Nitric oxide and cytokine production by glial cells exposed in vitro to neuropathogenic schistosome Trichobilharzia regenti
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F16%3A10329226" target="_blank" >RIV/00216208:11310/16:10329226 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1186/s13071-016-1869-7" target="_blank" >http://dx.doi.org/10.1186/s13071-016-1869-7</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1186/s13071-016-1869-7" target="_blank" >10.1186/s13071-016-1869-7</a>
Alternative languages
Result language
angličtina
Original language name
Nitric oxide and cytokine production by glial cells exposed in vitro to neuropathogenic schistosome Trichobilharzia regenti
Original language description
This study was focused on astrocytes and microglia as these are immunocompetent cells of the nervous tissue and their activation was recently observed in Trichobilharzia regenti-infected mice. Results: Primary astrocytes and microglia were exposed to several stimulants of T. regenti origin. Living schistosomulum-like stages caused increased secretion of IL-6 in astrocyte cultures, but no changes in nitric oxide (NO) production were noticed. Nevertheless, elevated parasite mortality was observed in these cultures. Soluble fraction of the homogenate from schistosomulum-like stages stimulated NO production by both astrocytes and microglia, and IL-6 and TNF-alpha secretion in astrocyte cultures. Similarly, recombinant cathepsins B1.1 and B2 triggered IL-6 and TNF-alpha release in astrocyte and microglia cultures, and NO production in astrocyte cultures. Stimulants had no effect on production of anti-inflammatory cytokines IL-10 or TGF-beta 1. Conclusions: Both astrocytes and microglia are capable of production of NO and proinflammatory cytokines IL-6 and TNF-a following in vitro exposure to various stimulants of T. regenti origin. Astrocytes might be involved in triggering the tissue inflammation in the early phase of T. regenti infection and are proposed to participate in destruction of migrating schistosomula. However, NO is not the major factor responsible for parasite damage. Both astrocytes and microglia can be responsible for the nervous tissue pathology and maintaining the ongoing inflammation since they are a source of NO and proinflammatory cytokines which are released after exposure to parasite antigens.
Czech name
—
Czech description
—
Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
EC - Immunology
OECD FORD branch
—
Result continuities
Project
<a href="/en/project/GA13-29577S" target="_blank" >GA13-29577S: The neurotropic schistosome Trichobilharzia regenti in vertebrates: immune response, pathology and diagnostic markers</a><br>
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2016
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Parasites and Vectors
ISSN
1756-3305
e-ISSN
—
Volume of the periodical
9
Issue of the periodical within the volume
NOV 14 2016
Country of publishing house
GB - UNITED KINGDOM
Number of pages
10
Pages from-to
—
UT code for WoS article
000388145600003
EID of the result in the Scopus database
2-s2.0-84994777619