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. 2023 Apr 18;27:31. doi: 10.1186/s40824-023-00371-0

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© The Author(s) 2023

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Comparative analyses between several types of MSCs. MSC have multiple sources of origin such as bone marrow, adipose tissue, umbilical cord, dental pulp, and peripheral blood. Each source has varying level of accessibility and isolation method. Moreover, depending on the source of MSC, differences in proliferation capacity, differentiation potentials, immunogenicity, and immunoregulation are observed. Comparison was based from the most current studies on MSC.