Comparative analysis of mesenchymal stem cells cultivated in serum free media

间充质干细胞 干细胞 胎牛血清 免疫原性 生物 细胞生物学 脂肪组织 细胞疗法 细胞培养 免疫学 免疫系统 细胞 生物化学 遗传学
作者
Joo Youn Lee,Min-Hee Kang,Ji Eun Jang,Joon Jeong,Yuyeong Yang,Ji Yong Choi,Hong Seok Kang,Uiil Lee,Ji Woong Choung,Hyeryeon Jung,Young‐Chan Yoon,Kyung Hee Jung,Soon‐Sun Hong,Eugene C. Yi,Sang Gyu Park
出处
期刊:Scientific Reports [Nature Portfolio]
卷期号:12 (1) 被引量:25
标识
DOI:10.1038/s41598-022-12467-z
摘要

Stem cells are attractive candidates for the regeneration of tissue and organ. Mesenchymal stem cells (MSCs) have been extensively investigated for their potential applications in regenerative medicine and cell therapy. For developing effective stem cell therapy, the mass production of consistent quality cells is required. The cell culture medium is the most critical aspect of the mass production of qualified stem cells. Classically, fetal bovine serum (FBS) has been used as a culture supplement for MSCs. Due to the undefined and heterologous composition of animal origin components in FBS, efforts to replace animal-derived components with non-animal-derived substances led to safe serum free media (SFM). Adipose derived mesenchymal stem cells (ADSCs) cultivated in SFM provided a more stable population doubling time (PDT) to later passage and more cells in a shorter time compared to FBS containing media. ADSCs cultivated in SFM had lower cellular senescence, lower immunogenicity, and higher genetic stability than ADSCs cultivated in FBS containing media. Differential expression analysis of mRNAs and proteins showed that the expression of genes related with apoptosis, immune response, and inflammatory response were significantly up-regulated in ADSCs cultivated in FBS containing media. ADSCs cultivated in SFM showed similar therapeutic efficacy in an acute pancreatitis mouse model to ADSCs cultivated in FBS containing media. Consideration of clinical trials, not only pre-clinical trial, suggests that cultivation of MSCs using SFM might offer more safe cell therapeutics as well as repeated administration due to low immunogenicity.
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