中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Genetic tracing of hepatocytes in liver homeostasis, injury, and regeneration

文献类型:期刊论文

作者Wang, Yue1,2; Huang, XiuZhen1,2; He, Lingjuan1,2; Pu, Wenjuan1,2; Li, Yan1,2; Liu, Qiaozhen1,2; Li, Yi1,2; Zhang, Libo1,2; Yu, Wei1,2; Zhao, Huan1,2
刊名JOURNAL OF BIOLOGICAL CHEMISTRY
出版日期2017
卷号292期号:21页码:8594-8604
ISSN号0021-9258
关键词PI3K Peptide Therapy Gastric cancers Mouse model
DOI10.1074/jbc.M117.782029
文献子类Article
英文摘要The liver possesses a remarkable capacity to regenerate after damage. There is a heated debate on the origin of new hepatocytes after injuries in adult liver. Hepatic stem/progenitor cells have been proposed to produce functional hepatocytes after injury. Recent studies have argued against this model and suggested that pre-existing hepatocytes, rather than stem cells, contribute new hepatocytes. This hepatocyte-to-hepatocyte model is mainly based on labeling of hepatocytes with Cre-recombinase delivered by the adeno-associated virus. However, the impact of virus infection on cell fate determination, consistency of infection efficiency, and duration of Cre-virus in hepatocytes remain confounding factors that interfere with the data interpretation. Here, we generated a new genetic tool Alb-DreER to label almost all hepatocytes (>99.5%) and track their contribution to different cell lineages in the liver. By pulse-and-chase strategy, we found that pre-existing hepatocytes labeled by Alb-DreER contribute to almost all hepatocytes during normal homeostasis and after liver injury. Virtually all hepatocytes in the injured liver are descendants of pre-existing hepatocytes through self-expansion. We concluded that stem cell differentiation is unlikely to be responsible for the generation of a substantial number of new hepatocytes in adult liver. Our study also provides a new mouse tool for more precise in vivo genetic study of hepatocytes in the field.
学科主题Biochemistry & Molecular Biology
WOS关键词PROGENITOR CELLS ; MOUSE-LIVER ; PERIPORTAL HEPATOCYTES ; MATURE HEPATOCYTES ; STEM-CELLS ; RISE ; DIFFERENTIATION ; CHOLANGIOCYTES ; CONTRIBUTES ; RATHER
语种英语
出版者AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
WOS记录号WOS:000402153900008
版本出版稿
源URL[http://202.127.25.144/handle/331004/976]  
专题中国科学院上海生命科学研究院营养科学研究所
作者单位1.Univ Chinese Acad Sci, CAS Ctr Excellence Mol Cell Sci, Shanghai Inst Biochem & Cell Biol, State Key Lab Cell Biol,Chinese Acad Sci, Shanghai 200031, Peoples R China;
2.Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Biol Sci, Key Lab Nutr & Metab,Inst Nutr Sci, Shanghai 200031, Peoples R China;
3.Tongji Univ, Sch Med, Shanghai Peoples Hosp 10, Dept Gastroenterol, 301 Yanchang Rd, Shanghai 200072, Peoples R China;
4.Jinan Univ, Inst Aging & Regenerat Med, Minist Educ, Key Lab Regenerat Med, Guangzhou 510632, Guangdong, Peoples R China;
5.ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China,
推荐引用方式
GB/T 7714
Wang, Yue,Huang, XiuZhen,He, Lingjuan,et al. Genetic tracing of hepatocytes in liver homeostasis, injury, and regeneration[J]. JOURNAL OF BIOLOGICAL CHEMISTRY,2017,292(21):8594-8604.
APA Wang, Yue.,Huang, XiuZhen.,He, Lingjuan.,Pu, Wenjuan.,Li, Yan.,...&,.(2017).Genetic tracing of hepatocytes in liver homeostasis, injury, and regeneration.JOURNAL OF BIOLOGICAL CHEMISTRY,292(21),8594-8604.
MLA Wang, Yue,et al."Genetic tracing of hepatocytes in liver homeostasis, injury, and regeneration".JOURNAL OF BIOLOGICAL CHEMISTRY 292.21(2017):8594-8604.

入库方式: OAI收割

来源:上海营养与健康研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。