Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Jun 10:2023:4547875.
doi: 10.1155/2023/4547875. eCollection 2023.

Comparison of Biological Properties and Clinical Application of Mesenchymal Stem Cells from the Mesoderm and Ectoderm

Affiliations
Review

Comparison of Biological Properties and Clinical Application of Mesenchymal Stem Cells from the Mesoderm and Ectoderm

Zhenning Wang et al. Stem Cells Int. .

Abstract

Since the discovery of mesenchymal stem cells (MSCs) in the 1970s, they have been widely used in the treatment of a variety of diseases because of their wide sources, strong differentiation potential, rapid expansion in vitro, low immunogenicity, and so on. At present, most of the related research is on mesoderm-derived MSCs (M-MSCs) such as bone marrow MSCs and adipose-derived MSCs. As a type of MSC, ectoderm-derived MSCs (E-MSCs) have a stronger potential for self-renewal, multidirectional differentiation, and immunomodulation and have more advantages than M-MSCs in some specific conditions. This paper analyzes the relevant research development of E-MSCs compared with that of M-MSCs; summarizes the extraction, discrimination and culture, biological characteristics, and clinical application of E-MSCs; and discusses the application prospects of E-MSCs. This summary provides a theoretical basis for the better application of MSCs from both ectoderm and mesoderm in the future.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Sources and markers of some representative E-MSCs (DPSC-dental pulp stem cells, SCAP-apical dental papilla stem cells, SHED-deciduous dental pulp stem cells, PDLSC-periodontal ligament stem cells, GMSC-gingival mesenchymal stem cells, and JMMSC-jaw marrow-derived mesenchymal stem cells. Red indicates positively expressed while blue indicates negatively expressed surface markers).
Figure 2
Figure 2
Typical extraction process of DPSCs of human.

Similar articles

Cited by

References

    1. Leucht P., Kim J. B., Amasha R., James A. W., Girod S., Helms J. A. Embryonic origin and Hox status determine progenitor cell fate during adult bone regeneration. Development . 2008;135(17):2845–2854. doi: 10.1242/dev.023788. - DOI - PubMed
    1. Lloyd B., Tee B. C., Headley C., Emam H., Mallery S., Sun Z. Similarities and differences between porcine mandibular and limb bone marrow mesenchymal stem cells. Archives of Oral Biology . 2017;77:1–11. doi: 10.1016/j.archoralbio.2017.01.012. - DOI - PMC - PubMed
    1. Erices A., Conget P., Minguell J. J. Mesenchymal progenitor cells in human umbilical cord blood. British Journal of Haematology . 2015;109(1):235–242. doi: 10.1046/j.1365-2141.2000.01986.x. - DOI - PubMed
    1. Bari C. D., Dell'Accio F., Tylzanowski P., Luyten F. P. Multipotent mesenchymal stem cells from adult human synovial membrane. Arthritis & Rheumatology . 2001;44(8):1928–1942. doi: 10.1002/1529-0131(200108)44:8<1928::AID-ART331>3.0.CO;2-P. - DOI - PubMed
    1. Zuk P. A., Zhu M., Mizuno H., et al. Multilineage cells from human adipose tissue: implications for cell-based therapies. Tissue Engineering Part A . 2001;7(2):211–228. doi: 10.1089/107632701300062859. - DOI - PubMed