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The Immune Phenotype of ThreeDrosophilaLeukemia Models
B. Arefin, M. Kunc, R. Krautz, U. Theopold,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2011
Freely Accessible Science Journals
od 2011-06-01 do 2020
PubMed Central
od 2011
Europe PubMed Central
od 2011
Open Access Digital Library
od 2011-01-01
Open Access Digital Library
od 2011-01-01
Oxford Journals Open Access Collection
od 2011-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2011
PubMed
28476910
DOI
10.1534/g3.117.039487
Knihovny.cz E-zdroje
- MeSH
- Drosophila MeSH
- fenotyp * MeSH
- hemocyty imunologie MeSH
- kachexie * genetika imunologie MeSH
- larva genetika imunologie MeSH
- leukemie * genetika imunologie MeSH
- modely nemocí na zvířatech MeSH
- přirozená imunita * MeSH
- proteiny Drosophily genetika imunologie MeSH
- protoonkogenní proteiny p21(ras) genetika imunologie MeSH
- zvířata MeSH
- Check Tag
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
Many leukemia patients suffer from dysregulation of their immune system, making them more susceptible to infections and leading to general weakening (cachexia). Both adaptive and innate immunity are affected. The fruit flyDrosophila melanogasterhas an innate immune system, including cells of the myeloid lineage (hemocytes). To studyDrosophilaimmunity and physiology during leukemia, we established three models by driving expression of a dominant-active version of the Ras oncogene (RasV12) alone or combined with knockdowns of tumor suppressors inDrosophilahemocytes. Our results show that phagocytosis, hemocyte migration to wound sites, wound sealing, and survival upon bacterial infection of leukemic lines are similar to wild type. We find that in all leukemic models the two major immune pathways (Toll and Imd) are dysregulated. Toll-dependent signaling is activated to comparable extents as after wounding wild-type larvae, leading to a proinflammatory status. In contrast, Imd signaling is suppressed. Finally, we notice that adult tissue formation is blocked and degradation of cell masses during metamorphosis of leukemic lines, which is akin to the state of cancer-dependent cachexia. To further analyze the immune competence of leukemic lines, we used a natural infection model that involves insect-pathogenic nematodes. We identified two leukemic lines that were sensitive to nematode infections. Further characterization demonstrates that despite the absence of behavioral abnormalities at the larval stage, leukemic larvae show reduced locomotion in the presence of nematodes. Taken together, this work establishes newDrosophilamodels to study the physiological, immunological, and behavioral consequences of various forms of leukemia.
Citace poskytuje Crossref.org
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