Apical-root apoplastic acidification affects cell-wall extensibility in wheat under salinity stress

Plant salt tolerance is closely associated with a high rate of root growth. Although root growth is governed by cell-wall and apoplastic pH, the relationship between these factors in the root elongation zone under salinity stress remains unclear. Here, we assess apoplastic pH, pH- and expansin-dependent cell-wall extensibility, and expansin expression in the root elongation zone of salt-sensitive (Yongliang-15) and -tolerant (JS-7) cultivars under salinity stress. A six-day 80 mM NaCl treatment significantly reduced apical-root apoplastic pH, from 6.2 to 5.3, in both cultivars. Using a pH-dependent cell-wall extensibility experiment, we found that, under 0 mM NaCl treatment, the optimal pH for cell-wall loosening was 6.0 in the salinity-tolerant cultivar and 4.6 in the salinity-sensitive cultivar. Under 80 mM treatment, a pH of 5.0 mitigated the cell-wall stiffness caused by salinity stress in the salinity-tolerant cultivar, but promoted cell-wall stiffening in the salinity-sensitive cultivar. These changes in pH-dependent cell-wall extensibility are consistent with differences in the root growth of two cultivars under salinity stress. Exogenous expansin application, and expansin expression experiments, we found that salinity stress altered expansin expression, differentially affecting cell-wall extensibility under pH 5.0 and 6.0. TaEXPA7 and TaEXPA8 induced cell-wall loosening at pH 5.0, whereas TaEXPA5 induced cell-wall loosening at pH 6.0. These results elucidate the relationship between expansin and cell-wall extensibility in the root elongation zone, with important implications for enhancing plant growth under salinity stress.

Effects of lead toxicity on growth and cell wall extensibility in rice seedlings

The effect of lead (Pb) on growth and mechanical properties of cell wall was investigated in rice seedlings. Caryopses of rice were germinated and grown in various concentrations of lead nitrate for 5 days at 250C in the dark. Growth of rice seedlings was suppressed by Pb ions; significant suppression was caused by low concentration of Pb as 1 μM. Growth suppression was prominent in roots, but not clear in shoot organs, such as coleoptiles or first leaves, suggesting that roots are the primary target of Pb toxicity. The analysis of the cell wall extensibility of rice roots grown in Pb solution indicated that the cell wall extensibility was greatly decreased with increased concentration of Pb ions. These results suggest that Pb may influence the synthesis of cell wall polysaccharides, thereby decreasing the cell wall extensibility, resulting in growth suppression in rice roots.

In vitro cell wall extensibility controls age-related changes in the growth rate of etiolated Arabidopsis hypocotyls

Plant cell growth is controlled by cell wall extensibility, which is currently estimated indirectly by various microtensile and nano/microindentation techniques. Their outputs differ in the accuracy of growth rate and in vivo extensibility prediction. Using the creep method we critically tested several metrics (creep rate, creep rate × stress–1, in vitro cell wall extensibility (ϕ) and in vitro cell wall yield threshold (y)) for their ability to predict growth rates of etiolated Arabidopsis thaliana (L. Heynh.) hypocotyls. We developed novel approaches for ϕ and y determination and statistical analysis based on creep measurements under single loads coupled with wall stress calculation. The best indicator of growth rate was ϕ because the 3-fold developmental decrease in the growth rate of 4- vs 3-day-old hypocotyls was accompanied by a 3-fold decrease in ϕ determined at pH 5. Although the acid-induced expansin-mediated creep of cell walls resulted exclusively from increasing ϕ values, the decrease in ϕ between 3- and 4-day-old hypocotyls was not mediated by a decrease in expansin abundance. We give practical recommendations on the most efficient use of creep rate, creep rate × stress–1, ϕ and y in different experimental situations and provide scripts for their automated calculations and statistical comparisons.

Simple method to estimate cell wall extensibility coefficient by using only two cardinal numbers

In this short communication we consider the extensibility properties of the cell wall. This is accomplished by a heuristically motivated equation for the expanding volume of the cell. The experimentally determined characteristic time t0 and temperature T0 are the only numbers required for evaluating the effective yielding coefficient Ф(t, T) in the respective time and temperature domains.