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Effects of Newcastle disease virus on the mitochondria of human gastric carcinoma BGC-823 cells / 中华实验和临床病毒学杂志
Article de Zh | WPRIM | ID: wpr-254105
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To explore changes in structure and function of the mitochondria of human gastric carcinoma BGC-823 cells after Newcastle disease virus (NDV) infection.</p><p><b>METHODS</b>Electron microscopy was applied to observe the structure of mitochondria; Rhodamine 123 staining was used to determine the mitochondrial membrane potential; the activity of Na(+)-K(+)-ATPase and Ca(2+)-ATPase were also determined and the release of cytochrome C was detected by Western blotting.</p><p><b>RESULTS</b>The structure of mitochondria in the tumor cells infected with NDV changed distinctly. In the infected group the activity of mitochondrial Na(+)-K(+)-ATPase and Ca(2+)-ATPase significantly declined (P < 0.01), and compared with control cells, mitochondrial trans-membrane potential was decreased. NDV infection induced the decrease of cytochrome C levels.</p><p><b>CONCLUSION</b>The effects of NDV infection on the structure and functions of mitochondria of human gastric carcinoma BGC-823 cells might play a role in the oncolysis of NDV.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Physiologie / Tumeurs de l&apos;estomac / Virologie / Virus de la maladie de Newcastle / Carcinomes / Sodium-Potassium-Exchanging ATPase / Lignée cellulaire tumorale / Cytochromes c / Potentiel de membrane mitochondriale / Métabolisme Limites du sujet: Animals / Humans langue: Zh Texte intégral: Chinese Journal of Experimental and Clinical Virology Année: 2008 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Physiologie / Tumeurs de l&apos;estomac / Virologie / Virus de la maladie de Newcastle / Carcinomes / Sodium-Potassium-Exchanging ATPase / Lignée cellulaire tumorale / Cytochromes c / Potentiel de membrane mitochondriale / Métabolisme Limites du sujet: Animals / Humans langue: Zh Texte intégral: Chinese Journal of Experimental and Clinical Virology Année: 2008 Type: Article