Ergosterol elicits oxidative burst in tobacco cells via phospholipase A2 and protein kinase C signal pathway
Jazyk angličtina Země Francie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
15191747
DOI
10.1016/j.plaphy.2004.04.003
PII: S0981-9428(04)00060-9
Knihovny.cz E-zdroje
- MeSH
- bílkoviny řas farmakologie MeSH
- časové faktory MeSH
- ergosterol farmakologie MeSH
- estreny farmakologie MeSH
- fosfolipasy A antagonisté a inhibitory metabolismus MeSH
- fosfolipasy A2 MeSH
- fosfolipasy typu C antagonisté a inhibitory MeSH
- fungální proteiny MeSH
- inhibitory enzymů farmakologie MeSH
- isochinoliny farmakologie MeSH
- kultivované buňky MeSH
- neomycin farmakologie MeSH
- oxidační stres * MeSH
- proteinkinasa C metabolismus MeSH
- pyrrolidinony farmakologie MeSH
- signální transdukce MeSH
- sulfonamidy * MeSH
- tabák účinky léků metabolismus MeSH
- viabilita buněk MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 1-(6-((3-methoxyestra-1,3,5(10)-trien-17-yl)amino)hexyl)-1H-pyrrole-2,5-dione MeSH Prohlížeč
- bílkoviny řas MeSH
- cryptogein protein, Phytophthora cryptogea MeSH Prohlížeč
- ergosterol MeSH
- estreny MeSH
- fosfolipasy A MeSH
- fosfolipasy A2 MeSH
- fosfolipasy typu C MeSH
- fungální proteiny MeSH
- inhibitory enzymů MeSH
- isochinoliny MeSH
- N-(2-(4-bromocinnamylamino)ethyl)-5-isoquinolinesulfonamide MeSH Prohlížeč
- neomycin MeSH
- proteinkinasa C MeSH
- pyrrolidinony MeSH
- sulfonamidy * MeSH
Ergosterol, a typical fungal sterol, induced in tobacco (Nicotiana tabacum L. cv. Xanthi) suspension cells the synthesis of reactive oxygen species and alkalization of the external medium that are dependent on the mobilization of calcium from internal stores. We used specific inhibitors to elucidate the signal pathway triggered by ergosterol compared with cryptogein, a proteinaceous elicitor of Phytophthora cryptogea. Herbimycin A and genistein, inhibitors of tyrosine protein kinases, had no effect on the oxidative burst and pH changes induced by both elicitors. Similarly, H-89, an inhibitor of protein kinase A, had no effect on the induction of these defense reactions. However, the response to both elicitors was completely blocked by NPC-15437, a specific inhibitor of animal protein kinase C (PKC). The responses induced by cryptogein but not those induced by ergosterol were inhibited by U73122 and neomycin, inhibitors of phospholipase C (PLC). On the other hand, the activity of phospholipase A2 (PLA2) measured using a fluorogenic substrate was stimulated by ergosterol and not by cholesterol and cryptogein. A specific inhibitor of PLA2, arachidonic acid trifluoromethyl ketone (AACOCF3), inhibited the pathway stimulated by ergosterol but not that induced by cryptogein. These results suggest that the cryptogein-induced signal pathway leading to the oxidative burst and DeltapH changes includes PLC and PKC, whereas this response induced by ergosterol includes PLA2 and PKC.
Citace poskytuje Crossref.org
Ergosterol treatment leads to the expression of a specific set of defence-related genes in tobacco
Nonspecific elicitation of defense reaction in suspension tobacco cells by elicitors from Armillaria