Vital Staining- Chemistry and its Application in Dentistry

2021 ◽  
pp. 53-61
Author(s):  
K. Nitya ◽  
Vikram S. Amberkar ◽  
V. Keerthi Narayan ◽  
R. Ramya ◽  
S. Sneha ◽  
...  
Keyword(s):  
2000 ◽  
Vol 279 (3) ◽  
pp. H939-H945 ◽  
Author(s):  
Shareef Mustapha ◽  
Alla Kirshner ◽  
Danielle De Moissac ◽  
Lorrie A. Kirshenbaum

Nuclear factor-κB (NF-κB) is a ubiquitously expressed cellular factor regulated by the cytoplasmic factor inhibitor protein κBα (IκBα). Activation of NF-κB by cytokines, including tumor necrosis factor-α (TNF-α), requires the phosphorylation and degradation of IκBα. An anti-apoptotic role for NF-κB has recently been suggested. In the present study, we ascertained whether death-promoting signals and apoptosis mediated by TNF-α are suppressed by NF-κB in postnatal ventricular myocytes. Stimulation of myocytes with TNF-α resulted in a 12.1-fold increase ( P < 0.01) in NF-κB-dependent gene transcription and DNA binding compared with controls. This was accompanied by a corresponding increase in the NF-κB target protein A20 as determined by Western blot analysis. Vital staining revealed that TNF-α was not cytotoxic to myocytes and did not provoke apoptosis. Adenovirus-mediated delivery of a nonphosphorylatable form of IκBα to inactivate NF-κB prevented TNF-α-stimulated NF-κB-dependent gene transcription and nuclear NF-κB DNA binding. Importantly, myocytes stimulated with TNF-α and defective for NF-κB activation resulted in a 2.2-fold increase ( P < 0.001) in apoptosis. To our knowledge, the data provide the first indication that a functional NF-κB signaling pathway is crucial for suppressing death-promoting signals mediated by TNF-α in ventricular myocytes.


2007 ◽  
Vol 25 (4) ◽  
pp. 426-427
Author(s):  
D Rawat ◽  
MR Capoor ◽  
A Hasan ◽  
D Nair ◽  
M Deb ◽  
...  
Keyword(s):  

Biomolecules ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 866
Author(s):  
Luong Huu Dang ◽  
Yuan Tseng ◽  
How Tseng ◽  
Shih-Han Hung

In this study, we developed a new procedure for the rapid partial decellularization of the harvested trachea. Partial decellularization was performed using a combination of detergent and sonication to completely remove the epithelial layers outside of the cartilage ring. The post-decellularized tracheal segments were assessed with vital staining, which showed that the core cartilage cells remarkably remained intact while the cells outside of the cartilage were no longer viable. The ability of the decellularized tracheal segments to evade immune rejection was evaluated through heterotopic implantation of the segments into the chest muscle of rabbits without any immunosuppressive therapy, which demonstrated no evidence of severe rejection or tissue necrosis under H&E staining, as well as the mechanical stability under stress-pressure testing. Finally, orthotopic transplantation of partially decellularized trachea with no immunosuppression treatment resulted in 2 months of survival in two rabbits and one long-term survival (2 years) in one rabbit. Through evaluations of posttransplantation histology and endoscopy, we confirmed that our partial decellularization method could be a potential method of producing low-immunogenic cartilage scaffolds with viable, functional core cartilage cells that can achieve long-term survival after in vivo transplantation.


PROTOPLASMA ◽  
1961 ◽  
Vol 53 (1) ◽  
pp. 57-75 ◽  
Author(s):  
J. Zurzycki ◽  
W. Starzecki
Keyword(s):  

1972 ◽  
Vol 13 (2) ◽  
pp. 156 ◽  
Author(s):  
David M. Dressel ◽  
Donald R. Heinle ◽  
Marlene C. Grote
Keyword(s):  

1968 ◽  
Vol 10 ◽  
pp. 119b-120
Author(s):  
Kennosuke TAKEZAKO ◽  
Hitoshi ICHIKI ◽  
Yoshiaki OKUMA ◽  
Tetsuya SHIRAO ◽  
Akira SAKAMOTO ◽  
...  

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