Evidence map›Paper›PMID 29694335›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2018

MYSM1 Is Essential for Maintaining Hematopoietic Stem Cell (HSC) Quiescence and Survival.

Yi Huo, Bing-Yi Li, Zhi-Feng Lin, Wei Wang, Xiao-Xia Jiang, Xu Chen, Wen-Jin Xi, An-Gang Yang, Si-Yi Chen, Tao Wang

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Stem cell transplantation therapy for diabetic foot ulcer: a narrative review.Asian biomedicine : research, reviews and news · 2021
    Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Development of anFuture science OA · 2019
    Article
  12. 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

10 authors at 2 institutions in 2 countries.

Yi HuoState Key Laboratory of Cancer Biology, Department of Medical Genetics and Developmental Biology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Bing-Yi LiUndergraduate Student at Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Zhi-Feng LinUndergraduate Student at Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Wei WangDepartment of Immunology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Xiao-Xia JiangDepartment of Molecular Microbiology and Immunology, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Xu ChenDepartment of Immunology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Wen-Jin XiDepartment of Immunology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
An-Gang YangDepartment of Immunology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Si-Yi ChenDepartment of Molecular Microbiology and Immunology, Norris Comprehensive Cancer Center, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
Tao WangState Key Laboratory of Cancer Biology, Department of Medical Genetics and Developmental Biology, Fourth Military Medical University, Xi'an, Shaanxi, China (mainland).
Air Force Medical University · CNUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND Histone H2A deubiquitinase MYSM1 has recently been shown to be essential for hematopoiesis and hematopoietic stem cell (HSC) function in both mice and humans. However, conventional MYSM1 knockouts cause partial embryonic lethality and growth retardation, and it is difficult to convincingly remove the effects of environmental factors on HSC differentiation and function. MATERIAL AND METHODS MYSM1 conditional knockout (cKO) mice were efficiently induced by using the Vav1-cre transgenic system. The Vav-Cre MYSM1 cKO mice were then analyzed to verify the intrinsic role of MYSM1 in hematopoietic cells. RESULTS MYSM1 cKO mice were viable and were born at normal litter sizes. At steady state, we observed a defect in hematopoiesis, including reduced bone marrow cellularity and abnormal HSC function. MYSM1 deletion drives HSCs from quiescence into rapid cycling, and MYSM1-deficient HSCs display impaired engraftment. In particular, the immature cycling cKO HSCs have elevated reactive oxygen species (ROS) levels and are prone to apoptosis, resulting in the exhaustion of the stem cell pool during stress response to 5-FU. CONCLUSIONS Our study using MYSM1 cKO mice confirms the important role of MYSM1 in maintaining HSC quiescence and survival.

Indexed as

AnimalsApoptosisCell DifferentiationCell DivisionCell SurvivalEndopeptidasesHematopoiesisHematopoietic Stem CellsMiceMice, Inbred C57BLMice, KnockoutReactive Oxygen SpeciesTrans-ActivatorsUbiquitin-Specific ProteasesEndopeptidasesMYSM1 protein, mouseReactive Oxygen SpeciesTrans-ActivatorsUbiquitin-Specific Proteases

Identifiers

PMID29694335
PMCPMC5939948
OpenAlexW2801256290

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.