Amino Acid Uptake Limitations During Human Mesenchymal Stem Cell-Based Chondrogenesis

软骨发生 氨基酸 生物化学 软骨 间充质干细胞 缬氨酸 化学 亮氨酸 羟脯氨酸 新陈代谢 细胞外基质 必需氨基酸 细胞生物学 生物 体外 解剖
作者
Yi Zhong,Chao Zhang,Rodrigo A. Somoza,Arnold I. Caplan,Jean F. Welter,Harihara Baskaran
出处
期刊:Tissue Engineering Part A [Mary Ann Liebert]
标识
DOI:10.1089/ten.tea.2024.0032
摘要

A mino acids are the essential building blocks for collagen and proteoglycan, which are the main constituents for cartilage extracellular matrix (ECM). Synthesis of ECM proteins requires the uptake of various essential/nonessential amino acids. Analyzing amino acid metabolism during chondrogenesis can help to relate tissue quality to amino acid metabolism under different conditions. In our study, we studied amino acid uptake/secretion using human mesenchymal stem cell (hMSC)-based aggregate chondrogenesis in a serum-free induction medium with a defined chemical formulation. The initial glucose level and medium-change frequency were varied. Our results showed that essential amino acid uptake increased with time during hMSCs chondrogenesis for all initial glucose levels and medium-change frequencies. Essential amino acid uptake rates were initial glucose-level independent. The DNA-normalized glycosaminoglycans and hydroxyproline content of chondrogenic aggregates correlated with cumulative uptake of leucine, valine, and tryptophan regardless of initial glucose levels and medium-change frequencies. Collectively, our results show that amino acid uptake rates during in vitro chondrogenesis were insufficient to produce a tissue with an ECM content similar to that of human neonatal cartilage or adult cartilage. Furthermore, this deficiency was likely related to the downregulation of some key amino acid transporters in the cells. Such deficiency could be partially improved by increasing the amino acid availability in the chondrogenic medium by changing culture conditions.
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