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使用Integra CELLine培养系统提高肿瘤细胞培养物中外泌体的产量。

Increased exosome production from tumour cell cultures using the Integra CELLine Culture System.

作者信息

Mitchell J Paul, Court Jacqueline, Mason Malcolm David, Tabi Zsuzsanna, Clayton Aled

机构信息

Department of Oncology & Palliative Medicine, School of Medicine, Cardiff University, Velindre Cancer Centre, Whitchurch, Cardiff, UK.

出版信息

J Immunol Methods. 2008 Jun 1;335(1-2):98-105. doi: 10.1016/j.jim.2008.03.001. Epub 2008 Apr 3.

Abstract

Exosomes are nanometer-sized vesicles, secreted from most cell types, with documented immune-modulatory functions. Exosomes can be purified from cultured cells but to do so effectively, requires maintenance of cells at high density in order to obtain sufficient accumulation of exosomes in the culture medium, prior to purification. Whilst high density cultures can be achieved with cells in suspension, this remains difficult with adherent cells, resulting in low quantity of exosomes for subsequent study. We have used the Integra CELLine culture system, originally designed for hybridoma cultures, to achieve a significant increase in obtainable exosomes from adherent and non-adherent tumour cells. Traditional cultures of mesothelioma cells (cultured in 75 cm(2) flasks) gave an average yield of 0.78 microg+/-0.14 microg exosome/ml of conditioned medium. The CELLine Adhere 1000 (CLAD1000) flask, housing the same cell line, increased exosome yield approximately 12 fold to 10.06 microg+/-0.97 microg/ml. The morphology, phenotype and immune function of these exosomes were compared, and found to be identical in all respects. Similarly an 8 fold increase in exosome production was obtained from NKL cells (a suspension cell line) using a CELLine 1000 (CL1000) flask. The CELLine system also incurred ~5.5 fold less cost and reduced labour for cell maintenance. This simple culture system is a cost effective, useful method for significantly increasing the quantity of exosomes available from cultured cells, without detrimental effects. This tool should prove advantageous in future studies of exosome-immune modulation in cancer and other settings.

摘要

外泌体是纳米级的囊泡,由大多数细胞类型分泌,具有已被记录的免疫调节功能。外泌体可以从培养的细胞中纯化出来,但要有效做到这一点,需要将细胞维持在高密度状态,以便在纯化之前使外泌体在培养基中充分积累。虽然悬浮细胞可以实现高密度培养,但贴壁细胞仍难以做到,这导致后续研究可用的外泌体数量较少。我们使用了最初设计用于杂交瘤培养的Integra CELLine培养系统,以显著增加从贴壁和非贴壁肿瘤细胞中可获得的外泌体数量。间皮瘤细胞的传统培养(在75 cm²培养瓶中培养)每毫升条件培养基中外泌体的平均产量为0.78微克±0.14微克。容纳相同细胞系的CELLine Adhere 1000(CLAD1000)培养瓶将外泌体产量提高了约12倍,达到10.06微克±0.97微克/毫升。对这些外泌体的形态、表型和免疫功能进行了比较,发现它们在所有方面都相同。同样,使用CELLine 1000(CL1000)培养瓶,NKL细胞(一种悬浮细胞系)的外泌体产量提高了8倍。CELLine系统在细胞维持方面的成本也降低了约5.5倍,并且减少了劳动力。这种简单的培养系统是一种经济高效、有用的方法,可显著增加从培养细胞中获得的外泌体数量,且无有害影响。在未来癌症及其他环境中外泌体免疫调节的研究中,这个工具应会证明是有利的。

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