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
. 2018 Aug;14(4):484-499.
doi: 10.1007/s12015-018-9817-x.

Mesenchymal Stem Cells on Horizon: A New Arsenal of Therapeutic Agents

Affiliations
Review

Mesenchymal Stem Cells on Horizon: A New Arsenal of Therapeutic Agents

Zahra Abbasi-Malati et al. Stem Cell Rev Rep. 2018 Aug.

Abstract

Over 10 years, mesenchymal stem cells (MSCs) have been considered as valuable and suitable cells for cell-based therapy applications, particularly in clinical trials. In any case, they are as yet not utilized routinely in clinics. At first, it was believed that MSCs play their roles, especially in regenerative medicine due to their differentiation and cell replacement properties. Interestingly, it is well-known that MSCs mainly exert their therapeutic effects through their vast bioactive factors. These findings turned scientists' consideration toward cell-free therapy concepts. From this point of view, MSCs can be considered as an arsenal of natural bioreactors in variety of therapeutic agents. MSCs inherently express various important therapeutic agents such as growth factors and cytokines that can be manufactured, handled and stored as a prepared-to-go biologic product. In this review, we provide a vision, highlight as well as discuss in order to introduce competitive natural robust bioreactor MSCs on the horizon.

Keywords: Cell-free therapy; Condition medium; MSC; Secretome; Therapeutic agents.

PubMed Disclaimer

References

    1. Implant Dent. 2017 Aug;26(4):607-612 - PubMed
    1. Stem Cells Transl Med. 2015 May;4(5):513-22 - PubMed
    1. Surg Clin North Am. 1997 Jun;77(3):575-86 - PubMed
    1. PLoS One. 2009 May 21;4(5):e5643 - PubMed
    1. Ann Pediatr Endocrinol Metab. 2015 Mar;20(1):8-12 - PubMed

Publication types

MeSH terms

Substances

LinkOut - more resources