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在无动物成分的定义条件下,培养基、基质和外源性因素对人多能干细胞的黏附和生长的协同作用。

Synergistic effect of medium, matrix, and exogenous factors on the adhesion and growth of human pluripotent stem cells under defined, xeno-free conditions.

机构信息

Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

Stem Cells Dev. 2012 Jul 20;21(11):2036-48. doi: 10.1089/scd.2011.0489. Epub 2012 Jan 26.

Abstract

Human pluripotent stem cells (hPSCs), including human embryonic stem cells (hESCs) and human induced pluripotent stem cells (hiPSCs), share the properties of unlimited self-renewal and the capacity to become any cell type in the body, making them well suited for regenerative medicine and cell therapy. So far, almost all hPSC lines have been directly or indirectly exposed to animal-derived products, which would hinder their use for clinical purposes. One of the biggest challenges in this area is to remove animal components from the derivation, propagation, and cryopreservation of hPSCs. Moreover, the presence of undefined components of animal or human origin in culture system may interfere with the interpretation of the effect of exogenous agents on the growth and differentiation of hPSCs and are prone to significant variability. To explore hPSC expansion in defined, xeno-free conditions, 2 different groups of culture systems were used to culture different hESC and hiPSC lines. Our results suggested that (1) medium, matrix, and exogenous factors have synergistic effects on the adhesion and growth of hPSCs; (2) cooperation of exogenous factors including basic fibroblast growth factor, Rho-associated kinase inhibitor (ROCK), and other growth factors is critical for hPSC adhesion and proliferation; (3) basal media have different effects on hPSC attachment to the culture surface; and (4) a medium or matrix component can work synergistically in one culture system, and not at all in another. In this study, we found that Vitronectin/TeSR2 and PDL/HEScGRO (Y-27632) systems were optimal for maintaining the long-term culture of 3 hESC lines and 2 hiPSC lines under defined, xeno-free conditions.

摘要

人类多能干细胞(hPSCs),包括人类胚胎干细胞(hESCs)和人类诱导多能干细胞(hiPSCs),具有无限自我更新和成为体内任何细胞类型的能力,非常适合再生医学和细胞治疗。到目前为止,几乎所有的 hPSC 系都直接或间接接触过动物源性产品,这将阻碍它们用于临床目的。该领域的最大挑战之一是从 hPSCs 的衍生、增殖和冷冻保存中去除动物成分。此外,培养体系中动物或人源性的未知成分的存在可能会干扰外源性物质对 hPSCs 生长和分化的影响的解释,并容易产生显著的可变性。为了在无定义、无动物成分的条件下探索 hPSC 的扩增,使用了 2 种不同的培养体系来培养不同的 hESC 和 hiPSC 系。我们的结果表明:(1)培养基、基质和外源性因素对 hPSC 的黏附和生长具有协同作用;(2)碱性成纤维细胞生长因子、Rho 相关激酶抑制剂(ROCK)和其他生长因子等外源性因素的协同作用对 hPSC 的黏附和增殖至关重要;(3)基础培养基对 hPSC 附着到培养表面有不同的影响;(4)一种培养基或基质成分在一种培养体系中可以协同作用,而在另一种培养体系中则完全没有作用。在这项研究中,我们发现 Vitronectin/TeSR2 和 PDL/HEScGRO(Y-27632)系统在无定义、无动物成分的条件下,是维持 3 种 hESC 系和 2 种 hiPSC 系长期培养的最佳选择。

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