IntroductionCadmium (Cd) has become one of the most harmful and widespread pollutants in water and soils caused by industrial emissions, the application of Cd-containing phosphate fertilizers, and municipal waste disposal [1]. It can easily be absorbed and accumulated in plant roots, and roots are the first organ in which plants contact this element in Cd-polluted soil [2]. The toxicity of Cd is associated with inhibitory interactions between numerous physiological and metabolic processes, such as interference in mitosis [3][4], toxicity to nucleoli structure [5][6][7], and influence on the organization of microtubular cytoskeleton and tubulin assembly/disassembly processes [7]. To prevent an excess of heavy metals in the metabolically active cytoplasm and organelles, the defence mechanisms come into operation, allowing for detoxification of harmful metal levels at the cellular level, including Cd exclusion, binding, and precipitation in the Pol.
AbstractThe toxic effects of Cd on microtubule (MT) organization in root tip cells of S. matsudana were investigated in the present study using tubulin immunolabeling and fluorescence microscopy. Cell damage and expression level of the SmTUA1 gene in the root tips were also examined by means of propidium iodide (PI) staining and quantitative real-time PCR (qRT-PCR) technology. The MT arrays were very sensitive to Cd. At interphase, under 50 μmol/L Cd treatment for 48 h, some cortical MTs were discontinuous, inducing numbers of differently sized fragments. With increased Cd concentrations and duration of treatment, peripheral MTs appeared to be broken gradually, and the degree of disorder was enhanced. Spindle fibers even formed condensed MT at 10 µmol/L Cd for 48 h. During anaphase/telophase, there was a small part of MT absent, MT fibers were stuck to each other (even forming lumps) and could not form phragmoplast at 50 µmol/L Cd for 48 h. The cell damage of S. matsudana root tips increased with enhanced Cd concentrations and prolonged treatment time. Expression level of SmTUA1 analyzed by qRT-PCR further validated the results by indirect immunofluorescence staining. The data obtained here will be very useful to understand the mechanisms of Cd-induced cell toxicity.