Premature cellular senescence in isolated chondrocytes from polydactyl cartilage in FBS containing serum in comparison to human serum

H. Shafaei, Azam Farani, Zahra Baghaei, F. Mortazavi
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Abstract

Background. Transplantation of chondrocytes is one of the methods for treatment of articular cartilage defects. For this purpose, it is necessary to isolate these chondrocytes and expand in serum containing culture medium. Sera contain growth factors that are added to medium. Fetal bovine serum (FBS) is used for standard cell culture. However bovine proteins of FBS are accompanied with risk of host immune system reactions. Therefore, it is necessary to replace FBS with human serum for clinical cases. In addition, infants have chondrocytes with high proliferation potency versus adults. In this study, the effects of FBS and human placental serum was investigated on morphology and cellular senescence related genes expression of chondrocytes of infants. Methods. Chondrocytes after isolation of from polydactyly cartilage tissue samples, were cultured in 10% FBS and human serum up to passage 5. Human placental serum was obtained from venous blood of embryonic surface of human placenta. Chondrocytes in two culture medium were compared morphologically by inverted microscope. For cellular senescence evaluation, relative expression of IGF1 and P16 genes were assessed by quantitative real-time RT PCR. Results. Proliferation of chondrocytes is markedly decreased in FBS groups in comparison with human serum. In FBS containing medium, phenotypes of cells were changed from spindle shape to flat appearance after five passages. The expression IGF1 and P16 genes are increased in chondrocytes grown in FBS containing medium and it was significant about P16. Morphologic results were in agreement with Real-time RT PCR results. Conclusion. Human placental serum has advantages such as high proliferation rate on human chondrocytes, prevention from cellular senescence and immunological problems in using cultured chondrocytes for cartilage tissue engineering.
含血清的胎牛血清中多趾软骨分离软骨细胞的过早细胞衰老与人血清的比较
背景。软骨细胞移植是治疗关节软骨缺损的方法之一。为此,有必要分离这些软骨细胞并在含培养基的血清中扩增。血清中含有添加到培养基中的生长因子。胎牛血清(FBS)用于标准细胞培养。然而,牛胎牛蛋白伴宿主免疫系统反应的危险。因此,临床病例有必要用人血清代替胎牛血清。此外,与成人相比,婴儿的软骨细胞具有较高的增殖能力。本研究研究了胎牛血清和人胎盘血清对婴儿软骨细胞形态和细胞衰老相关基因表达的影响。方法。从多指软骨组织样本中分离出软骨细胞,在10%胎牛血清和人血清中培养至5代。人胎盘血清是从人胎盘胚表面静脉血中提取的。倒置显微镜下比较两种培养基中软骨细胞的形态。采用实时荧光定量RT - PCR技术检测IGF1和P16基因的相对表达量。结果。与人血清相比,胎牛血清组软骨细胞增殖明显减少。在含FBS的培养基中,5代后细胞表型由纺锤形变为扁平状。在含FBS培养基中培养的软骨细胞中,IGF1和P16基因表达增加,其中P16表达显著增加。形态学结果与Real-time RT - PCR结果一致。结论。人胎盘血清具有对人软骨细胞增殖率高、防止细胞衰老和利用培养的软骨细胞进行软骨组织工程的免疫问题等优点。
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