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Caryologia
International Journal of Cytology, Cytosystematics and Cytogenetics
Volume 70, 2017 - Issue 2
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Articles

Programmed cell death evidence in wheat (Triticum aestivum L.) roots induced by aluminum oxide (Al2O3) nanoparticles

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Pages 112-119 | Received 07 Sep 2016, Accepted 20 Jan 2017, Published online: 14 Feb 2017

Figures & data

Table 1. The effects of Al2O3 NP (5, 25 and 50 mg ml–1) on the mitotic index, chromosome abnormalities and micronuclei in wheat roots after 96 h. The data with different letter are significantly different according to Tukey’s post-hoc HSD test for independent samples at p < 0.05. Values represent means ± SD.

Figure 1. Micronuclei and chromosomal abnormalities in Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. (a) Micronuclei in the 5 mg ml–1 (arrows) treatment; (b) C-mitosis in the 25 mg ml–1 treatment; (b) stickiness in the 25 mg ml–1 treatment; (c) monopolar metaphase in the 25 mg ml–1 treatment; (d) monopolar metaphase in the 50 mg ml–1 treatment. Scale bar = 10 μm.

Figure 1. Micronuclei and chromosomal abnormalities in Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. (a) Micronuclei in the 5 mg ml–1 (arrows) treatment; (b) C-mitosis in the 25 mg ml–1 treatment; (b) stickiness in the 25 mg ml–1 treatment; (c) monopolar metaphase in the 25 mg ml–1 treatment; (d) monopolar metaphase in the 50 mg ml–1 treatment. Scale bar = 10 μm.

Figure 2. Immunostaining of microtubule structures in control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. (a) Control; (b) 5 mg ml–1; (c) 25 mg ml–1; (d) 50 mg ml–1. Arrows show microtubule disruption. Scale bar = 50 μm.

Figure 2. Immunostaining of microtubule structures in control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. (a) Control; (b) 5 mg ml–1; (c) 25 mg ml–1; (d) 50 mg ml–1. Arrows show microtubule disruption. Scale bar = 50 μm.

Figure 3. Loss of plasma membrane integrity in control and Al NP-treated wheat roots after 96 h. All data are significantly different from the control at the p < 0.05 level.

Figure 3. Loss of plasma membrane integrity in control and Al NP-treated wheat roots after 96 h. All data are significantly different from the control at the p < 0.05 level.

Figure 4. Control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat root cells stained with DAPI. (a) Spherical nucleus in control. (b–d) Nucleus degenerations (arrow) in (b) the 5 mg ml–1 treatment; (c) the 25 mg ml–1 treatment; and (d) the 50 mg ml–1 treatment. Scale bar = 10 μm.

Figure 4. Control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat root cells stained with DAPI. (a) Spherical nucleus in control. (b–d) Nucleus degenerations (arrow) in (b) the 5 mg ml–1 treatment; (c) the 25 mg ml–1 treatment; and (d) the 50 mg ml–1 treatment. Scale bar = 10 μm.

Figure 5. TUNEL staining of control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. a. Control (no reaction), b. 5 mg ml–1 c. 25 mg ml–1 d. 50 mg ml–1. Arrows show TUNEL positive nuclei. Scale bar = 50 μm.

Figure 5. TUNEL staining of control and Al2O3 NP (5, 25 and 50 mg ml–1) treated wheat roots after 96 h. a. Control (no reaction), b. 5 mg ml–1 c. 25 mg ml–1 d. 50 mg ml–1. Arrows show TUNEL positive nuclei. Scale bar = 50 μm.

Figure 6. The % fold increase of caspase-3, -8 and -9 activities in control and Al NP-treated wheat roots after 96 h.

Figure 6. The % fold increase of caspase-3, -8 and -9 activities in control and Al NP-treated wheat roots after 96 h.

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