Evidence map›Paper›PMID 28330992›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2017

Localized hepatic lobular regeneration by central-vein-associated lineage-restricted progenitors.

Jonathan M Tsai, Pang Wei Koh, Ania Stefanska, Liujing Xing, Graham G Walmsley, Nicolas Poux, Irving L Weissman, Yuval Rinkevich

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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

8 authors at 2 institutions in 2 countries.

Jonathan M TsaiInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305.
Pang Wei KohDepartment of Genetics, Stanford University School of Medicine, Stanford, CA 94305.
Ania StefanskaComprehensive Pneumology Center, Institute of Lung Biology and Disease, Helmholtz Zentrum München, 81377 Munich, Germany.
Liujing XingInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305.
Graham G WalmsleyInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305.ORCID 0000-0002-9706-8356
Nicolas PouxInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305.
Irving L WeissmanInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305; irv@stanford.edu yuval.rinkevich@helmholtz-muenchen.de.
Yuval RinkevichComprehensive Pneumology Center, Institute of Lung Biology and Disease, Helmholtz Zentrum München, 81377 Munich, Germany; irv@stanford.edu yuval.rinkevich@helmholtz-muenchen.de.
Stanford University · USHelmholtz Zentrum München · DE

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007365 · NIGMS · STANFORD UNIVERSITY · PI CHUA, KATRIN F · 1985 to 2021
$33.8M
Interrogation of individual cells to identify progenitors and their nichesU01HL099999 · NHLBI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2009 to 2015
$7.8M
HOMING RECEPTOR DETERMINANTS ON HSCR01HL058770 · NHLBI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 1998 to 2013
$3.9M
MORPHINE AND ANALOGUES EFFECTS ON CELL METABOLISMR01DA000017 · NIDA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI SIMON, ERIC J · 1985 to 2007
$2.0M
NEW PSYCHOMETRIC METHODS FOR SUBSTANCE ABUSE RESEARCHK05DA000017 · NIDA · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BENTLER, PETER M · 1986 to 2012
$1.3M
Molecular and Cellular Changes in the Peritoneal Surface Mesothelium during Adhesion FormationF30DK108561 · NIDDK · STANFORD UNIVERSITY · PI TSAI, JONATHAN MICHAEL · 2015 to 2018
$96k
NHLBI NIH HHS R01 HL058770NHLBI NIH HHS U01 HL099999NIDA NIH HHS K05 DA000017NIDA NIH HHS R01 DA000017NIDDK NIH HHS F30 DK108561NIGMS NIH HHS T32 GM007365
6 · The paper itself

Abstract

The regeneration of organ morphology and function following tissue loss is critical to restore normal physiology, yet few cases are documented in mammalian postnatal life. Partial hepatectomy of the adult mammalian liver activates compensatory hepatocyte hypertrophy and cell division across remaining lobes, resulting in restitution of organ mass but with permanent alteration of architecture. Here, we identify a time window in early postnatal life wherein partial amputation culminates in a localized regeneration instead of global hypertrophy and proliferation. Quantifications of liver mass, enzymatic activity, and immunohistochemistry demonstrate that damaged lobes underwent multilineage regeneration, reforming a lobe often indistinguishable from undamaged ones. Clonal analysis during regeneration reveals local clonal expansions of hepatocyte stem/progenitors at injured sites that are lineage but not fate restricted. Tetrachimeric mice show clonal selection occurs during development with further selections following injury. Surviving progenitors associate mainly with central veins, in a pattern of selection different from that of normal development. These results illuminate a previously unknown program of liver regeneration after acute injury and allow for exploration of latent regenerative programs with potential applications to adult liver regeneration.

Indexed as

Liver RegenerationAnimalsAnimals, NewbornCell DivisionCell LineageClone CellsLiverMiceModels, BiologicalStem Cellshepatocytelineage-restricted progenitorsliverregenerationstem cells

Identifiers

PMID28330992
PMCPMC5389277
OpenAlexW2602667360

What OpenQuestion holds

Textmetadata
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.