[Effects of hydrostatic pressure on proliferation and expression of the differentiated phenotype of cultured chondrocytes derived from rabbit craniofacial complex].

S Soma
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Abstract

To investigate the effects of mechanical forces on the growth of cartilages of the craniofacial complex, chondrocytes isolated from nasal septal cartilage (NSC), spheno-occipital synchondrosis (SOS), and mandibular condylar cartilage (MCC) were cultured and exposed to hydrostatic pressure in vitro. Following results were obtained. 1. By application of the pressure, DNA synthesis increased in NSC and SOS (150% of control by 50 g/cm2, 1 min), but not so much in MCC in the medium containing 10% fetal calf serum (FCS). On the other hand, GAG synthesis increased in SOS (140% of control by 50 g/cm2, 2 min.) and MCC (160% of control by 100 g/cm2, 5 min), but decreased slightly in NSC in the same condition. The stimulations in DNA and GAG syntheses reached maxima 20-22 hr and 24-27 hr respectively after the application of the pressure. These stimulatory effects of the hydrostatic pressure on DNA and GAG syntheses could be found when cultured chondrocytes were in a multilayer stage. 2. It has been reported that addition of FCS at a concentration of 10% increases DNA synthesis in these chondrocytes preincubated in medium containing 0.3% FCS. The application of the pressure 2 min before the addition of 10% FCS potentiated the increase by FCS of DNA synthesis in NSC (130% of control), but not so much that in SOS and little that in MCC. 3. When the pressure was applied on these cells 2 min before addition of parathyroid hormone (PTH; 10(-7) M), this mechanical stimulation potentiated the increase by PTH of GAG synthesis in MCC (130% of control), but not so much that in SOS, and little that in NSC. Moreover, the intracellular cAMP level which was increased just after the addition of PTH also became higher by the application of the pressure. 4. These potentiation by the hydrostatic pressure in the cases of the addition of FCS and PTH diminished when intervals between application of pressure and addition of these factors were more than 10 min. These findings suggested that mechanical forces have influences on the growth of cartilages in craniofacial complex and that these effects are mediated by factors contained in serum.

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[静水压对兔颅面复合体软骨细胞增殖及分化表型表达的影响]。
为了研究机械力对颅面复合体软骨生长的影响,我们从鼻中隔软骨(NSC)、蝶骨-枕软骨联合(SOS)和下颌髁软骨(MCC)中分离软骨细胞进行体外培养和静水压力处理。得到以下结果:1. 通过施加压力,NSC和SOS的DNA合成增加(50 g/cm2, 1 min)为对照的150%,但MCC在含有10%胎牛血清(FCS)的培养基中没有这么多。另一方面,在相同条件下,SOS (50 g/cm2, 2 min)和MCC (100 g/cm2, 5 min, 160%)的GAG合成增加,而NSC的GAG合成略有下降。施加压力后,DNA和GAG合成的刺激分别在20-22小时和24-27小时达到最大。静水压力对DNA和GAG合成的刺激作用可在培养软骨细胞处于多层阶段时发现。2. 据报道,在含有0.3% FCS的培养基中预先培养的软骨细胞中,添加10%浓度的FCS可增加DNA合成。在加入10% FCS前2分钟施加压力,可使NSC的DNA合成增加(为对照的130%),但没有SOS的多,MCC的少。3.在加入甲状旁腺激素(PTH)前2分钟对这些细胞施加压力;10(-7) M),这种机械刺激增强了MCC中PTH对GAG合成的增加(对照组的130%),但没有SOS的那么多,NSC的也很少。此外,在施加压力后,刚加入甲状旁腺激素后升高的细胞内cAMP水平也升高。4. 在添加FCS和PTH的情况下,当施加压力和添加这些因素的时间间隔超过10分钟时,这些由静水压力引起的增强作用就会减弱。这些发现表明,机械力对颅面复合物中软骨的生长有影响,而这些影响是由血清中含有的因素介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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