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A local application of mesenchymal stem cells and cyclosporine A attenuates immune response by a switch in macrophage phenotype

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F17%3A00454064" target="_blank" >RIV/68378041:_____/17:00454064 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/17:10320407

  • Result on the web

    <a href="http://dx.doi.org/10.1002/term.2044" target="_blank" >http://dx.doi.org/10.1002/term.2044</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/term.2044" target="_blank" >10.1002/term.2044</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A local application of mesenchymal stem cells and cyclosporine A attenuates immune response by a switch in macrophage phenotype

  • Original language description

    The immunosuppressive effects of systemically administered mesenchymal stem cells (MSCs) and immunosuppressive drugs have been well documented. We analysed the mechanisms underlying the therapeutic effect of MSCs applied locally in combination with non-specific immunosuppression in a mouse model of allogeneic skin transplantation. The MSC-seeded and cyclosporine A (CsA)-loaded nanofibre scaffolds were applied topically to skin allografts in a mouse model and the local immune response was assessed and characterized. MSCs migrated from the scaffold into the side of injury and were detected in the graft region and draining lymph nodes (DLNs). The numbers of graft-infiltrating macrophages and the production of nitric oxide (NO) were significantly decreased in recipients treated with MSCs and CsA, and this reduction correlated with impaired production of IFN. in the graft and DLNs. In contrast, the proportion of alternatively activated macrophages (F4/80(+)CD206(+) cells) and the production of IL-10 by intragraft macrophages were significantly upregulated. The ability of MSCs to alter the phenotype of macrophages from the M1 type into an M2 population was confirmed in a co-culture system in vitro. We suggest that the topical application of MSCs in combination with CsA induces a switch in macrophages to a population with an alternatively activated 'healing' phenotype and producing elevated levels of IL-10. These alterations in macrophage phenotype and function could represent one of the mechanisms of immunosuppressive action of MSCs applied in combination with CsA.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10601 - Cell biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2017

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Tissue Engineering and Regenerative Medicine

  • ISSN

    1932-6254

  • e-ISSN

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    10

  • Pages from-to

    1456-1465

  • UT code for WoS article

    000402987500013

  • EID of the result in the Scopus database

    2-s2.0-84933574461