<p>(A) Morphological alterations in cerebral cortical neurons treated with different concentrations of Cd (0, 5, 10 and 20 µM) for 24 h. Cell morphology was assessed using a LEICA inverted phase-contrast microscope (400×) equipped with Quick Imaging system. All experiments were performed in duplicate. (B) Cell viability of cerebral cortical neurons, treated with 0–25 µM Cd for 12 and 24 h, was evaluated by MTT assay. Results are presented as mean ± SD (n = 6). *Statistical significance between control and Cd treatment (2.5, 5, 10, 20 and 25 µM); *<i>P</i><0.05, **<i>P</i><0.01 compared to respective control, using Student’s t-test. (C) Cd induced apoptotic morphological changes in cerebral cortical neurons. Cerebral cortical neurons were in...
Background: Cladribine (2-CdA) can cross the blood–brain barrier, resulting in inhibition of DNA syn...
<p>A shows immunocytochemical analysis of apoptosis (TUNEL staining) in cortical neuronal cultures i...
<p>DAPI staining of primary cortical neurons was carried out at 24 hours after OGD. Typical apoptoti...
<p>(A) Morphological alterations in cerebral cortical neurons treated with/without Cd (10 µM) in the...
<p>(A and B) Cd increased cleavage of caspase-9, caspase-3 and PARP. Cells were exposed to 0–20 µM C...
<p>(A and B) PC12 cells were treated with 0–20 µM Cd for 24 h, or with 0, 10 and 20 µM Cd for 0–24 h...
<p>Indicated cells were pretreated with/without BAPTA/AM at indicated concentrations for 30 min, and...
<p>Cortical neurons were treated with U18666A. <b>A</b>) Filipin staining and differential interfere...
<p>Cells were pretreated with BAPTA-AM (10 µM) for 30 min, followed by treatment with Cd for another...
<p>(<b>A</b>) Representative micrographs of neurons treated or not with 20 µM of glutamate and 10 µM...
<p>Cortical neurons were pre-treated with Roscovitine or CR8 (CDK1 inhibitors) or vehicle and then e...
Cadmium (Cd) is an extremely toxic metal, capable of severely damaging several organs, including the...
<p>Cells were exposed to CdCl<sub>2</sub> (5 and 10 μM) for 24 h in the absence or presence of NAC (...
<p>(<i>A</i>) Left: Confocal images of TUNEL-stained cells in the neocortex of control and cDKO mice...
<p>Microglia, astrocytes and neurons (4x10<sup>5</sup>/well in 12-well plates) were cultivated under...
Background: Cladribine (2-CdA) can cross the blood–brain barrier, resulting in inhibition of DNA syn...
<p>A shows immunocytochemical analysis of apoptosis (TUNEL staining) in cortical neuronal cultures i...
<p>DAPI staining of primary cortical neurons was carried out at 24 hours after OGD. Typical apoptoti...
<p>(A) Morphological alterations in cerebral cortical neurons treated with/without Cd (10 µM) in the...
<p>(A and B) Cd increased cleavage of caspase-9, caspase-3 and PARP. Cells were exposed to 0–20 µM C...
<p>(A and B) PC12 cells were treated with 0–20 µM Cd for 24 h, or with 0, 10 and 20 µM Cd for 0–24 h...
<p>Indicated cells were pretreated with/without BAPTA/AM at indicated concentrations for 30 min, and...
<p>Cortical neurons were treated with U18666A. <b>A</b>) Filipin staining and differential interfere...
<p>Cells were pretreated with BAPTA-AM (10 µM) for 30 min, followed by treatment with Cd for another...
<p>(<b>A</b>) Representative micrographs of neurons treated or not with 20 µM of glutamate and 10 µM...
<p>Cortical neurons were pre-treated with Roscovitine or CR8 (CDK1 inhibitors) or vehicle and then e...
Cadmium (Cd) is an extremely toxic metal, capable of severely damaging several organs, including the...
<p>Cells were exposed to CdCl<sub>2</sub> (5 and 10 μM) for 24 h in the absence or presence of NAC (...
<p>(<i>A</i>) Left: Confocal images of TUNEL-stained cells in the neocortex of control and cDKO mice...
<p>Microglia, astrocytes and neurons (4x10<sup>5</sup>/well in 12-well plates) were cultivated under...
Background: Cladribine (2-CdA) can cross the blood–brain barrier, resulting in inhibition of DNA syn...
<p>A shows immunocytochemical analysis of apoptosis (TUNEL staining) in cortical neuronal cultures i...
<p>DAPI staining of primary cortical neurons was carried out at 24 hours after OGD. Typical apoptoti...