"The Good, the Bad, and the Ugly" - About Diverse Phenotypes of Hepatic Stellate Cells in the Liver

被引:4
作者
Bogomolova, Alexandra [1 ,2 ]
Balakrishnan, Asha [1 ]
Ott, Michael [1 ,4 ]
Sharma, Amar Deep [1 ,3 ]
机构
[1] Hannover Med Sch, Dept Gastroenterol Hepatol Infect Dis & Endocrinol, Hannover, Germany
[2] Hannover Med Sch, REBIRTH Res Ctr Translat Regenerat Med, Res Grp RNA Therapeut & Liver Regenerat, Hannover, Germany
[3] Med Hsch Hannover Gastroenterol Hepatol & Endocrin, Carl Neuberg Str 1, D-39625 Hannover, Germany
[4] Hannover Med Sch, Dept Gastroenterol Hepatol Infect Dis & Endocrinol, Carl Neuberg Str 1, D-30625 Hannover, Germany
来源
CELLULAR AND MOLECULAR GASTROENTEROLOGY AND HEPATOLOGY | 2024年 / 17卷 / 04期
关键词
ANTIGEN-PRESENTING CELLS; HEPATOCELLULAR-CARCINOMA; TARGETED DELIVERY; GENE-THERAPY; MESENCHYMAL TRANSITION; FIBROSIS; CANCER; MYOFIBROBLASTS; HEPATOCYTES; INCREASES;
D O I
10.1016/j.jcmgh.2024.01.002
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Hepatic stellate cells (HSCs) and their activated derivatives, often referred to as myofibroblasts (MFs), play a key role in progression of chronic liver injuries leading to fibrosis, cirrhosis, and hepatocellular carcinoma. Until recently, MFs were considered a homogenous cell type majorly due to lack of techniques that allow complex molecular studies at a single -cell resolution. Recent technical advancements in genetic lineage-tracing models as well as the exponential growth of studies with single -cell transcriptome and proteome analyses have uncovered hidden heterogeneities among the HSC and MF populations in healthy states as well as chronic liver injuries at the various stages of tissue deformation. The identification of different phenotypes along the HSC/MF axis, which either maintain essential liver functions ("good" HSCs), emerge during fibrosis ("bad" HSCs), or even promote hepatocellular carcinoma ("ugly" HSCs), may lay the foundation for targeting a particular MF phenotype as potential treatment for chronic liver injuries.
引用
收藏
页码:607 / 622
页数:16
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