Evidence map›Paper›PMID 34098576›Full record

ArticleBlood2021

EpoR-tdTomato-Cre mice enable identification of EpoR expression in subsets of tissue macrophages and hematopoietic cells.

Huan Zhang, Shihui Wang, Donghao Liu, Chengjie Gao, Yongshuai Han, Xinhua Guo, Xiaoli Qu, Wei Li, Shijie Zhang, Jingyu Geng and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 35 citations in OpenAlex.

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  10. Macrophages in Hematopoiesis and Related Blood Diseases.Genomics, proteomics & bioinformatics · 2025
    Review
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  12. Review
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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

15 authors at 3 institutions in 3 countries.

Huan ZhangSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Shihui WangSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Donghao LiuSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Chengjie GaoLaboratory of Membrane Biology and.
Yongshuai HanLaboratory of Membrane Biology and.
Xinhua GuoLaboratory of Membrane Biology and.
Xiaoli QuSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Wei LiLaboratory of Membrane Biology and.
Shijie ZhangSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Jingyu GengSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Linlin ZhangSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.
Avital MendelsonLaboratory of Complement Biology, New York Blood Center, New York, NY.ORCID 0000-0002-1120-9593
Karina YazdanbakhshLaboratory of Complement Biology, New York Blood Center, New York, NY.
Lixiang ChenSchool of Life Sciences, Zhengzhou University, Zhengzhou, China; and.ORCID 0000-0001-7785-2496
Xiuli AnLaboratory of Membrane Biology and.
Zhengzhou University · CNLaboratoire de Biologie Physico-Chimique des Protéines Membranaires · FRNew York Blood Center · US

Funding

Sickle cell bone marrow niche and regulation of platelet activation and erythropoiesisP01HL149626 · NHLBI · NEW YORK BLOOD CENTER · PI Karina Yazdanbakhsh · 2020 to 2026
$24.4M
Use of forward Genetic approaches to identify Babesia receptorsR01HL140625 · NHLBI · NEW YORK BLOOD CENTER · PI AN, XIULI, LOBO, CHERYL ANN · 2018 to 2021
$2.8M
NHLBI NIH HHS P01 HL149626NHLBI NIH HHS R01 HL140625
6 · The paper itself

Abstract

The erythropoietin receptor (EpoR) has traditionally been thought of as an erythroid-specific gene. Notably, accumulating evidence suggests that EpoR is expressed well beyond erythroid cells. However, the expression of EpoR in non-erythroid cells has been controversial. In this study, we generated EpoR-tdTomato-Cre mice and used them to examine the expression of EpoR in tissue macrophages and hematopoietic cells. We show that in marked contrast to the previously available EpoR-eGFPcre mice, in which a very weak eGFP signal was detected in erythroid cells, tdTomato was readily detectable in both fetal liver (FL) and bone marrow (BM) erythroid cells at all developmental stages and exhibited dynamic changes during erythropoiesis. Consistent with our recent finding that erythroblastic island (EBI) macrophages are characterized by the expression of EpoR, tdTomato was readily detected in both FL and BM EBI macrophages. Moreover, tdTomato was also detected in subsets of hematopoietic stem cells, progenitors, megakaryocytes, and B cells in BM as well as in spleen red pulp macrophages and liver Kupffer cells. The expression of EpoR was further shown by the EpoR-tdTomato-Cre-mediated excision of the floxed STOP sequence. Importantly, EPO injection selectively promoted proliferation of the EpoR-expressing cells and induced erythroid lineage bias during hematopoiesis. Our findings imply broad roles for EPO/EpoR in hematopoiesis that warrant further investigation. The EpoR-tdTomato-Cre mouse line provides a powerful tool to facilitate future studies on EpoR expression and regulation in various non-hematopoietic cells and to conditionally manipulate gene expression in EpoR-expressing cells for functional studies.

Indexed as

Gene ExpressionAnimalsHematopoietic Stem CellsHumansIntegrasesLuminescent AgentsLuminescent ProteinsMacrophagesMiceReceptors, ErythropoietinRed Fluorescent ProteinCre recombinaseIntegrasesLuminescent AgentsLuminescent ProteinsReceptors, ErythropoietinRed Fluorescent Protein

Identifiers

PMID34098576
PMCPMC8767788
OpenAlexW3172881653

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.