Microtubules and actin cytoskeleton of potentially pathogenic basidiomycetous yeast as targets for antifungals
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
19521073
DOI
10.1159/000224655
PII: 000224655
Knihovny.cz E-zdroje
- MeSH
- antifungální látky farmakologie MeSH
- Basidiomycota cytologie účinky léků MeSH
- bicyklické sloučeniny heterocyklické farmakologie MeSH
- cytochalasiny farmakologie MeSH
- cytokineze účinky léků MeSH
- kvasinky cytologie účinky léků MeSH
- mikrofilamenta účinky léků MeSH
- mikrotubuly účinky léků MeSH
- modulátory tubulinu farmakologie MeSH
- paclitaxel farmakologie MeSH
- spory hub účinky léků MeSH
- thiabendazol farmakologie MeSH
- thiazolidiny farmakologie MeSH
- vinblastin farmakologie MeSH
- vinkristin farmakologie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antifungální látky MeSH
- bicyklické sloučeniny heterocyklické MeSH
- cytochalasiny MeSH
- latrunculin A MeSH Prohlížeč
- modulátory tubulinu MeSH
- paclitaxel MeSH
- thiabendazol MeSH
- thiazolidiny MeSH
- vinblastin MeSH
- vinkristin MeSH
BACKGROUND: The cytoskeleton was investigated as a potential target for the inhibition of cell division in Fellomyces fuzhouensis CBS 8243 related to Cryptococcus neoformans. METHODS: Vincristine, vinblastine, paclitaxel, methyl benzimidazole-2-yl carbamate (BCM), thiabendazole, cytochalasins A, B and D and latrunculin A were added to yeast extract peptone dextrose medium containing cells, investigated by phase contrast and fluorescence microscopy, counted in a Burker chamber and absorbance was measured. RESULTS: Vincristine, vinblastine, paclitaxel, cytochalasins A, B and D transiently blocked proliferation. BCM disrupted microtubules and inhibited mitosis, but F-actin patches and cables persisted and neck-less conidia appeared without stalks. Latrunculin disrupted F-actin, cells became spherical, and stalks and necks degenerated; microtubules persisted, but mitosis, cytokinesis and conidiogenesis were blocked. The combined application of latrunculin and BCM disrupted F-actin and microtubules, and inhibited cells became spherical and did not divide. CONCLUSIONS: Microtubules and F-actin are effective targets for permanent inhibition of nuclear and cell division and conidiogenesis by BCM and latrunculin A.
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