Title
Immunomodulatory and immunogenic properties of mesenchymal stem cells derived from bovine fetal bone marrow and adipose tissue
Date Issued
01 June 2019
Access level
metadata only access
Resource Type
journal article
Author(s)
University of Chile
Publisher(s)
Elsevier B.V.
Abstract
Little information is currently available on therapeutic features of bovine mesenchymal stem cells (MSCs), despite the development of large animal experimental models including cattle may open alternative strategies for investigating MSC physiology and eventual applications for regenerative therapy. The aim of the present study was to compare in vitro immunomodulatory and immunogenic potentials of bovine fetal MSCs (bfMSCs) derived from bovine fetal bone marrow (BM-MSCs) and adipose tissue (AT-MSCs). Immunomodulatory analyses in bfMSCs were performed by determination of the effect of interferon-γ (IFNγ) on mRNA levels of indoleamine 2, 3-dioxygenase (IDO), transforming growth factor β1 (TGFβ1), prostaglandin E receptor 2 (PTGER2), interleukin-6 and -10 (IL-6 and IL-10), and IDO enzymatic activity. The effect of conditioned medium from IFNγ-stimulated bfMSCs on the proliferation of alloantigen-activated peripheral blood lymphocytes (PBLs) was assessed. Immunogenicity of bfMSCs was determined by quantification of mRNA levels of major histocompatibility complex I and II (MHC-I and -II), CD80 and CD86, and the proportion of cells positive for MHC-I and -II by flowcytometry (FACS) analyses. IFNγ treatment increased IL-6, PTGER2 and IDO gene expression and activity in bfMSCs but did not affect suppressive effect on proliferation of PBLs. Lower proportion of AT-MSCs expressed MHC-I and MHC-II in comparison to BM-MSCs. In conclusion, BM-MSCs and AT-MSCs upregulated expression of immunomodulatory genes in a similar way after IFNγ stimuli. BM-MSCs and AT-MSCs in basal condition and treated with IFNγ displayed similar in vitro immunomodulatory ability. Lower expression of MHC-I and MHC-II suggest that AT-MSCs might be less immunogenic compared to BM-MSCs.
Start page
212
End page
222
Volume
124
Language
English
OCDE Knowledge area
Ciencia veterinaria
Biología celular, Microbiología
Scopus EID
2-s2.0-85063343619
PubMed ID
Source
Research in Veterinary Science
ISSN of the container
00345288
Sponsor(s)
This study was supported by grant ID15I10129 from the Scientific and Technological Development Support Fund (FONDEF) from the Ministry of Education, Government of Chile. The scholarship of Dr. Olger Huaman was funded by the National Program for Scholarships (PRONABEC) from the Government of Perú. We acknowledge Professor Alejandro Escobar from the Faculty of Dentistry of University of Chile for their technical assistance.
Sources of information:
Directorio de Producción Científica
Scopus