Influence of hydroxyurea on lectin-induced early and late events in peripheral blood lymphocyte cultures
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články
PubMed
3497823
Knihovny.cz E-zdroje
- MeSH
- adenin metabolismus MeSH
- aktivace lymfocytů účinky léků MeSH
- B-lymfocyty účinky léků MeSH
- fluorescence MeSH
- hydroxymočovina farmakologie MeSH
- imunoglobuliny biosyntéza MeSH
- kultivované buňky MeSH
- lektiny farmakologie MeSH
- lidé MeSH
- lymfocyty účinky léků MeSH
- mitogeny MeSH
- thymidin metabolismus MeSH
- uridin metabolismus MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adenin MeSH
- hydroxymočovina MeSH
- imunoglobuliny MeSH
- lektiny MeSH
- mitogeny MeSH
- thymidin MeSH
- uridin MeSH
Activation events induced by lectins in human lymphocyte cultures differed not only in time kinetics of their appearance but were also in a different manner inhibited by hydroxyurea (HU). 4F2 and Tac expression, thermostable sheep erythrocyte rosette formation, cell volume distribution changes and the enhancement of the purine metabolic rate [( 3H]adenine incorporation) induced by PHA, Con A or PWM were not influenced by HU treatment, suggesting G1-phase dependency of these markers. The decrease in the mitogen-induced marker expression after 48 h of incubation with HU can be explained by the unability of activated cells to process the cell cycle, to divide and to become newly positive cells. Mitogen-induced RNA synthesis was partially, DNA synthesis, PWM-induced Ig synthesis and lectin-mediated HLA class II antigen expression were totally inhibited by HU. It holds especially for the DR antigen that its appearance in a polyclonal model of lymphocyte activation occurs in a later (postmitotic G1) phase of the cell cycle. The inhibitory effect of HU on late activation parameters could be removed after washing the cells. Mitogen-activated, HU-treated PBL cultures after removing HU continued cell cycle progression without requirement for further addition of lectin.