Evidence map›Paper›PMID 21703205›Full record

ArticleJournal of hepatology2011

Treatment of newborn G6pc(-/-) mice with bone marrow-derived myelomonocytes induces liver repair.

Roberta Resaz, Laura Emionite, Cristina Vanni, Simonetta Astigiano, Maura Puppo, Rosa Lavieri, Daniela Segalerba, Annalisa Pezzolo, Maria Carla Bosco, Alessandra Oberto and 5 more

Open access · greenAbstract read
In one paragraph

Article in Journal of hepatology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Frontiers in pharmacology · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Liver transplantation in glycogen storage disease type I.Orphanet journal of rare diseases · 2014
    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

15 authors at 5 institutions in 2 countries.

Roberta ResazLaboratory of Molecular Biology, G Gaslini Institute, Genova, Italy.
Laura Emionite
Cristina Vanni
Simonetta Astigiano
Maura Puppo
Rosa Lavieri
Daniela Segalerba
Annalisa Pezzolo
Maria Carla Bosco
Alessandra Oberto
Carola Eva
Janice Y Chou
Luigi Varesio
Ottavia Barbieri
Alessandra Eva
Istituto Giannina Gaslini · ITEunice Kennedy Shriver National Institute of Child Health and Human Development · USNeuroscience Institute · ITUniversity of Genoa · ITUniversity of Turin · IT

Funding

Molecular Genetics Of Heritable Human DisordersZIAHD000912 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI CHOU, JANICE · 2009 to 2025
$25.1M
MOLECULAR GENETICS OF HERITABLE HUMAN DISORDERSZ01HD000912 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI CHOU, JANICE · 1985 to 2008
$3.5M
Intramural NIH HHS Z01 HD000912
6 · The paper itself

Abstract

BACKGROUND &

aimsSeveral studies have shown that bone marrow-derived committed myelomonocytic cells can repopulate diseased livers by fusing with host hepatocytes and can restore normal liver function. These data suggest that myelomonocyte transplantation could be a promising approach for targeted and well-tolerated cell therapy aimed at liver regeneration. We sought to determine whether bone marrow-derived myelomonocytic cells could be effective for liver reconstitution in newborn mice knock-out for glucose-6-phosphatase-α.

methodsBone marrow-derived myelomonocytic cells obtained from adult wild type mice were transplanted in newborn knock-out mice. Tissues of control and treated mice were frozen for histochemical analysis, or paraffin-embedded and stained with hematoxylin and eosin for histological examination or analyzed by immunohistochemistry or fluorescent in situ hybridization.

resultsHistological sections of livers of treated knock-out mice revealed areas of regenerating tissue consisting of hepatocytes of normal appearance and partial recovery of normal architecture as early as 1 week after myelomonocytic cells transplant. FISH analysis with X and Y chromosome paints indicated fusion between infused cells and host hepatocytes. Glucose-6-phosphatase activity was detected in treated mice with improved profiles of liver functional parameters.

conclusionsOur data indicate that bone marrow-derived myelomonocytic cell transplant may represent an effective way to achieve liver reconstitution of highly degenerated livers in newborn animals.

Indexed as

AnimalsAnimals, NewbornBone Marrow TransplantationFemaleGlucose-6-PhosphataseGlycogen Storage Disease Type ILiverLiver RegenerationMaleMiceMice, CongenicMice, Inbred C57BLMice, KnockoutMice, TransgenicMyeloid CellsPregnancyGlucose-6-Phosphatase

Identifiers

PMID21703205
PMCPMC6541203
OpenAlexW2011209618

What OpenQuestion holds

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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.