Oscillatory chloride efflux at the pollen tube apex has a role in growth and cell volume regulation and is targeted by inositol 3,4,5,6-tetrakisphosphate
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
12215517
Knihovny.cz E-zdroje
- MeSH
- buněčné dělení účinky léků MeSH
- chloridové kanály metabolismus MeSH
- chloridy metabolismus MeSH
- inositolfosfáty farmakologie MeSH
- kyselina 4,4'-diisothiokyanostilben-2,2'-disulfonová farmakologie MeSH
- kyselina niflumová farmakologie MeSH
- lilie cytologie účinky léků růst a vývoj MeSH
- nitrobenzoany farmakologie MeSH
- pyl účinky léků růst a vývoj metabolismus MeSH
- tabák cytologie účinky léků růst a vývoj MeSH
- velikost buňky účinky léků MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 5-nitro-2-(3-phenylpropylamino)benzoic acid MeSH Prohlížeč
- chloridové kanály MeSH
- chloridy MeSH
- inositol-1,3,4,5-tetrakisphosphate MeSH Prohlížeč
- inositol-1,3,4,5,6-pentakisphosphate MeSH Prohlížeč
- inositol-3,4,5,6-tetrakisphosphate MeSH Prohlížeč
- inositolfosfáty MeSH
- kyselina 4,4'-diisothiokyanostilben-2,2'-disulfonová MeSH
- kyselina niflumová MeSH
- nitrobenzoany MeSH
Oscillatory growth of pollen tubes has been correlated with oscillatory influxes of the cations Ca(2+), H(+), and K(+). Using an ion-specific vibrating probe, a new circuit was identified that involves oscillatory efflux of the anion Cl(-) at the apex and steady influx along the tube starting at 12 microm distal to the tip. This spatial coupling of influx and efflux sites predicts that a vectorial flux of Cl(-) ion traverses the apical region. The Cl(-) channel blockers 4,4'-diisothiocyanatostilbene-2,2'-disulfonic acid (DIDS) and 5-nitro-2-(3-phenylpropylamino)benzoic acid completely inhibited tobacco pollen tube growth at 80 and 20 microM, respectively. Cl(-) channel blockers also induced increases in apical cell volume. The apical 50 micro m of untreated pollen tubes had a mean cell volume of 3905 +/- 75 microm(3). DIDS at 80 microM caused a rapid and lethal cell volume increase to 6206 +/- 171 microm(3), which is at the point of cell bursting at the apex. DIDS was further demonstrated to disrupt Cl(-) efflux from the apex, indicating that Cl(-) flux correlates with pollen tube growth and cell volume status. The signal encoded by inositol 3,4,5,6-tetrakisphosphate [Ins(3,4,5,6)P(4)] antagonized pollen tube growth, induced cell volume increases, and disrupted Cl(-) efflux. Ins(3,4,5,6)P(4) decreased the mean growth rate by 85%, increased the cell volume to 5997 +/- 148 microm(3), and disrupted normal Cl(-) efflux oscillations. These effects were specific for Ins(3,4,5,6)P(4) and were not mimicked by either Ins(1,3,4,5)P(4) or Ins(1,3,4,5,6)P(5). Growth correlation analysis demonstrated that cycles of Cl(-) efflux were coupled to and temporally in phase with cycles of growth. A role for Cl(-) flux in the dynamic cellular events during growth is assessed. Differential interference contrast microscopy and kymographic analysis of individual growth cycles revealed that vesicles can advance transiently to within 2 to 4 microm of the apex during the phase of maximally increasing Cl(-) efflux, which temporally overlaps the phase of cell elongation during the growth cycle. In summary, these investigations indicate that Cl(-) ion dynamics are an important component in the network of events that regulate pollen tube homeostasis and growth.
State and spectral properties of chloride oscillations in pollen