Evidence map›Paper›PMID 24599546›Full record

ArticleBlood2014

Expansion of the neonatal platelet mass is achieved via an extension of platelet lifespan.

Zhi-Jian Liu, Karin M Hoffmeister, Zhongbo Hu, Donald E Mager, Sihem Ait-Oudhia, Marlyse A Debrincat, Irina Pleines, Emma C Josefsson, Benjamin T Kile, Joseph Italiano and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
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  4. Investigation of thePharmaceuticals (Basel, Switzerland) · 2025
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  5. DUT (p.Y116C)-Mutation-Induced Thrombocytopenia in Rabbits.International journal of molecular sciences · 2025
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  6. Article
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  14. Platelets in the neonate: Not just a small adult.Research and practice in thrombosis and haemostasis · 2022
    Article
  15. Review
  16. Generation and manipulation of human iPSC-derived platelets.Cellular and molecular life sciences : CMLS · 2021
    Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 7 institutions in 2 countries.

Zhi-Jian LiuDivision of Newborn Medicine, Boston Children's Hospital, Boston, MA;
Karin M HoffmeisterDivision of Translational Medicine, Brigham and Women's Hospital, Boston, MA;
Zhongbo HuDivision of Neonatology, University of Florida, Gainesville, FL;
Donald E MagerDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Buffalo, NY;
Sihem Ait-OudhiaDepartment of Pharmaceutical Sciences, University at Buffalo, State University of New York, Buffalo, NY;
Marlyse A DebrincatCancer and Hematology Division, The Walter and Eliza Hall Institute of Medical Research, and the Department of Medical Biology, University of Melbourne, Parkville, Australia;
Irina PleinesCancer and Hematology Division, The Walter and Eliza Hall Institute of Medical Research, and the Department of Medical Biology, University of Melbourne, Parkville, Australia;
Emma C JosefssonCancer and Hematology Division, The Walter and Eliza Hall Institute of Medical Research, and the Department of Medical Biology, University of Melbourne, Parkville, Australia;
Benjamin T KileCancer and Hematology Division, The Walter and Eliza Hall Institute of Medical Research, and the Department of Medical Biology, University of Melbourne, Parkville, Australia;
Joseph ItalianoDivision of Translational Medicine, Brigham and Women's Hospital, Boston, MA; Division of Hematology, Brigham and Women's Hospital and the Vascular Biology Program, Boston Children's Hospital, Boston, MA; and.
Haley RamseyDivision of Newborn Medicine, Boston Children's Hospital, Boston, MA;
Renata GrozovskyDivision of Translational Medicine, Brigham and Women's Hospital, Boston, MA;
Peter Veng-PedersenCollege of Pharmacy, University of Iowa, Iowa City, IA.
Chaitanya ChavdaDivision of Newborn Medicine, Boston Children's Hospital, Boston, MA;
Martha Sola-VisnerDivision of Newborn Medicine, Boston Children's Hospital, Boston, MA;
Boston Children's Hospital · USBrigham and Women's Hospital · USUniversity at Buffalo, State University of New York · USUniversity of Melbourne · AUWalter and Eliza Hall Institute of Medical Research · AUUniversity of Florida · USUniversity of Iowa · US

Funding

THE RoLE OF NEONATAL ANEMIA IN LEARNING AND MEMORYP01HL046925 · NHLBI · UNIVERSITY OF IOWA · PI JOSEPHSON, CASSANDRA D · 1992 to 2022
$34.3M
REGULATION OF LACTOSAMINYL GLYCAN BIOSYNTHESIS IN HEMATOPOIETIC CELLSP01HL107146 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKSTEIN, ROBERT · 2011 to 2017
$17.7M
Carbohydrate-Mediated Platelet ClearanceR01HL089224 · NHLBI · VERSITI WISCONSIN, INC. · PI Karin Maria Hoffmeister · 2007 to 2026
$9.3M
Cytoskeletal Mechanisms of Platelet FormationR01HL068130 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI ITALIANO, JOSEPH E · 2001 to 2021
$8.1M
Prolonged and Severe Thrombocytopenia in NeonatesR01HL069990 · NHLBI · UNIVERSITY OF FLORIDA · PI SOLA-VISNER, MARTHA C. · 2002 to 2015
$2.8M
NHLBI NIH HHS HL089224NHLBI NIH HHS HL107146NHLBI NIH HHS P01 HL046925NHLBI NIH HHS P01 HL107146NHLBI NIH HHS R01 HL068130NHLBI NIH HHS R01 HL069990NHLBI NIH HHS R01 HL089224
6 · The paper itself

Abstract

The fetal/neonatal hematopoietic system must generate enough blood cells to meet the demands of rapid growth. This unique challenge might underlie the high incidence of thrombocytopenia among preterm neonates. In this study, neonatal platelet production and turnover were investigated in newborn mice. Based on a combination of blood volume expansion and increasing platelet counts, the platelet mass increased sevenfold during the first 2 weeks of murine life, a time during which thrombopoiesis shifted from liver to bone marrow. Studies applying in vivo biotinylation and mathematical modeling showed that newborn and adult mice had similar platelet production rates, but neonatal platelets survived 1 day longer in circulation. This prolonged lifespan fully accounted for the rise in platelet counts observed during the second week of murine postnatal life. A study of pro-apoptotic and anti-apoptotic Bcl-2 family proteins showed that neonatal platelets had higher levels of the anti-apoptotic protein Bcl-2 and were more resistant to apoptosis induced by the Bcl-2/Bcl-xL inhibitor ABT-737 than adult platelets. However, genetic ablation or pharmacologic inhibition of Bcl-2 alone did not shorten neonatal platelet survival or reduce platelet counts in newborn mice, indicating the existence of redundant or alternative mechanisms mediating the prolonged lifespan of neonatal platelets.

Indexed as

Platelet CountAnimalsAnimals, NewbornApoptosisBiphenyl CompoundsBlood PlateletsCell SurvivalHumansInfant, NewbornLiverMean Platelet VolumeMegakaryocytesMiceNitrophenolsPiperazinesProto-Oncogene Proteins c-bcl-2ABT-737Biphenyl CompoundsNitrophenolsPiperazinesProto-Oncogene Proteins c-bcl-2Sulfonamides

Identifiers

PMID24599546
PMCPMC4041172
OpenAlexW1973129306

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.