scholarly journals Diatom motility and nuclear alterations are affected by sediment elutriates of agricultural streams

2020 ◽  
Vol 205 ◽  
pp. 111322
Author(s):  
M.M. Nicolosi Gelis ◽  
M.A. Mujica ◽  
A. Pecile ◽  
J. Donadelli ◽  
M. Simonetti ◽  
...  
Author(s):  
Sara Sandström ◽  
Martyn N. Futter ◽  
David W. O'Connell ◽  
Emma E. Lannergård ◽  
Jelena Rakovic ◽  
...  

2021 ◽  
Vol 286 ◽  
pp. 112193
Author(s):  
Joachim Audet ◽  
Trine Mariane Olsen ◽  
Thomas Elsborg ◽  
Annette Baattrup-Pedersen ◽  
Tenna Riis
Keyword(s):  

Author(s):  
Jennifer L. Tank ◽  
Shannon L. Speir ◽  
Lienne R. Sethna ◽  
Todd V. Royer
Keyword(s):  

2015 ◽  
Vol 290 (34) ◽  
pp. 20841-20855 ◽  
Author(s):  
Mercè Garcia-Belinchón ◽  
María Sánchez-Osuna ◽  
Laura Martínez-Escardó ◽  
Carla Granados-Colomina ◽  
Sònia Pascual-Guiral ◽  
...  

Apoptosis is triggered by the activation of caspases and characterized by chromatin condensation and nuclear fragmentation (type II nuclear morphology). Necrosis is depicted by a gain in cell volume (oncosis), swelling of organelles, plasma membrane leakage, and subsequent loss of intracellular contents. Although considered as different cell death entities, there is an overlap between apoptosis and necrosis. In this sense, mounting evidence suggests that both processes can be morphological expressions of a common biochemical network known as “apoptosis-necrosis continuum.” To gain insight into the events driving the apoptosis-necrosis continuum, apoptotically proficient cells were screened facing several apoptotic inducers for the absence of type II apoptotic nuclear morphologies. Chelerythrine was selected for further studies based on its cytotoxicity and the lack of apoptotic nuclear alterations. Chelerythrine triggered an early plasma membrane leakage without condensed chromatin aggregates. Ultrastructural analysis revealed that chelerythrine-mediated cytotoxicity was compatible with a necrotic-like type of cell death. Biochemically, chelerythrine induced the activation of caspases. Moreover, the inhibition of caspases prevented chelerythrine-triggered necrotic-like cell death. Compared with staurosporine, chelerythrine induced stronger caspase activation detectable at earlier times. After using a battery of chemicals, we found that high concentrations of thiolic antioxidants fully prevented chelerythrine-driven caspase activation and necrotic-like cell death. Lower amounts of thiolic antioxidants partially prevented chelerythrine-mediated cytotoxicity and allowed cells to display type II apoptotic nuclear morphology correlating with a delay in caspase-3 activation. Altogether, these data support that an early and pronounced activation of caspases can drive cells to undergo a form of necrotic-like regulated cell death.


Hydrobiologia ◽  
1989 ◽  
Vol 174 (2) ◽  
pp. 89-97 ◽  
Author(s):  
M. D. Munn ◽  
L. L. Osborne ◽  
M. J. Wiley

2018 ◽  
Vol 2018 ◽  
pp. 1-11 ◽  
Author(s):  
Javier Morán-Martínez ◽  
Roberto Beltrán del Río-Parra ◽  
Nadia Denys Betancourt-Martínez ◽  
Rubén García-Garza ◽  
Joel Jiménez-Villarreal ◽  
...  

For the EPD, different voltages and different times were used. Male rats were used in four groups (n=3) with different treatments. The blood sample was obtained for genotoxic analysis and liver and kidney organs were removed for histopathological analysis. The amount of NPs TiO2 deposited on the samples of the arches increases gradually in the times of 15 and 30 s. At all voltages, however, at 45, 60, 75, and 90 s, there is an increase up to 25 V. Cell viability in lymphocytes treated with TiO2 NPs did not cause genotoxicity. In the histopathological findings of hepatic and renal tissue, nuclear alterations and necrosis were observed. The objective of the study was to improve the physical and biocompatibility characteristics of the NiTi arches for which the EPD is used. The technique for the deposition of TiO2 NPs was used, where this technique could be used as an economical and versatile way to perform homogeneous depositions even on surfaces with the complexity of the NiTi alloy. As for genotoxicity and cytotoxicity, we continue to have controversial results.


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