Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.

The immunoregulatory properties of mesenchymal stem cells (MSC) have been demonstrated on a wide range of cells. Here, we describe the modulatory effects of mouse bone marrow-derived MSC on BV2 microglia proliferation rate, nitric oxide (NO) production and CD40 expression. Mouse bone marrow MSC were...

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Main Authors: Ooi, Yin Yin, Ramasamy, Rajesh, Rahmat, Zul'Atfi, Subramaiam, Hemavathy, Tan, Shi Wei, Abdullah, Maha, Ahmad Israf, Daud, Vidyadaran, Sharmili
Format: Article
Published: Elsevier 2010
Online Access:http://psasir.upm.edu.my/id/eprint/13441/
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author Ooi, Yin Yin
Ramasamy, Rajesh
Rahmat, Zul'Atfi
Subramaiam, Hemavathy
Tan, Shi Wei
Abdullah, Maha
Ahmad Israf, Daud
Vidyadaran, Sharmili
author_facet Ooi, Yin Yin
Ramasamy, Rajesh
Rahmat, Zul'Atfi
Subramaiam, Hemavathy
Tan, Shi Wei
Abdullah, Maha
Ahmad Israf, Daud
Vidyadaran, Sharmili
author_sort Ooi, Yin Yin
building UPM Institutional Repository
collection Online Access
description The immunoregulatory properties of mesenchymal stem cells (MSC) have been demonstrated on a wide range of cells. Here, we describe the modulatory effects of mouse bone marrow-derived MSC on BV2 microglia proliferation rate, nitric oxide (NO) production and CD40 expression. Mouse bone marrow MSC were co-cultured with BV2 cells at various seeding density ratios and activated with lipopolysaccharide (LPS). We show that MSC exert an anti-proliferative effect on microglia and are potent producers of NO when stimulated by soluble factors released by LPS-activated BV2. MSC suppressed proliferation of both untreated and LPS-treated microglia in a dose-dependent manner, significantly reducing BV2 proliferation at seeding density ratios of 1:0.2 and 1:0.1 (p < .05). Co-culturing MSC with BV2 cells at different ratios revealed interesting dynamics in NO production. A high number of MSC significantly increases NO in co-cultures whilst a lower number reduces NO. The increased NO levels in co-cultures may be MSC-derived, as we also show that activated BV2 cells stimulate MSC to produce NO. Cell-cell interaction is not a requirement for this effect as soluble factors released by activated BV2 cells alone do stimulate MSC to produce high levels of NO. Although NO is implicated as a mediator for T cell proliferation, it does not appear to play a major role in the suppression of microglia proliferation. Additionally, MSC reduced the expression of the microglial co-stimulator molecule, CD40. Collectively, these regulatory effects of MSC on microglia offer insight into the potential moderating properties of MSC on inflammatory responses within the CNS.
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spelling upm-134412014-11-13T07:44:04Z http://psasir.upm.edu.my/id/eprint/13441/ Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide. Ooi, Yin Yin Ramasamy, Rajesh Rahmat, Zul'Atfi Subramaiam, Hemavathy Tan, Shi Wei Abdullah, Maha Ahmad Israf, Daud Vidyadaran, Sharmili The immunoregulatory properties of mesenchymal stem cells (MSC) have been demonstrated on a wide range of cells. Here, we describe the modulatory effects of mouse bone marrow-derived MSC on BV2 microglia proliferation rate, nitric oxide (NO) production and CD40 expression. Mouse bone marrow MSC were co-cultured with BV2 cells at various seeding density ratios and activated with lipopolysaccharide (LPS). We show that MSC exert an anti-proliferative effect on microglia and are potent producers of NO when stimulated by soluble factors released by LPS-activated BV2. MSC suppressed proliferation of both untreated and LPS-treated microglia in a dose-dependent manner, significantly reducing BV2 proliferation at seeding density ratios of 1:0.2 and 1:0.1 (p < .05). Co-culturing MSC with BV2 cells at different ratios revealed interesting dynamics in NO production. A high number of MSC significantly increases NO in co-cultures whilst a lower number reduces NO. The increased NO levels in co-cultures may be MSC-derived, as we also show that activated BV2 cells stimulate MSC to produce NO. Cell-cell interaction is not a requirement for this effect as soluble factors released by activated BV2 cells alone do stimulate MSC to produce high levels of NO. Although NO is implicated as a mediator for T cell proliferation, it does not appear to play a major role in the suppression of microglia proliferation. Additionally, MSC reduced the expression of the microglial co-stimulator molecule, CD40. Collectively, these regulatory effects of MSC on microglia offer insight into the potential moderating properties of MSC on inflammatory responses within the CNS. Elsevier 2010-12 Article PeerReviewed Ooi, Yin Yin and Ramasamy, Rajesh and Rahmat, Zul'Atfi and Subramaiam, Hemavathy and Tan, Shi Wei and Abdullah, Maha and Ahmad Israf, Daud and Vidyadaran, Sharmili (2010) Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide. International Immunopharmacology, 10 (12). pp. 1532-1540. ISSN 1567-5769; ESSN: 1878-1705 10.1016/j.intimp.2010.09.001
spellingShingle Ooi, Yin Yin
Ramasamy, Rajesh
Rahmat, Zul'Atfi
Subramaiam, Hemavathy
Tan, Shi Wei
Abdullah, Maha
Ahmad Israf, Daud
Vidyadaran, Sharmili
Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title_full Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title_fullStr Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title_full_unstemmed Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title_short Bone marrow-derived mesenchymal stem cells modulate BV2 microglia responses to lipopolysaccharide.
title_sort bone marrow-derived mesenchymal stem cells modulate bv2 microglia responses to lipopolysaccharide.
url http://psasir.upm.edu.my/id/eprint/13441/
http://psasir.upm.edu.my/id/eprint/13441/