DocumentCode :
3151407
Title :
Apop-1 Induces Caspase-Dependent Apoptosis
Author :
Sun, Xin ; Lv, Gang ; Gao, Ling ; Kong, Fanli ; Zhu, Xiaotao ; Tian, Dan ; Tong, Haibin ; Chu, Xiaodan ; Xie, Yu
Author_Institution :
Life Sci. Center, Beihua Univ. China, China
fYear :
2010
fDate :
18-20 June 2010
Firstpage :
1
Lastpage :
4
Abstract :
Apoptosis is a form of genetically programmed cell death, which plays a pivotal role in normal development and the maintenance of homeostasis of a variety of tissues including cardiovascular system. Apop-1 is a soluble protein consisting of 194 amino acids with a mitochondrial localization signal at its N-terminus. RT-PCR data revealed that Apop-1 is expressed in all the organs tested. Immunofluorescence study showed that Apop-1 protein is localized in mitochondria. Transient transfection experiment showed Apop-1 induces apoptosis of cultured VSMC, and this apoptosis is inhibited by a pan-caspase inhibitor Z-VAD. The apoptosis induced by Apop-1 may contribute to the loss of VSMC in atherosclerosis, which will influence the stability of atherosclerotic plaques.
Keywords :
blood vessels; cardiovascular system; cellular biophysics; enzymes; fluorescence; molecular biophysics; molecular configurations; Apop-1; N-terminus; RT-PCR data; amino acids; atherosclerosis; atherosclerotic plaques; biological tissues; cardiovascular system; caspase-dependent apoptosis; genetically programmed cell death; homeostasis; immunofluorescence; mitochondrial localization signal; pan-caspase inhibitor Z-VAD; protein; Amino acids; Fluorescence; Hospitals; Microscopy; Muscles; Proteins; Sliding mode control; Statistical analysis; Sun; Surgery;
fLanguage :
English
Publisher :
ieee
Conference_Titel :
Bioinformatics and Biomedical Engineering (iCBBE), 2010 4th International Conference on
Conference_Location :
Chengdu
ISSN :
2151-7614
Print_ISBN :
978-1-4244-4712-1
Electronic_ISBN :
2151-7614
Type :
conf
DOI :
10.1109/ICBBE.2010.5518003
Filename :
5518003
Link To Document :
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