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 Jan 20;24(3):2085.
doi: 10.3390/ijms24032085.

Mesenchymal Stem Cells and Their Exocytotic Vesicles

Affiliations
Review

Mesenchymal Stem Cells and Their Exocytotic Vesicles

Hao Cai et al. Int J Mol Sci. .

Abstract

Mesenchymal stem cells (MSCs), as a kind of pluripotent stem cells, have attracted much attention in orthopedic diseases, geriatric diseases, metabolic diseases, and sports functions due to their osteogenic potential, chondrogenic differentiation ability, and adipocyte differentiation. Anti-inflammation, anti-fibrosis, angiogenesis promotion, neurogenesis, immune regulation, and secreted growth factors, proteases, hormones, cytokines, and chemokines of MSCs have been widely studied in liver and kidney diseases, cardiovascular and cerebrovascular diseases. In recent years, many studies have shown that the extracellular vesicles of MSCs have similar functions to MSCs transplantation in all the above aspects. Here we review the research progress of MSCs and their exocrine vesicles in recent years.

Keywords: cardiocerebral diseases; differentiation; extracellular vesicles; immunomodulation; mesenchymal stem cells; signaling pathways.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

Figure 1
Figure 1
Effects and regulation of MSCs and their exocytotic vesicles in different systems. All solid black lines indicate association or signaling pathways at both ends, solid lines of each color with arrows indicate a promoting relationship, solid lines of each color with horizontal bars represent an inhibiting relationship, solid red lines represent angiogenesis promoting (arrows) or inhibiting (horizontal bars) relationships, solid green lines represent proliferation or apoptosis relationships, blue represents neurogenesis, neuronal proliferation or related inhibition, orange represents promotion or inhibition of differentiation, brown represents promotion or inhibition of inflammatory responses, and cyan represents promotion or inhibition of fibrosis.

References

    1. Johnson K., Zhu S., Tremblay M.S., Payette J.N., Wang J., Bouchez L.C., Meeusen S., Althage A., Cho C.Y., Wu X., et al. A stem cell-based approach to cartilage repair. Science. 2012;336:717–721. doi: 10.1126/science.1215157. - DOI - PubMed
    1. Salem H.K., Thiemermann C. Mesenchymal stromal cells: Current understanding and clinical status. Stem Cells. 2010;28:585–596. doi: 10.1002/stem.269. - DOI - PMC - PubMed
    1. Turajane T., Chaveewanakorn U., Fongsarun W., Aojanepong J., Papadopoulos K.I. Avoidance of Total Knee Arthroplasty in Early Osteoarthritis of the Knee with Intra-Articular Implantation of Autologous Activated Peripheral Blood Stem Cells versus Hyaluronic Acid: A Randomized Controlled Trial with Differential Effects of Growth Factor Addition. Stem Cells Int. 2017;2017:8925132. - PMC - PubMed
    1. Wu X., Wang W., Meng C., Yang S., Duan D., Xu W., Liu X., Tang M., Wang H. Regulation of differentiation in trabecular bone-derived mesenchymal stem cells by T cell activation and inflammation. Oncol. Rep. 2013;30:2211–2219. doi: 10.3892/or.2013.2687. - DOI - PubMed
    1. Neybecker P., Henrionnet C., Pape E., Mainard D., Galois L., Loeuille D., Gillet P., Pinzano A. In vitro and in vivo potentialities for cartilage repair from human advanced knee osteoarthritis synovial fluid-derived mesenchymal stem cells. Stem Cell Res. Ther. 2018;9:329. doi: 10.1186/s13287-018-1071-2. - DOI - PMC - PubMed

MeSH terms

LinkOut - more resources