Evidence map›Paper›PMID 37864264›Full record

ArticleStem cell research & therapy2023

Platelet-derived circulating soluble P-selectin is sufficient to induce hematopoietic stem cell mobilization.

Tso-Fu Wang, Yu-Shan Liou, Shang-Hsien Yang, Guan-Ling Lin, Ya-Wen Chiang, Te-Sheng Lien, Chi-Cheng Li, Jen-Hung Wang, Hsin-Hou Chang, Der-Shan Sun

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

10 authors at 3 institutions in 2 countries.

Tso-Fu Wang *Department of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China.
Yu-Shan Liou *Department of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China.
Shang-Hsien YangDepartment of Medicine, College of Medicine, Tzu Chi University, Hualien, Taiwan, Republic of China.
Guan-Ling LinDepartment of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China.
Ya-Wen ChiangDepartment of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China.
Te-Sheng LienDepartment of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China.
Chi-Cheng LiDepartment of Hematology and Oncology, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China.
Jen-Hung WangDepartment of Medical Research, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien, Taiwan, Republic of China.
Hsin-Hou ChangDepartment of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China. hhchang@mail.tcu.edu.tw.
Der-Shan SunDepartment of Molecular Biology and Human Genetics, College of Medicine, Tzu Chi University, No. 701, Section 3, Zhong-Yang Road, Hualien, 97004, Taiwan, Republic of China. dssun@mail.tcu.edu.tw.ORCID 0000-0002-1994-7355
Tzu Chi University · TWHualien Tzu Chi Medical Center · TWTzu Chi Foundation · TW

Funding

Buddhist Tzu Chi Medical Foundation TCMMP104-06Buddhist Tzu Chi Medical Foundation TCMMP108-04Buddhist Tzu Chi Medical Foundation TCMMP111-01Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCAS-112-02Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCRD106-42Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCRD108-55Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCRD110-61Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCRD111-082Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation TCRD112-054Ministry of Science and Technology, Taiwan MOST103-2321-B-320-001Ministry of Science and Technology, Taiwan MOST105-2633-B-320-001Ministry of Science and Technology, Taiwan MOST106-2633-B-320-001Ministry of Science and Technology, Taiwan MOST108-2311-B-320-001
6 · The paper itself

Abstract

backgroundGranulocyte colony-stimulating factor (G-CSF)-mediated mobilization of hematopoietic stem cells (HSCs) is a well-established method to prepare HSCs for transplantation nowadays. A sufficient number of HSCs is critical for successful HSC transplantation. However, approximately 2-6% of healthy stem cell donors are G-CSF-poor mobilizers for unknown reasons; thus increasing the uncertainties of HSC transplantation. The mechanism underlining G-CSF-mediated HSC mobilization remains elusive, so detailed mechanisms and an enhanced HSC mobilization strategy are urgently needed. Evidence suggests that P-selectin and P-selectin glycoprotein ligand-1 (PSGL-1) are one of the cell-cell adhesion ligand-receptor pairs for HSCs to keep contacting bone marrow (BM) stromal cells before being mobilized into circulation. This study hypothesized that blockage of PSGL-1 and P-selectin may disrupt HSC-stromal cell interaction and facilitate HSC mobilization.

methodsThe plasma levels of soluble P-selectin (sP-sel) before and after G-CSF administration in humans and male C57BL/6J mice were analyzed using enzyme-linked immunosorbent assay. Male mice with P-selectin deficiency (Selp

resultsA significant increase in plasma sP-sel levels was observed in humans and mice following G-CSF administration. Treatments of G-CSF induced a decrease in the level of HSC mobilization in Selp

conclusionssP-sel was identified as a novel endogenous HSC-mobilizing agent. sP-sel injections achieved a relatively faster and more convenient regimen to mobilize HSCs in mice than G-CSF. These findings may serve as a reference for developing and optimizing human HSC mobilization in the future.

Indexed as

Hematopoietic Stem Cell MobilizationP-SelectinAnimalsGranulocyte Colony-Stimulating FactorHematopoietic Stem CellsHumansMaleMiceMice, Inbred C57BLRecombinant ProteinsGranulocyte Colony-Stimulating FactorP-SelectinRecombinant ProteinsGranulocyte colony-stimulating factorHematopoietic stem cell mobilizationSoluble P-selectin

Identifiers

PMID37864264
PMCPMC10589967
OpenAlexW4387823671

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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.