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A key role of boron in plants is to cross-link the cell wall pectic polysaccharide rhamnogalacturonan-II (RG-II) through borate diester linkages. Phenylboronic acid (PBA) can form the same reversible ester bonds but cannot cross-link two molecules, so can be used as an antagonist to study the function of boron. This study aimed to evaluate the effect of PBA on apple (Malus domestica) pollen tube growth and the underlying regulatory mechanism. We observed that PBA caused an inhibition of pollen germination, tube growth and led to pollen tube morphological abnormalities. Fluorescent labeling, coupled with a scanning ion-selective electrode technique, revealed that PBA induced an increase in extracellular Ca2+ influx, thereby elevating the cytosolic Ca2+ concentration [Ca2+]c and disrupting the [Ca2+]c gradient, which is critical for pollen tube growth. Moreover the organization of actin filaments was severely perturbed by the PBA treatment. Immunolocalization studies and fluorescent labeling, together with Fourier-transform infrared analysis (FTIR) suggested that PBA caused an increase in the abundance of callose, de-esterified pectins and arabinogalactan proteins (AGPs) at the tip. However, it had no effect on the deposition of the wall polymers cellulose. These effects are similar to those of boron deficiency in roots and other organs, indicating that PBA can induce boron deficiency symptoms. The results provide new insights into the roles of boron in pollen tube development, which likely include regulating [Ca2+]c and the formation of the actin cytoskeleton, in addition to the synthesis and assembly of cell wall components.

Aluminum (Al) is an important element in soil constitution. Previous studies have shown that high concentration of Al affects the normal growth of crops, resulting in crop yield reduction and inferior quality. Nevertheless, Al has also been referred to as a beneficial element, especially when used at low concentrations, but the cytological mechanism is not clear. Influences of low concentration AlCl3 on the pollen tube growth of apple (Malus domestica) and its possible cytological mechanism were investigated in this study. The results showed that 20 μM AlCl3 promoted pollen germination and tube elongation; 20 μM AlCl3 enhanced Ca2+ influx but did not affect [Ca2+]c of the pollen tube tip; and 20 μM AlCl3 decreased acid pectins in pollen tubes but increased esterified pectins and arabinan pectins in pollen tubes. According to the information provided in this research, 20 μM AlCl3 stimulated growth of pollen tubes by enhancing Ca2+ influx and changing cell wall components. [ABSTRACT FROM AUTHOR]

Abstract: Heterotrimeric G proteins are involved in a variety of cellular responses, but relatively little is known about their function and biochemistry in plant pollen. In this paper, we establish the presence of a G protein associated with the plasma membranes of Pinus bungeana pollen tube. A 40kDa polypeptide is detected and immunolocalized predominantly in pollen tube plasma membranes by polyclonal antisera directed against conserved peptides of mammalian Gα-subunit during pollen tube development. Cholera and pertussis toxins exhibited biphasic actions on tube growth, that is to say, inhibited pollen tube growth and result in rupture of tubes at concentrations less than 400ngmL−1, whereas stimulated pollen tube growth at concentration over 500ngmL−1. Fourier transform-infrared (FT-IR) spectra showed that the two toxins at concentrations of 400ngmL−1 resulted in enhanced synthesis of phenolics and reduced synthesis of cellulose, hemicellulose, and xylan of pollen tube wall, which may account for incidental rupture of pollen tubes at the concentration. These results suggest that the two toxins possibly affect pollen tube growth via downstream pertussis or cholera toxin-sensitive functional proteins, which regulate tube wall biosynthesis than at the Gα-subunit in P. bungeana tube growth. [Copyright &y& Elsevier]

• Al inhibits pollen germination and tube growth. • Al toxicity affects pollen tube apex calcium influx and [Ca2+]c gradient. • Al toxicity alters actin filament orientation. • Al toxicity affects pollen tube wall components. Aluminum (Al) is known the most abundant metal in the Earth's crust which is a major problem limiting crop production and yield throughout the world. Al could inhibit pollen tube elongation, however the mechanism is largely unknown. The aim of this study was to investigate the influence of Al toxicity on Malus domestica pollen tube growth and possible cytological mechanism. The results showed that Al inhibited pollen germination and tube growth in a concentration dependent manner. An non-invasive ion-selective electrode technique together with fluorescent labeling indicated that Al toxicity decreased pollen tube apex calcium influx and disrupted [Ca2+]c gradient. Al toxicity also altered actin filament orientation. Results from immuno-localization and fluorescence labeling indicated that Al toxicity affected the accumulation and distribution of callose, acid pectins, esterified pectins and arabinogalactan proteins in pollen tubes, which were supported by Fourier-transform infrared analysis. In a word, Al induced a series of the cellular toxic changes concerning calcium influx, [Ca2+]c gradient, actin and cell wall components. Based on the information provided in this article, it is concluded that Al toxicity inhibits apical growth of pollen tubes by changing calcium influx and [Ca2+]c and cell wall components. [ABSTRACT FROM AUTHOR]

Abstract: The Rac/Rop small GTPases are central regulators of important cellular processes in plants. But their roles in pollen and pollen tube development in plants are still not well understood, especially in gymnosperms. In the present paper, a 23-kDa polypeptide was detected in pollen tube plasma membrane and cytosolic fractions in Picea willsonii pollen tubes using the antisera against the NtRac1 protein and Arabidopsis Rops. The Rac1 protein appears to be associated with the plasma membrane based on detergent experiments. Subcellular localization using indirect immunofluorescence and confocal microscopy showed that the detected Rac1 is concentrated in the cortical region of the tube apex, especially in the growing fast tubes, and that little is present in arrested tubes. Interestingly, a Rac/Rop protein was observed in the tube nucleus and sperm cells of P. willsonii pollen tubes, and almost little exist while these cells inside pollen grains. These results suggest that Rac/Rop GTPases are involved in the signaling mechanism that controls pollen tube growth and might point to a potential function in signaling to the migration of the tube nucleus and sperm cells in pollen tubes in P. willsonii. [Copyright &y& Elsevier]