Evidence map›Paper›PMID 30133344›Full record

ArticleMolecular biology of the cell2018

The tetraspanin CD82 regulates bone marrow homing and engraftment of hematopoietic stem and progenitor cells.

Chelsea A Saito-Reis, Kristopher D Marjon, Erica M Pascetti, Muskan Floren, Jennifer M Gillette

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  11. Tetraspanin CD82 regulates S1PRStem cell reports · 2021
    Article
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  14. 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

5 authors.

Chelsea A Saito-ReisDepartment of Pathology, University of New Mexico Health Science Center, University of New Mexico, Albuquerque, NM 87131.
Kristopher D MarjonDepartment of Pathology, University of New Mexico Health Science Center, University of New Mexico, Albuquerque, NM 87131.
Erica M PascettiDepartment of Pathology, University of New Mexico Health Science Center, University of New Mexico, Albuquerque, NM 87131.
Muskan FlorenDepartment of Pathology, University of New Mexico Health Science Center, University of New Mexico, Albuquerque, NM 87131.
Jennifer M GilletteDepartment of Pathology, University of New Mexico Health Science Center, University of New Mexico, Albuquerque, NM 87131.

Funding

WOMEN'S CANCERS RESEARCH PROGRAMP30CA118100 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Yolanda Sanchez · 2005 to 2026
$57.1M
UNM TRAININGP50GM085273 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI LIDKE, KEITH A · 2009 to 2018
$26.1M
UNM PREP (Post-baccalaureate Research Education ProgramR25GM075149 · NIGMS · UNIVERSITY OF NEW MEXICO · PI Kelly Miller · 2005 to 2026
$7.3M
MINORITY INSTITUTIONAL RESEARCH TRAINING PROGRAM (T32)T32HL007736 · NHLBI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI RESTA, THOMAS C · 1993 to 2025
$6.5M
Functional Role of Tetraspanin CD82 in Hematopoietic Stem Cell InteractionsR01HL122483 · NHLBI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jennifer Gillette · 2015 to 2026
$4.2M
The Impact of CD82 Expression on Acute Myeloid Leukemia Chemosensitivity and Disease RelapseF31CA232480 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI FLOREN, MUSKAN · 2018 to 2020
$84k
NCI NIH HHS F31 CA232480NCI NIH HHS P30 CA118100NHLBI NIH HHS R01 HL122483NHLBI NIH HHS T32 HL007736NIGMS NIH HHS P50 GM085273NIGMS NIH HHS R25 GM075149
6 · The paper itself

Abstract

Hematopoietic stem and progenitor cell (HSPC) transplantation represents a treatment option for patients with malignant and nonmalignant hematological diseases. Initial steps in transplantation involve the bone marrow homing and engraftment of peripheral blood-injected HSPCs. In recent work, we identified the tetraspanin CD82 as a potential regulator of HSPC homing to the bone marrow, although its mechanism remains unclear. In the present study, using a CD82 knockout (CD82KO) mouse model, we determined that CD82 modulates HSPC bone marrow maintenance, homing, and engraftment. Bone marrow characterization identified a significant decrease in the number of long-term hematopoietic stem cells in the CD82KO mice, which we linked to cell cycle activation and reduced stem cell quiescence. Additionally, we demonstrate that CD82 deficiency disrupts bone marrow homing and engraftment, with in vitro analysis identifying further defects in migration and cell spreading. Moreover, we find that the CD82KO HSPC homing defect is due at least in part to the hyperactivation of Rac1, as Rac1 inhibition rescues homing capacity. Together, these data provide evidence that CD82 is an important regulator of HSPC bone marrow maintenance, homing, and engraftment and suggest exploiting the CD82 scaffold as a therapeutic target for improved efficacy of stem cell transplants.

Indexed as

AnimalsBone Marrow CellsCell MovementCells, CulturedDisease Models, AnimalFemaleHematopoietic Stem CellsHematopoietic Stem Cell TransplantationKangai-1 ProteinMaleMiceMice, Inbred C57BLMice, KnockoutCd82 antigen, mouseKangai-1 Protein

Identifiers

PMID30133344
PMCPMC6329911

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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.