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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/18864

Title: Mutual interactions between Multipotent Adult Progenitor Cells (Multistem® Cells) and macrophages
Authors: Ravanidis, Stelios
Donders, Raf
Bogie, Jeroen F. J.
Craeye, D.
Gijbels, K.
Pinxteren, J.
Hellings, Niels
Issue Date: 2013
Citation: Regenerative Medicine, 8 (S6), (ART N° OP-064), p. S81-S81
Abstract: Question: Multiple sclerosis (MS) is a chronic, inflammatory, demyelinating disease of the central nervous system (CNS) in which infiltrated macrophages and microglia are thought to be the primary effector cells. Effector mechanisms of activated macrophages and microglia include the phagocytosis of myelin, secretion of inflammatory and toxic mediators, such as reactive oxygen and nitrogen species, which affect axonal and myelin integrity. Therapeutic strategies to modulate myeloid cell mediated neuroinflammation are currently explored. Among other approaches stem cell based strategies are under investigation. Multistem® (rMS) is a clinical product of cells isolated under Multipotent Adult Progenitor Cells (MAPCs) culture conditions. So far MAPCs and rMS cells have been used in several experimental approaches such as experimental stroke, traumatic brain injury and several others neuro-inflammatory diseases with promising results. In a model of spinal cord injury it was shown that MAPCs can shift macrophages from a proinflammatory M1 to the anti-inflammatory M2 (alternatively activated) phenotype. Mesenchymal stem cells including rMS seem to be more potent in secreting immunomodulatory molecules such as inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) following licensing with pro-inflammatory cytokines. In this project, we aim to explore the mutual interactions between macrophages and rMS cells in vitro in terms of down regulation of macrophage functions relevant for MS disease promotion. Methods: rMS cells derived from Lewis rat and provided by ReGenesys BVBA (Heverlee, Belgium) were seeded in macrophage medium for 24 hours to obtain conditioned media. rMS were seeded in two different conditions: either 50µl (CM50) or 100 µl (CM100). Serial dilutions of rMS conditioned medium were applied to the rat alveolar macrophage cell line NR8383. In each condition 100 ng/ml LPS was added to induce NO production. Cell contact mediated effects of rMS on NO production by NR8383 cells or primary macrophages (isolated from the peritoneum of naïve Lewis rats) were tested in co-culture experiments. Therefore, rMS cells were added in increasing ratios to NR8383 cells, ranging from 1:0.02 to 1:2. Finally, effects of supernatant derived from activated NR8383 cell on rMS NO production and gene expression was explored. Results: While rMS conditioned medium was able to down regulate LPS induced NO production by macrophages in a dose dependent manner, NO production was upregulated in the co-cultures set up. Supernatant of LPS activated NR8383 induced the production of NO by rMS as well as the upregulation of iNOS gene expression, explaining the upregulation in NO production observed in the co-culture set up. Finally,rMS following incubation withsupernatant of LPS activated NR8383 supernatant upregulates molecules such as COX-2, an enzyme responsible for the production of prostaglandin E2 (PGE-2). Conclusions: rMS conditioned medium is able to down regulate the production of NO which is a hallmark of classically activated macrophages. Additionally, macrophages can prime rMS in vitro to express molecules (eg. COX-2) which are involved in PGE-2 mediated mechanisms by which stem cells can modulate the activation of macrophages . Further experiments need to be performed to confirm possible modulation of macrophage phenotype and functionality in vivo as well.
URI: http://hdl.handle.net/1942/18864
DOI: 10.2217/rme.13.op
ISSN: 1746-0751
Category: M
Type: Journal Contribution
Appears in Collections: Research publications

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