ACTIVATION AND REGULATION OF RESERVE LIVER PROGENITOR CELLS

被引:2
作者
Best, D. Hunter [1 ,2 ]
Coleman, William B. [3 ]
机构
[1] Univ Utah, Sch Med, Dept Pathol, Salt Lake City, UT 84112 USA
[2] ARUP Labs Inc, Div Genet, Salt Lake City, UT USA
[3] Univ N Carolina, Sch Med, Dept Pathol & Lab Med, Curriculum Toxicol,Program Translat Med,UNC Lineb, Chapel Hill, NC USA
来源
VITAMINS AND HORMONES: STEM CELL REGULATORS | 2011年 / 87卷
关键词
NECROSIS-FACTOR-ALPHA; GROWTH-FACTOR-ALPHA; RATS FED N-2-FLUORENYLACETAMIDE; PROTEIN-TYROSINE-PHOSPHATASE; MESSENGER-RNA EXPRESSION; OVAL CELLS; CYCLE PROGRESSION; STEM-CELLS; IN-VIVO; CARBON-TETRACHLORIDE;
D O I
10.1016/B978-0-12-386015-6.00026-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The mammalian liver possesses an extraordinary capacity for regeneration of tissue mass and cell numbers following loss of hepatocytes due to partial tissue loss (surgical resection) or hepatotoxic injury (necrosis). Restoration of liver mass can be obtained through the outgrowth and expansion of a number of different cell types depending upon the nature and extent of injury and/or tissue deficit. In an otherwise healthy liver, the replacement of hepatocytes (and tissue mass) is achieved through the proliferation of differentiated, normally quiescent hepatocytes contained in the residual (viable) tissue. However, in certain forms of liver injury, the capacity of differentiated hepatocytes to proliferate in response to liver tissue deficit is significantly impaired. When this occurs, reserve stem-like progenitor cells are activated to proliferate and replace lost hepatocytes. In this review, we will discuss the currently available information regarding the activation and outgrowth of each of these liver progenitor cell populations. (C) 2011 Elsevier Inc.
引用
收藏
页码:93 / 109
页数:17
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