Evidence map›Paper›PMID 29170436›Full record

ArticleScientific reports2017

Fate tracing of hepatocytes in mouse liver.

Xiaowen Gu, Danyi Huang, Lei Ci, Jiahao Shi, Mengjie Zhang, Hua Yang, Zhugang Wang, Zhejin Sheng, Ruilin Sun, Jian Fei

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Single Cell Analysis Reveals the Presence of Novel Intermediate Cells in Both Mice and Patients With Severe MASLD.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Vitamin A: too good to be bad?Frontiers in pharmacology · 2023
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Xiaowen GuSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Danyi HuangSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Lei CiSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Jiahao ShiSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Mengjie ZhangSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Hua YangSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Zhugang WangShanghai Engineering Research Center for Model Organisms, SRCMO/SMOC, Shanghai, 201203, China.
Zhejin ShengSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China.
Ruilin SunShanghai Engineering Research Center for Model Organisms, SRCMO/SMOC, Shanghai, 201203, China.
Jian FeiSchool of Life Science and Techonology, Tongji University, Shanghai, 200092, China. jfei@tongji.edu.cn.ORCID 0000-0001-7755-0818
Tongji University · CNShanghai Model Organisms (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocytes perform most of the functions of the liver and are considered terminally differentiated cells. Recently, it has been suggested that hepatocytes might have the potential to transdifferentiate or dedifferentiate under physiological or pathological conditions in vivo. Epithelial-mesenchymal transition of hepatocytes in liver fibrosis has also been proposed. However, these findings have not been fully confirmed. In this study, hepatocytes were genetically labelled for cell fate tracing using lacZ via the tamoxifen-induced CreERT/loxP system. After induction with tamoxifen, alb + cells were permanently marked by lacZ expression, and all progeny lacZ + cells were derived from a single source with no interference. We did not observe transdifferentiation or dedifferentiation of hepatocytes into cholangiocytes or hepatic progenitor cells under conditions of liver homeostasis or following a 2/3 partial hepatectomy. Meanwhile, lacZ/OPN-positive cells were observed in livers of 3,5-diethoxycarbonyl-1,4-dihydrocollidine-fed mice, and lacZ/alpha-smooth muscle actin-positive cells were detected in carbon tetrachloride-induced chronic liver injury models. These results suggested that some existing differentiated alb + cells might have the potential of transdifferentiation/dedifferentiation or epithelial-to-mesenchymal transition in vivo in some liver injury models, but the proportion of these alb + cells in liver was very low, and their significance and actual function during the pathological process remains to be elucidated.

Indexed as

AnimalsCarbon TetrachlorideCell DifferentiationEpithelial-Mesenchymal TransitionHepatic Stellate CellsHepatocytesLiverLiver CirrhosisLiver RegenerationMaleMiceMice, Inbred C57BLTamoxifenCarbon TetrachlorideTamoxifen

Identifiers

PMID29170436
PMCPMC5701080
OpenAlexW2770309577

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.