[Transmembrane transport of K+ and Cl- during pollen grain activation in vivo and in vitro].

We studied the possibility of K+ and Cl- efflux from tobacco pollen grains during their activation in vitro or on the stigma of a pistil. For this purpose the X-ray microanalysis and spectrofluorometry were applied. We found that the relative content of potassium and chlorine in the microvolume of pollen grain decreases during its hydration and activation on stigma. Efflux of these ions was found both in vivo and in vitro. In model in vitro experiments anion channel inhibitor NPPB ((5-nitro-2-(3-phenylpropylamino) benzoic acid) in the concentration that was blocking pollen germination, reduced Cl- efflux; potassium channel inhibitor (tetraethylammonium chloride) partially reduced K+ efflux and lowered the percent of activated cells. Another blocker of potassium channels Ba2+ caused severe decrease in cell volume and blocked the activation. In general, the obtained data demonstrates that the initiation of pollen germination both in vivo and in vitro involves the activation of K+ and Cl- release. An important role in these processes is played by NPPB-, TEA- and Ba(2+)-sensitive plasmalemma ion channels.

[Antioxidant properties of the pollen exine polymer matrix].

The antioxidant properties of exine polymer matrix which forms the outer layer of pollen grain wall were studied. The main component of this matrix is sporopollenin - a unique biopolymer resistant to mechanical and chemical damage. The samples of isolated exine, purified from soluble compounds, were studied with EPR using stable nitroxyl radical TEMPO and DMPO spin trap. At the same time, we analyzed changes in fluorescence of DCFH which detected ROS in the solution. It has been established that exine effectively reduces TEMPO radical and eliminates hydroxyl radical. Also, the fluorometric analysis demonstrated that the exine eliminated H2O2, and this ability significantly decreased after treatment of exine with feruloyl esterase or mild alkaline hydrolysis (1M NaOH), i.e. after hydrolysis of hydroxycinnamic acid esters. After harsh hydrolysis (4M NaOH, 170 degrees C) of ethers bonds a large amount of hydroxycinnamic acids has been released, and exines have lost their antioxidant capacity almost completely. The obtained results point to the ability of extracellular polymer matrix of the exine to eliminate free radicals and H2O2 during crucial periods of male gametophyte development. The participation of ferulic acid and, possibly, of other hydroxycinnamic acids of sporopollenin in these processes has been demonstrated.

[Another discussion of membrane voltage alterations in growing pollen tube].

Here we give a critical analysis of the opinion of Andreev (2011) on membrane potential distribution along the pollen tube plasmalemma. He assumes that a lateral gradient of dipole potential exists, but suggests a lateral gradient of transmembrane potential impossible. We demonstrate by concrete examples that the argumentation of the initiator of discussion is based on inaccurate citation of our experimental data (Breygina et al., 2009) and incomplete analysis of previously published articles. Speaking about transmembrane potential, he doesn't consider numerous facts demonstrating the uneven distribution of transmembrane ion fluxes and ion-transport proteins in the pollen tube plasmalemma, as well as data obtained by modeling of transmembrane potential distribution in objects of different shape. In addition, the assumption on the uneven distribution of dipole potential doesn't have an experimental basis neither in studies of the pollen tube, nor in the practice of using fluorescent voltage-sensitive dyes DiBAC4(3) and Di-4-ANEPPS. We are expecting the author to obtain experimental data in support of his position.

[Effects of anion channel blockers NPPB and DIDS on tobacco pollen tube growth and its mitochondria state].

Influence of anion channel blockers NPPB and DIDS on pollen tube growth and its mitochondria functioning was studied by means of fluorescence microscopy and flow cytometry. NPPB (40 microM) blocked pollen tube growth completely, but did not change its diameter. DIDS (20-80 microM) caused pollen tube swelling and bursting, suggesting that DIDS-sensitive channels take part in the regulation of pollen tube osmotic balance. The osmotic effect of low DIDS concentration (20 (Mkappa)M) was not accompanied by changes in the tube growth rate. The mapping of membrane potential on the pollen tube plasmalemma using Di-4-ANEPPS revealed the involvement of NPPB-sensitive but not DIDS-sensitive anion channels in the maintenance of the longitudinal membrane potential gradient along the tube surface. The study of isolated pollen mitochondria showed that DIDS increased their capacity to take up potential-dependent dye DiOC5(3), i. e. caused hyperpolarization of mitochondrial membranes. At the same time DIDS influenced on intramitochondrial ROS content and excretion of ROS from mitochondria. Thus, NPPB and DIDS differently influenced on transmembrane potential distribution along pollen tube plasmalemma, on its osmotic balance, and on mitochondria functioning. This set of data suggests that pollen tube growth is dependent on activity of anion channels that differ in localization and functions.

[Membrane potential changes during pollen germination and tube growth].

We applied quantitative fluorescent microscopy to study membrane potential alterations during pollen germination and in growing pollen tube. Two voltage-sensitive dyes were applied: DiBAC4(3) was used to detect average membrane potential values in pollen grains and isolated protoplasts; Di-4-ANEPPS gave an option of membrane potential mapping on pollen protoplast and pollen tube surfaces. We have found out that tobacco pollen grain activation is accompanied by hyperpolarization of the vegetative cell plasma membrane by about 8 mV. Lily pollen protoplasts were significantly hyperpolarized (-108 mV) with respect to the pollen grains (-23 mV) from which they were isolated. We found polar distribution of the membrane potential along the protoplast surface, and longitudinal potential gradient along the pollen tube. In the presence of plasma membrane H(+)-ATPase inhibitor, sodium orthovanadate (1 mM) or its activator fusicoccin (1 microM), the longitudinal voltage gradient altered but did not disappear. Anion channel blocker, NPPB (40 microM), fully discarded the gradient in pollen tubes. Obtained results give evidence of the plasma membrane hyperpolarization during pollen germination and uneven potential distribution on pollen grain and tube surfaces. Inhibitory analysis showed involvement of the plasma membrane H(+)-ATPase and anion channels in membrane potential regulation.