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Description
  • V této studii jsme analyzovali aktivační děje způsobené dimery FcepsilonRI, vyvolané vazbou mAb anti-FcepsilonRI proti krysím bazofilním leukemickým buňkám. Zjistili jsme, že na rozdíl od silně agregovaných FcepsiloRI dimery receptoru (1) indukovaly slabší spojení FcepsilonRI s membránami odolnými vůči detergentům, (2) zpomalovaly fosforylaci tyrozinu a membránovou mobilizaci řady signalizačních molekul, (3) vyvolávaly pomalejší, ale soustavnější zvyšování koncentrace volného cytoplasmatického vápníku, (4) vyvolávaly degranulaci, která nebyla při vyšších koncentracích křížově vázané mAb potlačována a (5) nebyly schopny produkovat shluky FcepsilonRI, kinázy Syk a adaptoru Grb2 v osmiofilních membránách, jak bylo zjištěno elektronovou mikroskopií využívající imunitní reakce se zlatem na membránových vrstvách. Přes výrazné rozdíly v topografii dimerů a multimerů FcepsilonRI byly biochemické rozdíly méně výrazné. Z kombinovaných dat vyplývá, že žírné buňky aktivované FcepsilonRI přenáše... (cs)
  • In this study, we analyzed the activation events induced by FcepsilonRI dimers, elicited by binding of anti-FcepsilonRI mAb to rat basophilic leukemia cells. We found that, in contrast to extensively aggregated FcepsilonRI, receptor dimers (1) induced a less extensive association of FcepsilonRI with detergent-resistant membranes, (2) delayed the tyrosine phosphorylation and membrane recruitment of several signaling molecules, (3) triggered a slower but more sustained increase in concentration of free cytoplasmic calcium, (4) induced degranulation which was not inhibited at higher concentrations of the cross-linking mAb, and (5) failed to produce clusters of FcepsilonRI, Syk kinase and Grb2 adapter in osmiophilic membranes, as detected by immunogold electron microscopy on membrane sheets. Despite striking differences in the topography of FcepsilonRI dimers and multimers, biochemical differences were less pronounced. The combined data suggest that FcepsilonRI-activated mast cells prop...
  • In this study, we analyzed the activation events induced by FcepsilonRI dimers, elicited by binding of anti-FcepsilonRI mAb to rat basophilic leukemia cells. We found that, in contrast to extensively aggregated FcepsilonRI, receptor dimers (1) induced a less extensive association of FcepsilonRI with detergent-resistant membranes, (2) delayed the tyrosine phosphorylation and membrane recruitment of several signaling molecules, (3) triggered a slower but more sustained increase in concentration of free cytoplasmic calcium, (4) induced degranulation which was not inhibited at higher concentrations of the cross-linking mAb, and (5) failed to produce clusters of FcepsilonRI, Syk kinase and Grb2 adapter in osmiophilic membranes, as detected by immunogold electron microscopy on membrane sheets. Despite striking differences in the topography of FcepsilonRI dimers and multimers, biochemical differences were less pronounced. The combined data suggest that FcepsilonRI-activated mast cells prop... (en)
Title
  • Signaling assemblies formed in mast cells activated via Fce receptor I dimers
  • Signalizační soustavy tvořené v žírných buňkách aktivovaných dimery Fce receptoru I (cs)
  • Signaling assemblies formed in mast cells activated via Fce receptor I dimers (en)
skos:prefLabel
  • Signaling assemblies formed in mast cells activated via Fce receptor I dimers
  • Signalizační soustavy tvořené v žírných buňkách aktivovaných dimery Fce receptoru I (cs)
  • Signaling assemblies formed in mast cells activated via Fce receptor I dimers (en)
skos:notation
  • RIV/68378050:_____/04:00109000!RIV/2005/AV0/A23005/N
http://linked.open.../vavai/riv/strany
  • 2209;2219
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • P(GA204/00/0204), P(GA204/03/0594), P(GA301/03/0596), P(GA310/00/0205), P(IAA5052005), P(IAA5052310), P(IAA7052006), P(LN00A026), Z(AV0Z5052915)
http://linked.open...iv/cisloPeriodika
  • 8
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
http://linked.open.../riv/druhVysledku
http://linked.open...iv/duvernostUdaju
http://linked.open...titaPredkladatele
http://linked.open...dnocenehoVysledku
  • 586166
http://linked.open...ai/riv/idVysledku
  • RIV/68378050:_____/04:00109000
http://linked.open...riv/jazykVysledku
http://linked.open.../riv/klicovaSlova
  • mast cell; protein kinase; IgE receptor (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • DE - Spolková republika Německo
http://linked.open...ontrolniKodProRIV
  • [2FE24CF4B331]
http://linked.open...i/riv/nazevZdroje
  • European Journal of Immunology
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...vavai/riv/projekt
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 34
http://linked.open...iv/tvurceVysledku
  • Štokrová, Jitka
  • Dráber, Petr
  • Dráberová, Lubica
  • Hálová, Ivana
  • Korb, Jan
  • Lebduška, Pavel
  • Tolar, Pavel
  • Tolarová, Helena
http://linked.open...n/vavai/riv/zamer
issn
  • 0014-2980
number of pages
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