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Methods to produce induced pluripotent stem cell-derived mesenchymal stem cells: Mesenchymal stem cells from induced pluripotent stem cells

Journal

WORLD JOURNAL OF STEM CELLS
Volume 13, Issue 8, Pages 1094-1111

Publisher

BAISHIDENG PUBLISHING GROUP INC
DOI: 10.4252/wjsc.v13.i8.1094

Keywords

Mesenchymal stem cells; Induced pluripotent stem cells; Mesenchymal stem cells derived from induced pluripotent stem cells; Differentiation methods; Culture components; Mesenchymal stem cell markers

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Mesenchymal stem cells (MSCs) have great potential for cell therapy due to their immunomodulatory effects, but their clinical application is restricted by several factors. Induced pluripotent stem cells (iPSCs) offer a new source to generate MSCs, known as iMSCs, which may overcome technical and biological limitations and ethical concerns regarding human embryonic stem cells. Various differentiation methods for iPSCs into MSCs have been developed to meet clinical demands.
Mesenchymal stem cells (MSCs) have received significant attention in recent years due to their large potential for cell therapy. Indeed, they secrete a wide variety of immunomodulatory factors of interest for the treatment of immune-related disorders and inflammatory diseases. MSCs can be extracted from multiple tissues of the human body. However, several factors may restrict their use for clinical applications: the requirement of invasive procedures for their isolation, their limited numbers, and their heterogeneity according to the tissue of origin or donor. In addition, MSCs often present early signs of replicative senescence limiting their expansion in vitro, and their therapeutic capacity in vivo. Due to the clinical potential of MSCs, a considerable number of methods to differentiate induced pluripotent stem cells (iPSCs) into MSCs have emerged. iPSCs represent a new reliable, unlimited source to generate MSCs (MSCs derived from iPSC, iMSCs) from homogeneous and well-characterized cell lines, which would relieve many of the above mentioned technical and biological limitations. Additionally, the use of iPSCs prevents some of the ethical concerns surrounding the use of human embryonic stem cells. In this review, we analyze the main current protocols used to differentiate human iPSCs into MSCs, which we classify into five different categories: MSC Switch, Embryoid Body Formation, Specific Differentiation, Pathway Inhibitor, and Platelet Lysate. We also evaluate common and method-specific culture components and provide a list of positive and negative markers for MSC characterization. Further guidance on material requirements to produce iMSCs with these methods and on the phenotypic features of the iMSCs obtained is added. The information may help researchers identify protocol options to design and/or refine standardized procedures for large-scale production of iMSCs fitting clinical demands.

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