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生长因子组合培养扩增的人软骨细胞的生物安全性评估:一项临床前研究。

Biosafety evaluation of culture-expanded human chondrocytes with growth factor cocktail: a preclinical study.

作者信息

Al-Masawa Maimonah-Eissa, Wan Kamarul Zaman Wan Safwani, Chua Kien-Hui

机构信息

Department of Physiology, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latiff, Bandar Tun Razak, Cheras, 56000, Kuala Lumpur, Malaysia.

Department of Biomedical Engineering, Faculty of Engineering, University of Malaya, 50603, Kuala Lumpur, Malaysia.

出版信息

Sci Rep. 2020 Dec 9;10(1):21583. doi: 10.1038/s41598-020-78395-y.

Abstract

The scarcity of chondrocytes is a major challenge for cartilage tissue engineering. Monolayer expansion is necessary to amplify the limited number of chondrocytes needed for clinical application. Growth factors are often added to improve monolayer culture conditions, promoting proliferation, and enhancing chondrogenesis. Limited knowledge on the biosafety of the cell products manipulated with growth factors in culture has driven this study to evaluate the impact of growth factor cocktail supplements in chondrocyte culture medium on chondrocyte genetic stability and tumorigenicity. The growth factors were basic fibroblast growth factor (b-FGF), transforming growth factor β2 (TGF β2), insulin-like growth factor 1 (IGF-1), insulin-transferrin-selenium (ITS), and platelet-derived growth factor (PD-GF). Nasal septal chondrocytes cultured in growth factor cocktail exhibited a significantly high proliferative capacity. Comet assay revealed no significant DNA damage. Flow cytometry showed chondrocytes were mostly at G0-G1 phase, exhibiting normal cell cycle profile with no aneuploidy. We observed a decreased tumour suppressor genes' expression (p53, p21, pRB) and no TP53 mutations or tumour formation after 6 months of implantation in nude mice. Our data suggest growth factor cocktail has a low risk of inducing genotoxic and tumorigenic effects on chondrocytes up to passage 6 with 16.6 population doublings. This preclinical tumorigenicity and genetic instability evaluation is crucial for further clinical works.

摘要

软骨细胞的稀缺是软骨组织工程面临的一项重大挑战。单层扩增对于扩大临床应用所需的有限数量软骨细胞至关重要。通常会添加生长因子以改善单层培养条件,促进增殖并增强软骨形成。由于对培养中用生长因子处理的细胞产物的生物安全性了解有限,本研究旨在评估软骨细胞培养基中生长因子鸡尾酒补充剂对软骨细胞遗传稳定性和致瘤性的影响。这些生长因子包括碱性成纤维细胞生长因子(b-FGF)、转化生长因子β2(TGF β2)、胰岛素样生长因子1(IGF-1)、胰岛素-转铁蛋白-硒(ITS)和血小板衍生生长因子(PD-GF)。在生长因子鸡尾酒中培养的鼻中隔软骨细胞表现出显著较高的增殖能力。彗星试验显示无明显的DNA损伤。流式细胞术表明软骨细胞大多处于G0-G1期,呈现正常的细胞周期分布且无非整倍体。我们观察到肿瘤抑制基因(p53、p21、pRB)的表达降低,并且在裸鼠植入6个月后未出现TP53突变或肿瘤形成。我们的数据表明,生长因子鸡尾酒对传代6次、群体倍增次数达16.6的软骨细胞诱导遗传毒性和致瘤性影响的风险较低。这种临床前的致瘤性和遗传不稳定性评估对于进一步的临床工作至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7503/7725787/dd06a72c9240/41598_2020_78395_Fig1_HTML.jpg

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