克隆形成试验
脐带
外周血单个核细胞
男科
低温保存
脐带血
流式细胞术
干细胞
活力测定
间充质干细胞
免疫学
分子生物学
细胞
医学
化学
生物
病理
体外
生物化学
细胞生物学
胚胎
作者
F.G. Pereira-Cunha,Adriana da Silva Santos Duarte,S.C. Reis-Alves,Sara Teresinha Olalla Saad,Konradin Metze,Irene Lorand‐Metze,Ângela Cristina Malheiros Luzo
出处
期刊:Vox Sanguinis
[Wiley]
日期:2014-10-21
卷期号:108 (1): 72-81
被引量:8
摘要
Background and Objectives Umbilical cord blood ( UCB ) is a good stem cell source for cell therapy. We recently demonstrated that cord blood mononuclear cell ( MNC s) subtypes were viable and functional until 96 h after collection, even stored at room temperature. Now, we analyzed the viability and functionality of the cells before and after cryopreservation. Materials and Methods Twenty UCB units were analyzed at 24 and 96 h after collection, frozen for 6 months, thawed and re‐evaluated. MNC s were analyzed by flow cytometry, viability by 7‐ AAD and clonogenic assays ( CFU ) were performed. Results After 96 h of storage, no substantial loss of MNC was found (median 7·320 × 10 6 × 6·305 × 10 6 ). Percentage and viability CD 34 + cells, B‐cell precursors and mesenchymal stem cells were not affected. However, mature B and T lymphocytes as well as granulocytes had a substantial loss. CFU growth was observed in all samples. Prefreezing storage of 96 h was associated with a relative loss of colony formation (median 12%). Postthaw, this loss had a median of 49% (24 h samples) to 56% (96 h samples). Conclusion The delay of 96 h before UCB processing is possible, without a prohibitive impairment of CD 34 + loss in number and functionality.
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