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将丝素蛋白微球整合到培养物中对3T3细胞聚集体活力和增殖的维持。

Maintenance of viability and proliferation of 3T3 cell aggregates incorporating fibroin microspheres into cultures.

作者信息

Ryu Da Yeong, Kwon Se Chang, Kim Ji Young, Hur Won

机构信息

Department of Biotechnology and Bioengineering, Kangwon National University, Chuncheon, 200-701, South Korea.

出版信息

Cytotechnology. 2020 Aug;72(4):579-587. doi: 10.1007/s10616-020-00408-5. Epub 2020 Aug 14.

Abstract

This study investigated whether micron-sized microspheres can be used as dispersed scaffolds where anchorage-dependent cells can proliferate and survive in suspension culture. Aggregates of murine 3T3 cells in a non-adherent plate cultured remained viable for more than 2 weeks by the presence of 0.5 mg/ml fibroin microspheres. A nucleoside incorporation assay confirmed the proliferation of 3T3 cells in the aggregates only when cultured with microspheres. Under these conditions, the glucose consumption rate of 3T3 cells increased to 66.5 nmol day cell. Histological analysis demonstrated that the intercellular space of cell aggregates was larger in cultures supplemented with 0.5 mg/ml microspheres than in non-supplemented cultures. The cell aggregates with microspheres also exhibited a reduced arrest in G1 phase. Transmission electron microscopy verified the presence of microspheres in the space between cells in aggregates. Fibroin microspheres maintained the viability and proliferability of 3T3 cells cultured under non-adherent conditions and thus can be used to develop viable suspensions of anchorage-dependent cells.

摘要

本研究调查了微米级微球是否可用作分散支架,使贴壁依赖型细胞能够在悬浮培养中增殖和存活。在非贴壁平板培养中,由于存在0.5mg/ml的丝素蛋白微球,小鼠3T3细胞聚集体可存活超过2周。核苷掺入试验证实,只有在与微球一起培养时,3T3细胞聚集体中的细胞才会增殖。在这些条件下,3T3细胞的葡萄糖消耗率增加到66.5nmol·天·细胞。组织学分析表明,添加0.5mg/ml微球的培养物中细胞聚集体的细胞间隙比未添加微球的培养物中的更大。含有微球的细胞聚集体在G1期的停滞也减少。透射电子显微镜证实了聚集体中细胞间空间存在微球。丝素蛋白微球维持了在非贴壁条件下培养的3T3细胞的活力和增殖能力,因此可用于开发贴壁依赖型细胞的活性悬浮液。

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Efficient formation of cell spheroids using polymer nanofibers.利用聚合物纳米纤维高效形成细胞球。
Biotechnol Lett. 2012 May;34(5):795-803. doi: 10.1007/s10529-011-0836-9. Epub 2011 Dec 30.

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