用于临床研究的人脐带间充质干细胞的分离、生物学特征描述和质量检查

Xia Lin Zuo, Dongcheng Wu, Ding Yu, M. A. Sa’ad, Samantha Lo Yin Teng, Manickam Ravichandran, Ke Xiang Ding, Seng Kong Tham
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摘要

背景:人脐带间充质干细胞(hUCMSCs)是从新生儿脐带组织中提取的一种宝贵的多功能细胞类型。这些细胞表现出多种特性,包括多能分化潜能和低免疫原性。hUCMSCs 具有临床应用前景,但其染色体稳定性仍令人担忧。本研究采用短串联重复(STR)分析来评估基因组完整性。通过重点研究染色体稳定性,该研究旨在增强人们对 hUCMSCs 临床生存能力的信心,从而促进其在再生医学中的安全、有效应用。第三代 hUCMSCs 经过了生物学特性鉴定和质量检查,包括细胞形态、活力、生长曲线、表面标记、细胞周期和多系分化潜能检查。本研究结果表明,hUCMSCs 具有间充质干细胞的特征,生长旺盛,存活率高。阳性表面标记表达率超过 95%,而阴性标记表达率低于 2%。细胞核型分析、STR谱鉴定和染色体微阵列分析证实了基因的稳定性。微生物检测表明不存在污染物,免疫学研究则证明了 hUCMSCs 的免疫调节能力。未检测到胰蛋白酶等特定残留物。总之,在严格的 GLP 和 GMP 条件下生产的 hUCMSCs 符合各种干细胞疗法临床应用的质量标准。研究结果支持 hUCMSCs 在各种医疗领域的临床应用。
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Isolation, Biological Characterization, and Quality Inspection of Human Umbilical Cord-derived Mesenchymal Stem Cells for Clinical Research
Background: Human umbilical cord mesenchymal stem cells (hUCMSCs) represent a valuable and versatile cell type derived from the umbilical cord tissue of newborns. These cells exhibit diverse characteristics, including multipotent differentiation potential and low immunogenicity. hUCMSCs hold promise for clinical applications, yet concerns persist regarding their chromosomal stability. This study employs short tandem repeat (STR) analysis to assess genomic integrity. By focusing on chromosomal stability, the study aims to enhance confidence in the clinical viability of hUCMSCs, contributing to their safe and effective use in regenerative medicine. hUCMSCs were extracted from healthy newborn umbilical cords using tissue block adherence and enzyme digestion. The third generation of hUCMSCs undergoes biological characterization and quality checks, including examinations of cell morphology, viability, growth curves, surface markers, cell cycle, and multi-lineage differentiation potential. The result of the present study shows that hUCMSCs exhibit mesenchymal stem cell characteristics, with robust growth and high viability. Positive surface markers are expressed at rates exceeding 95%, while negative markers are ≤2%. Cell karyotyping analysis, STR spectrum identification, and chromosomal microarray analysis confirm genetic stability. Microbial testing shows the absence of contaminants, and immunological studies demonstrate the immunomodulatory capabilities of hUCMSCs. Specific residues, such as trypsin, were not detected. In conclusion, hUCMSCs produced under strict GLP and GMP conditions meet the quality guidelines for clinical application in various stem cell therapies. The findings support the clinical application of hUCMSCs in various medical contexts.
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