Hepatic stellate cells regulate hepatic progenitor cells differentiation via the TGF-β1/Jagged1 signaling axis

被引：12
作者：
Aimaiti, Yasen [1 ,2 ]
Jin, Xin [1 ]
Shao, Yue [1 ]
Wang, Wei [1 ]
Li, Dewei [1 ]
机构：
[1] Chongqing Med Univ, Dept Hepatobiliary Surg, Affiliated Hosp 1, Chongqing 400016, Peoples R China
[2] Xinjiang Med Univ, State Key Lab Pathogenesis Prevent & Treatment Hi, Urumqi, Peoples R China
来源：
JOURNAL OF CELLULAR PHYSIOLOGY | 2019年 / 234卷 / 06期
基金：
中国国家自然科学基金;
关键词：
hepatic progenitor cells; hepatic stellate cells; Jagged1; TGF-beta; 1; BILE-DUCT DEVELOPMENT; STEM-CELLS; FETAL LIVER; TRANSPLANTATION; MICE; PROLIFERATION; REGENERATION; FIBROBLASTS; EXPRESSION; HEPATOCYTES;
D O I：
10.1002/jcp.27609
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
Hepatic stellate cells (HSCs) play an important microenvironmental role in hepatic progenitor cells (HPCs) differentiation fate. To reveal the specific mechanism of HSCs induced by transforming growth factor beta 1 (TGF-beta 1) signaling in HPCs differentiation process, we used Knockin and knockdown technologies induced by lentivirus to upregulate or downregulate TGF-beta 1 level in mouse HSCs (mHSCs) (mHSCs-TGF-beta 1 or mHSCs-TGF-beta R1sih3). Primary mouse HPCs (mHPCs) were isolated and were cocultured with mHSCs-TGF-beta 1 and mHSCs-TGF-beta R1sih3 for 7 days. Differentiation of mHPCs was detected by quantitative reverse transcriptase polymerase chain reaction analysis and immunofluorence in vitro. mHPCs-E-14.5 cell lines and differently treated mHSCs were cotransplanted into mice spleens immediately after establishment of acute liver injury model for animal studies. Engraftment and differentiation of transplanted cells as well as liver function recovery were measured at the seventh day via different methods. mHSCs-TGF-beta 1 were transformed into myofibroblasts and highly expressed Jagged1, but that expression was reduced after blockage of TGF-beta 1 signaling. mHPCs highly expressed downstream markers of Jagged1/Notch signaling and cholangiocyte markers (CK19, SOX9, and Hes1) after coculture with mHSCs-TGF-beta 1 in vitro. In contrast, mature hepatocyte marker (ALB) was upregulated in mHPCs in coculture conditions with mHSCs-TGF-beta R1sih3. At the seventh day of cell transplantation assay, mHPCs-E-14.5 engrafted and differentiated into cholangiocytes after cotransplanting with TGF-beta 1-knockin mHSCs, but the cells had a tendency to differentiate into hepatocytes when transplanted with TGF-beta R1-knockdown mHSCs, which corresponded to in vitro studies. HSCs play an important role in regulating HPCs differentiation into cholangiocytes via the TGF-beta 1/Jagged1 signaling axis. However, HPCs have a tendency to differentiate into hepatocytes after blockage of TGF-beta 1 signaling in HSCs.
引用
收藏
页码：9283 / 9296
页数：14
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