Role of Cytoskeleton Proteins in the Morphological Changes During Apoptotic Cell Death of Cerebellar Granule Neurons

2010 ◽  
Vol 36 (1) ◽  
pp. 93-102 ◽  
Author(s):  
Alette Ortega ◽  
Julio Morán
2004 ◽  
Vol 29 (1) ◽  
pp. 227-238 ◽  
Author(s):  
A. Franco-Cea ◽  
A. Valencia ◽  
S. Sánchez-Armass ◽  
G. Domínguez ◽  
J. Morán

2009 ◽  
Vol 87 (1) ◽  
pp. 190-199 ◽  
Author(s):  
Yutaka Ikeno ◽  
So-hyun Cheon ◽  
Naoko Konno ◽  
Ayako Nakamura ◽  
Katsuhiko Kitamoto ◽  
...  

2000 ◽  
Vol 288 (3) ◽  
pp. 167-170 ◽  
Author(s):  
Makoto Ohgoh ◽  
Kazuto Yamazaki ◽  
Hiroo Ogura ◽  
Yukio Nishizawa ◽  
Isao Tanaka

2019 ◽  
Vol 25 (05) ◽  
pp. 1263-1272 ◽  
Author(s):  
Shanmugapriya ◽  
Soundararajan Vijayarathna ◽  
Sreenivasan Sasidharan

AbstractSeveral microscopy methods have been developed to assess the morphological changes in cells in the investigations of the mode of cell death in response to a stimulus. Our recent finding on the treatment of the IC50 concentration (26.67 μg/mL) of Polyalthia longifolia leaf extract indicated the induction of apoptotic cell death via the regulation of miRNA in HeLa cells. Hence, the current study was conducted to validate the function of these downregulated microRNAs in P. longifolia-treated HeLa cells using microscopic approaches. These include scanning electron microscope (SEM), transmission electron microscope (TEM), and acridine orange/propidium iodide (AO/PI)-based fluorescent microscopy techniques by observing the morphological alterations to cells after transfection with mimic miRNA. Interestingly, the morphological changes observed in this study demonstrated the apoptotic hallmarks, for instance, cell blebbing, cell shrinkage, cytoplasmic and nuclear condensation, vacuolization, cytoplasmic extrusion, and the formation of apoptotic bodies, which proved the role of dysregulated miRNAs in apoptotic HeLa cell death after treatment with the P. longifolia leaf extract. Conclusively, the current study proved the crucial role of downregulated miR-484 and miR-221-5p in the induction of apoptotic cell death in P. longifolia-treated HeLa cells using three approaches—SEM, TEM, and AO/PI-based fluorescent microscope.


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