investigate the effect of mini-dose T-2 toxin on chondrocytes in vitro.
随着增殖层细胞逐渐向肥大层软骨细胞分化,软骨厚度逐渐增加。
With the development of articular, the proliferation cells differentiated into hypertrophic cells, and the cartilage thickened.
结论:软骨细胞的密度、形态、表型和缝隙连接之间有一定的关系。
CONCLUSION: There are certain relationships among the density, form, phenotype and gap junction in chondrocytes.
目的:探讨同种异体软骨细胞移植修复关节软骨缺损的免疫学变化。
Objective: To investigate the immunological reaction of allogeneic chondrocytes transplantation for the repair of articular cartilage defect.
人鼻中隔软骨细胞为无菌条件下取鼻中隔偏曲手术患者的鼻中隔软骨。
Human nasal septum chondrocytes were the septal cartilage of nose which was derived from operated patients with deflection of nasal septum under sterile condition.
方法:自3周龄兔关节面分离软骨细胞,经离心管培养2周形成软骨。
Methods:Chondrocytes were isolated from joint surfaces of rabbits aged 3 weeks and formed cartilages by cultivation in centrifuge tubes for 2 weeks.
方法:自3周龄兔关节软骨分离软骨细胞,经离心管培养2周形成软骨。
Methods: Chondrocytes were isolated from articular cartilages of 3 week old rabbits and formed cartilages by cultivation in centrifuge tubes for 2 weeks.
方法用酶消化、分离鸡胚关节软骨细胞,体外单层培养,收集细胞培养液。
Methods Chick embryo joint chondrocytes digested and isolated by enzyme were grown monolayer culture in vitro. Chondrocyte culture media was collected.
结果诱导后成纤维细胞细胞形态由梭形向软骨细胞样多角形、多边形转变。
Results After induction , fibroblasts changed their morphology from spindle shape to typical polygon shape of chondrocytes.
结果诱导后成纤维细胞细胞形态由梭形向软骨细胞样多角形、多边形转变。
Results After induction , fibroblasts changed their morphology from spindle shape to typical polygon shape of chondrocytes.
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