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利用简易透析培养装置将人诱导多能干细胞分化为确定的内胚层。

Differentiation of Human Induced Pluripotent Stem Cells into Definitive Endoderm Using Simple Dialysis Culture Device.

机构信息

Department of Bioengineering, Graduate School of Engineering, The University of Tokyo, Tokyo, Japan.

Department of Chemical System Engineering, Graduate School of Engineering, The University of Tokyo, Tokyo, Japan.

出版信息

Methods Mol Biol. 2022;2454:731-742. doi: 10.1007/7651_2021_388.

Abstract

Therapeutic use of differentiated organ cells from human induced pluripotent stem cells (hiPSCs) is one of the promising strategies for regenerative medicine. Differentiation into definitive endoderm is an essential process in the preparation of metabolic organs. However, the manufacturability of differentiation is limited due to the high-cost cytokines required for the differentiation of endodermal lineage. Furthermore, the cytokines remaining in the used culture medium and possible endogenous factors are removed along with toxic metabolites by the medium replacement. To address these problems, the application of dialysis culture can retain and fully utilize their accumulation to create a better culture environment that contributes to differentiation cost reduction.

摘要

分化的人诱导多能干细胞(hiPSCs)器官细胞的治疗用途是再生医学的有前途的策略之一。向确定的内胚层分化是代谢器官制备中的一个必要过程。然而,由于分化内胚层谱系所需的高成本细胞因子,分化的可制造性受到限制。此外,通过培养基更换去除留在使用的培养基中的细胞因子和可能的内源性因素以及毒性代谢物。为了解决这些问题,可以应用透析培养来保留和充分利用它们的积累,以创建一个更好的培养环境,有助于降低分化成本。

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