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Human mesenchymal stem cells inhibit the differentiation and effector functions of monocytes


Citation

Maqbool, Maryam and Algraittee, Satar Jabbar Rahi and Borojerdi, Mohadese Hashem and Sarmadi, Vahid Hosseinpour and John, Cini Mathew and Vidyadaran, Sharmili and Ramasamy, Rajesh (2020) Human mesenchymal stem cells inhibit the differentiation and effector functions of monocytes. Innate Immunity, 26 (5). 424 - 434. ISSN 1753-4259; ESSN: 1753-4267

Abstract

Although monocytes represent an essential part of the host defence system, their accumulation and prolonged stimulation could be detrimental and may aggravate chronic inflammatory diseases. The present study has explored the less-understood immunomodulatory effects of mesenchymal stem cells on monocyte functions. Isolated purified human monocytes were co-cultured with human umbilical cord-derived mesenchymal stem cells under appropriate culture conditions to assess monocytes’ vital functions. Based on the surface marker analysis, mesenchymal stem cells halted monocyte differentiation into dendritic cells and macrophages and reduced their phagocytosis functions, which rendered an inability to stimulate T-cell proliferation. The present study confers that mesenchymal stem cells exerted potent immunosuppressive activity on monocyte functions such as differentiation, phagocytosis and Ag presentation; hence, they promise a potential therapeutic role in down-regulating the unwanted monocyte-mediated immune responses in the context of chronic inflammatory diseases.


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Additional Metadata

Item Type: Article
Divisions: Faculty of Medicine and Health Science
DOI Number: https://doi.org/10.1177/1753425919899132
Publisher: SAGE Publications
Keywords: Mesenchymal stem cells; Monocytes; Phagocytosis; Antigen presentation; Immunosuppression
Depositing User: Ms. Nuraida Ibrahim
Date Deposited: 03 Sep 2021 21:05
Last Modified: 03 Sep 2021 21:05
Altmetrics: http://www.altmetric.com/details.php?domain=psasir.upm.edu.my&doi=10.1177/1753425919899132
URI: http://psasir.upm.edu.my/id/eprint/89220
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