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仿生培养策略在间充质基质细胞临床扩增中的应用

Biomimetic Culture Strategies for the Clinical Expansion of Mesenchymal Stromal Cells.

机构信息

Charles Perkins Center, The University of Sydney, Sydney, New South Wales 2006, Australia.

School of Life and Environmental Sciences, The University of Sydney, Sydney, New South Wales 2006, Australia.

出版信息

ACS Biomater Sci Eng. 2023 Jul 10;9(7):3742-3759. doi: 10.1021/acsbiomaterials.0c01538. Epub 2021 Feb 18.

DOI:10.1021/acsbiomaterials.0c01538
PMID:33599471
Abstract

Mesenchymal stromal/stem cells (MSCs) typically require significant ex vivo expansion to achieve the high cell numbers required for research and clinical applications. However, conventional MSC culture on planar (2D) plastic surfaces has been shown to induce MSC senescence and decrease cell functionality over long-term proliferation, and usually, it has a high labor requirement, a high usage of reagents, and therefore, a high cost. In this Review, we describe current MSC-based therapeutic strategies and outline the important factors that need to be considered when developing next-generation cell expansion platforms. To retain the functional value of expanded MSCs, ex vivo culture systems should ideally recapitulate the components of the native stem cell microenvironment, which include soluble cues, resident cells, and the extracellular matrix substrate. We review the interplay between these stem cell niche components and their biological roles in governing MSC phenotype and functionality. We discuss current biomimetic strategies of incorporating biochemical and biophysical cues in MSC culture platforms to grow clinically relevant cell numbers while preserving cell potency and stemness. This Review summarizes the current state of MSC expansion technologies and the challenges that still need to be overcome for MSC clinical applications to be feasible and sustainable.

摘要

间充质基质/干细胞 (MSCs) 通常需要大量的体外扩增,才能达到研究和临床应用所需的高细胞数量。然而,在平面(2D)塑料表面上进行常规 MSC 培养已被证明会诱导 MSC 衰老并降低长期增殖过程中的细胞功能,而且通常需要大量的劳动力、试剂的大量使用,因此成本很高。在这篇综述中,我们描述了基于 MSC 的治疗策略,并概述了在开发下一代细胞扩增平台时需要考虑的重要因素。为了保持扩增 MSC 的功能价值,体外培养系统应理想地重现天然干细胞微环境的组成部分,包括可溶性线索、常驻细胞和细胞外基质基质。我们回顾了这些干细胞生态位成分之间的相互作用及其在调控 MSC 表型和功能中的生物学作用。我们讨论了目前在 MSC 培养平台中整合生化和生物物理线索的仿生策略,以在保持细胞效力和干细胞特性的同时培养出具有临床相关性的细胞数量。本综述总结了 MSC 扩增技术的现状以及仍需要克服的挑战,以使 MSC 临床应用具有可行性和可持续性。

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