Relative Contribution of PIN-Containing Secretory Vesicles and Plasma Membrane PINs to the Directed Auxin Transport: Theoretical Estimation
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články
Grantová podpora
742985
European Research Council - International
I 3630
Austrian Science Fund FWF - Austria
M 2379
Austrian Science Fund FWF - Austria
M2379-B28
Austrian Science Fund
I03630
Austrian Science Fund
PubMed
30424546
PubMed Central
PMC6274947
DOI
10.3390/ijms19113566
PII: ijms19113566
Knihovny.cz E-zdroje
- Klíčová slova
- 3D-SIM microscopy, PIN transporters, auxin, mathematical modeling, polar auxin transport, secretion,
- MeSH
- Arabidopsis metabolismus MeSH
- biologické modely * MeSH
- biologický transport MeSH
- endocytóza MeSH
- kyseliny indoloctové metabolismus MeSH
- permeabilita buněčné membrány MeSH
- proteiny huseníčku metabolismus MeSH
- sekreční vezikuly metabolismus MeSH
- zelené fluorescenční proteiny metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- kyseliny indoloctové MeSH
- proteiny huseníčku MeSH
- zelené fluorescenční proteiny MeSH
The intercellular transport of auxin is driven by PIN-formed (PIN) auxin efflux carriers. PINs are localized at the plasma membrane (PM) and on constitutively recycling endomembrane vesicles. Therefore, PINs can mediate auxin transport either by direct translocation across the PM or by pumping auxin into secretory vesicles (SVs), leading to its secretory release upon fusion with the PM. Which of these two mechanisms dominates is a matter of debate. Here, we addressed the issue with a mathematical modeling approach. We demonstrate that the efficiency of secretory transport depends on SV size, half-life of PINs on the PM, pH, exocytosis frequency and PIN density. 3D structured illumination microscopy (SIM) was used to determine PIN density on the PM. Combining this data with published values of the other parameters, we show that the transport activity of PINs in SVs would have to be at least 1000× greater than on the PM in order to produce a comparable macroscopic auxin transport. If both transport mechanisms operated simultaneously and PINs were equally active on SVs and PM, the contribution of secretion to the total auxin flux would be negligible. In conclusion, while secretory vesicle-mediated transport of auxin is an intriguing and theoretically possible model, it is unlikely to be a major mechanism of auxin transport in planta.
Institute of Science and Technology Austria Am Campus 1 3400 Klosterneuburg Austria
Mathematical Institute Faculty of Science Leiden University 2333 CA Leiden The Netherlands
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