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搅拌速率对人骨髓间充质干细胞微载体培养珠对珠传代培养过程中聚集的影响。

Effects of agitation rate on aggregation during beads-to-beads subcultivation of microcarrier culture of human mesenchymal stem cells.

作者信息

Takahashi Iori, Sato Keigo, Mera Hisashi, Wakitani Shigeyuki, Takagi Mutsumi

机构信息

Division of Biotechnology and Macromolecular Chemistry, Graduate School of Engineering, Hokkaido University, Kita-ku, N13W8, Sapporo, 060-8628, Japan.

School of Health and Sports Sciences, Mukogawa Women's University, 6-46 Ikebiraki, Nishinomiya, Hyogo, 663-8558, Japan.

出版信息

Cytotechnology. 2017 Jun;69(3):503-509. doi: 10.1007/s10616-016-9999-5. Epub 2016 Jun 28.

Abstract

With the aim to utilize human mesenchymal stem cells (hMSCs) grown in large scale for regenerative medicine, effects of agitation rate on aggregation during beads-to-beads subcultivation of microcarrier culture of hMSCs were studied. hMSCs could attach and grew on surface-type microcarriers of Cytodex 1, whereas almost no cell elongation and growth were observed on porous type microcarriers of Cytopores. The percentages of aggregated Cytodex 1 microcarriers at an agitation rate of 60 and 90 rpm were lower than that at 30 rpm, which was the lowest agitation rate necessary for the suspension of Cytodex 1 microcarriers, and the cells grew fastest at 60 rpm. hMSC could be subcultivated on Cytodex 1 by the beads-to-beads method at both 30 and 60 rpm without trypsinization. However, agitation at 60 rpm resulted in a markedly lower percentage of aggregated microcarriers not only before but also after subcultivation. The percentages of CD90- and CD166-positive cells among cells grown on Cytodex 1 at 60 rpm (91.5 and 87.6 %) were comparable to those of cells grown in the pre-culture on dishes. In conclusion, hMSCs could be subcultivated on Cytodex 1 by beads-to-beads method maintaining the expressions of the cell surface antigens CD90 and CD166, while adjusting agitation rate could decrease the microcarrier aggregation.

摘要

为了将大规模培养的人间充质干细胞(hMSCs)用于再生医学,研究了搅拌速率对hMSCs微载体培养中珠对珠传代培养过程中聚集的影响。hMSCs可以附着并生长在Cytodex 1表面型微载体上,而在Cytopores多孔型微载体上几乎未观察到细胞伸长和生长。在60和90 rpm搅拌速率下,聚集的Cytodex 1微载体的百分比低于30 rpm时的百分比,30 rpm是悬浮Cytodex 1微载体所需的最低搅拌速率,细胞在60 rpm时生长最快。hMSC可以在30和60 rpm下通过珠对珠法在Cytodex 1上进行传代培养,无需胰蛋白酶消化。然而,60 rpm的搅拌不仅在传代培养前而且在传代培养后都导致聚集微载体的百分比明显降低。在60 rpm下在Cytodex 1上生长的细胞中CD90和CD166阳性细胞的百分比(91.5%和87.6%)与在培养皿中预培养的细胞相当。总之,hMSCs可以通过珠对珠法在Cytodex 1上传代培养,同时保持细胞表面抗原CD90和CD166的表达,而调节搅拌速率可以减少微载体聚集。

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