Actin stabilization induces apoptosis in cultured porcine epithelial cell rests of Malassez
Autor: | Takashi Muramatsu, F. Kobayashi, Masataka Suehara, Natsuko Aida, Ryo Sako, T. Ushikubo, Masahiro Furusawa |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Cell Survival Periodontal Ligament Swine Phalloidin Apoptosis Biology 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Depsipeptides Fluorescence microscope Animals Viability assay Tooth Root Fragmentation (cell biology) General Dentistry Cells Cultured Actin Alexa Fluor Epithelial Cells 030206 dentistry Epithelial cell rests of Malassez Actins Cell biology 030104 developmental biology chemistry |
Zdroj: | International Endodontic Journal. 49:663-669 |
ISSN: | 0143-2885 |
DOI: | 10.1111/iej.12494 |
Popis: | Aim To test whether actin stabilization by jasplakinolide induces inhibition of cell viability and apoptosis in epithelial cell rests of Malassez (ERM). Methodology ERM derived from porcine were spread in a 96-well dish (5 × 104/well) using Dulbecco's modified Eagle's medium. The actin-specific stabilization reagent, jasplakinolide, was incorporated into the culture medium and incubated for 24 h. To evaluate cell viability, the WST-1 assay was carried out and absorption (450 nm) was measured. To detect apoptotic cells, monoclonal antibody to single-strand DNA (ssDNA) was used and absorption (405 nm) was measured. Actin stabilization and apoptosis induced by jasplakinolide were morphologically investigated by staining with Alexa Fluor 568 phalloidin and observed under a fluorescent microscope. As a negative control, DMSO was used instead of jasplakinolide. Differences between the jasplakinolide-treated group and the control group were analysed statistically using the Student's t-test. Results Cell viability decreased in a concentration-dependent manner, and cell viability in the jasplakinolide-treated ERM was lower than that in nontreated ERM (n = 16, P |
Databáze: | OpenAIRE |
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