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TcpC induces apoptosis of human vascular endothelial cells and its mechanisms / 浙江大学学报·医学版
Article de Zh | WPRIM | ID: wpr-252600
Bibliothèque responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the effects of TcpC on human umbilical vascular endothelial cells (HUVECs) and its mechanisms.</p><p><b>METHODS</b>HUVECs were co-cultured with TcpC secreting wild-type E. coli strain CFT073 (TcpC(wt)) or tcpc gene-deleted CFT073 mutant strain (TcpC(mut)) in transwell system,respectively. Apoptosis of HUVECs was analyzed by Annexin-V/PI double staining. Mitochondrial membrane depolarization was detected by JC-1 staining. Expression of apoptosis-related proteins in HUVECs was determined by Western blot.</p><p><b>RESULTS</b>HUVECs showed morphological changes after co-cultured with TcpC(wt) for 24 h: the cells became detached and cell debris increased,and cell number was also decreased when compared to HUVECs co-cultured with TcpC(mut). The apoptosis of HUVEC cells co-cultured with TcpC(wt) for 24 h significantly increased,compared to that of control group and TcpC(mut) group (60.1% 9.7% compared with 9.0% 1.3% and 16.9% 0.4%,respectively, P<0.05); meanwhile the mitochondrial depolarization of HUVECs co-cultured with TcpC(wt) was significantly increased,compared to that in control and TcpC(mut) groups (64.5% 0.9% compared with 14.5% 2.1% and 15.6% 3.3%, respectively,P<0.05). Cleavage of PARP and inhibition of Mcl-1 and XIAP expression were seen in HUVECs co-cultured with TcpC(wt),but not in groups of control and TcpC(mut).</p><p><b>CONCLUSION</b>TcpC secreted from CFT073 can induce apoptosis of HUVECs through mitochondrial pathway, in which PARP is cleaved and Mcl-1 and XIAP expressions are inhibited.</p>
Sujet(s)
Texte intégral: 1 Indice: WPRIM Sujet Principal: Anatomopathologie / Pharmacologie / Cellules cultivées / Poly(ADP-ribose) polymerases / Apoptose / Protéines Escherichia coli / Facteurs de virulence / Escherichia coli / Protéine inhibitrice de l&apos;apoptose liée au chromosome X / Potentiel de membrane mitochondriale Limites du sujet: Humans langue: Zh Texte intégral: Journal of Zhejiang University. Medical sciences Année: 2013 Type: Article
Texte intégral: 1 Indice: WPRIM Sujet Principal: Anatomopathologie / Pharmacologie / Cellules cultivées / Poly(ADP-ribose) polymerases / Apoptose / Protéines Escherichia coli / Facteurs de virulence / Escherichia coli / Protéine inhibitrice de l&apos;apoptose liée au chromosome X / Potentiel de membrane mitochondriale Limites du sujet: Humans langue: Zh Texte intégral: Journal of Zhejiang University. Medical sciences Année: 2013 Type: Article