Evidence map›Paper›PMID 35582777›Full record

ArticleCell proliferation2022

Hoxb5 reprogrammes murine multipotent blood progenitors into haematopoietic stem cell-like cells.

Dehao Huang, Qianhao Zhao, Mengyun Zhang, Qitong Weng, Qi Zhang, Kaitao Wang, Fang Dong, Hui Cheng, Fangxiao Hu, Jinyong Wang

Open access · goldAbstract read
In one paragraph

Article in Cell proliferation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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 4 institutions in 1 country.

Dehao HuangCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Qianhao ZhaoFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, China.
Mengyun ZhangGMU-GIBH Joint School of Life Sciences, Guangzhou Medical University, Guangzhou, China.
Qitong WengCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Qi ZhangCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Kaitao WangSchool of Biomedical Engineering, Sun Yat-Sen University, Shenzhen, China.
Fang DongState Key Laboratory of Experimental Hematology & National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Hui ChengState Key Laboratory of Experimental Hematology & National Clinical Research Center for Blood Diseases, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, China.
Fangxiao HuCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
Jinyong WangCAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.ORCID https://orcid.org/0000-0002-7218-0659
Chinese Academy of Sciences · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNSun Yat-sen University · CNGuangzhou Medical University · CN

Funding

National Natural Science Foundation of China 31900816National Natural Science Foundation of China 81925002National Natural Science Foundation of China 82100127the Frontier Science Research Program of the CAS QYZDB-SSW-SMC057
6 · The paper itself

Abstract

objectivesThe expression of transcription factor Hoxb5 specifically marks the functional haematopoietic stem cells (HSC) in mice. However, our recent work demonstrated that ectopic expression of Hoxb5 exerted little effect on HSC but could convert B-cell progenitors into functional T cells in vivo. Thus, cell type- and development stage-specific roles of Hoxb5 in haematopoietic hierarchy await more extensive exploration. In this study, we aim to investigate the effect of Hoxb5 expression in multipotent blood progenitor cells. MATERIALS AND

methodsA Mx1cre/Rosa

resultsHere, with a mouse strain engineered with conditional expression of Hoxb5, we unveiled that induced expression of Hoxb5 in MPP led to the generation of a de novo Sca1

conclusionsOur current study uncovers that Hoxb5 can empower MPP with self-renewal ability and indicates an alternative approach for generating HSC-like cells in vivo from blood lineage cells.

Indexed as

HematopoiesisHematopoietic Stem CellsAnimalsCell DifferentiationGene Expression RegulationHomeodomain ProteinsMiceMice, Inbred C57BLMultipotent Stem CellsHomeodomain ProteinsHoxb5 protein, mouse

Identifiers

PMID35582777
PMCPMC9201374
OpenAlexW4280617406

What OpenQuestion holds

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LicenceCC BY
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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.