Chronological protein synthesis in regenerating rat liver

被引:6
|
作者
He, Jinjun [1 ]
Hao, Shuai [1 ]
Zhang, Hao [1 ]
Guo, Fuzheng [1 ]
Huang, Lingyun [1 ]
Xiao, Xueyuan [1 ]
He, Dacheng [1 ]
机构
[1] Beijing Normal Univ, Minist Educ, Key Lab Cell Proliferat & Regulat Biol, Univ Confederated Inst Prote, Beijing 100875, Peoples R China
关键词
Dynamic proteomics; Liver regeneration; Protein synthesis velocity; Pulse labeling; PARTIAL-HEPATECTOMY; GENE-EXPRESSION; PROTEOMIC ANALYSIS; BETA-CATENIN; VITAMIN-D; C-FOS; ACTIVATION; TURNOVER; PHOSPHORYLATION; PROLIFERATION;
D O I
10.1002/elps.201500019
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liver regeneration has been studied for decades; however, its regulation remains unclear. In this study, we report a dynamic tracing of protein synthesis in rat regenerating liver with a new proteomic technique, S-35 in vivo labeling analysis for dynamic proteomics (SiLAD). Conventional proteomic techniques typically measure protein alteration in accumulated amounts. The SiLAD technique specifically detects protein synthesis velocity instead of accumulated amounts of protein through S-35 pulse labeling of newly synthesized proteins, providing a direct way for analyzing protein synthesis variations. Consequently, protein synthesis within short as 30 min was visualized and protein regulations in the first 8 h of regenerating liver were dynamically traced. Further, the 3.5-5 h post partial hepatectomy (PHx) was shown to be an important regulatory turning point by acute regulation of many proteins in the initiation of liver regeneration.
引用
收藏
页码:1622 / 1632
页数:11
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