Evidence map›Paper›PMID 18085377›Full record

ArticleMedical molecular morphology2007

Neutralization of CXCL10 accelerates liver regeneration in carbon tetrachloride-induced acute liver injury.

Hiroyuki Yoneyama, Yoshiro Kai, Jun Koyama, Kenji Suzuki, Hiroshi Kawachi, Shosaku Narumi, Takafumi Ichida

Abstract read
PubMed Publisher
In one paragraph

Article in Medical molecular morphology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Hiroyuki YoneyamaLaboratory of Stem Cell Dynamism, Stelic Institute of Regenerative Medicine, Stelic Institute & Co., 1-9-15 Higashi-azabu, Mihato-ku, Tokyo, Japan. yoneyama@stelic.co.jp
Yoshiro Kai
Jun Koyama
Kenji Suzuki
Hiroshi Kawachi
Shosaku Narumi
Takafumi Ichida
Stelic Institute (Japan) · JPNiigata University · JPJuntendo University Shizuoka Hospital · JPNara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remodeling of hepatic tissue structure following injury requires the coordinated action of hepatocytes, hepatic stellate cells (HSCs), and endothelial cells. However, their in vivo properties are not fully understood. We report here that the chemokine CXCL10 regulates hepatic tissue remodeling in a carbon tetrachloride (CCl(4))-induced acute liver injury in mice. The production of CXCL10 was enhanced by hepatocytes after CCl(4) exposure. Neutralization of CXCL10 protected mice from acute liver dysfunction and diminished hepatocellular loss. The hepatoprotective effect was associated with increased numbers of 5'-bromo-2' deoxyuridine (BrdU)+ hepatocytes from day 1 and with accumulation of HSCs and endothelial cells within the injured zones from day 3. In vitro, recombinant CXCL10 directly inhibited the proliferation of hepatocytic cells, establishing a novel role of CXCL10 in modulating hepatocyte proliferation, in addition to a previously reported angiostatic role. In summary, neutralization of CXCL10 initially stimulates hepatocyte proliferation and, subsequently, HSC migration and angiogenesis to facilitate remodeling of hepatic cords. Thus, CXCL10 can be a novel therapeutic target for acute hepatocellular damage by regulating liver tissue remodeling.

Indexed as

Liver RegenerationAlanine TransaminaseAnimalsCarbon TetrachlorideCell ProliferationChemokine CXCL10FemaleHepatocytesLiver Failure, AcuteMiceMice, Inbred C57BLNeutralization TestsRecombinant ProteinsRNA, MessengerUp-RegulationAlanine TransaminaseCarbon TetrachlorideChemokine CXCL10Recombinant ProteinsRNA, Messenger

Identifiers

PMID18085377
OpenAlexW2038183080

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.