Evidence map›Paper›PMID 36585572›Full record

ArticleStem cell reviews and reports2023

Whole bone subcutaneous transplantation as a strategy to study precisely the bone marrow niche.

Caroline C Picoli, Patrícia Rocha Martins, Xiao Lin Casey Wong, Thamires Righi, Pedro P G Guimarães, Mauro C X Pinto, Jaime H Amorim, Vasco A C Azevedo, Silma Regina Pereira, Alexandre Kanashiro and 5 more

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Article in Stem cell reviews and reports, 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
1.1field-weighted citation impact, top 20% 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, 7 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

15 authors at 8 institutions in 2 countries.

Caroline C PicoliDepartment of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Patrícia Rocha MartinsDepartment of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Xiao Lin Casey WongDepartment of Dermatology, University of Wisconsin-Madison, Medical Sciences Center, Rm 4385, 1300 University Avenue, Madison, WI, 53706, USA.
Thamires RighiDepartment of Dermatology, University of Wisconsin-Madison, Medical Sciences Center, Rm 4385, 1300 University Avenue, Madison, WI, 53706, USA.
Pedro P G GuimarãesDepartment of Physiology and Biophysics, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Mauro C X PintoInstitute of Biological Sciences, Federal University of Goiás, Goiânia, GO, Brazil.
Jaime H AmorimCenter of Biological Sciences and Health, Federal University of West Bahia, Barreiras, BA, Brazil.
Vasco A C AzevedoDepartment of Genetics, Ecology and Evolution, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Silma Regina PereiraDepartment of Biology, Federal University of Maranhão, São Luís, MA, Brazil.
Alexandre KanashiroDepartment of Dermatology, University of Wisconsin-Madison, Medical Sciences Center, Rm 4385, 1300 University Avenue, Madison, WI, 53706, USA.
Fabio Cardoso CruzDepartment of Pharmacology, Federal University of São Paulo, São Paulo, SP, Brazil.
Rodrigo R ResendeDepartment of Biochemistry and Immunology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Akiva MintzDepartment of Radiology, Columbia University Medical Center, New York, NY, USA.
Paul S FrenetteGottesman Institute for Stem Cell and Regenerative Medicine Research, Albert Einstein College of Medicine, Bronx, New York, NY, USA.
Alexander BirbrairDepartment of Pathology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil. birbrair@wisc.edu.ORCID 0000-0003-1015-2561
Universidade Federal de Minas Gerais · BRUniversity of Wisconsin–Madison · USAlbert Einstein College of Medicine · USColumbia University Irving Medical Center · USUniversidade Federal de Goiás · BRUniversidade Federal de São Paulo · BRUniversidade Federal do Maranhão · BRUniversidade Federal do Oeste da Bahia · BR

Funding

Therapeutically Exploiting a Newly Isolated Neural-Like Stem Cell Against GSBR01CA179072 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MINTZ, AKIVA · 2015 to 2020
$1.6M
NCI NIH HHS R01 CA179072
6 · The paper itself

Abstract

Hematopoietic stem cells are maintained in a specialized microenvironment, known as the 'niche', within the bone marrow. Understanding the contribution of cellular and molecular components within the bone marrow niche for the maintenance of hematopoietic stem cells is crucial for the success of therapeutic applications. So far, the roles of crucial mechanisms within the bone marrow niche have been explored in transgenic animals in which genetic modifications are ubiquitously introduced in the whole body. The lack of precise tools to explore genetic alterations exclusively within the bone marrow prevents our determination of whether the observed outcomes result from confounding effects from other organs. Here, we developed a new method - 'whole bone subcutaneous transplantation'- to study the bone marrow niche in transgenic animals precisely. Using immunolabeling of CD45.1 (donor) vs. CD45.2 (recipient) hematopoeitic stem cells, we demonstrated that hematopoeitic stem cells from the host animals colonize the subcutaneously transplanted femurs after transplantation, while the hematopoietic stem cells from the donor disappear. Strikinlgy, the bone marrow niche of these subcutaneously transplanted femurs remain from the donor mice, enabling us to study specifically cells of the bone marrow niche using this model. We also showed that genetic ablation of peri-arteriolar cells specifically in donor femurs reduced the numbers of hematopoietic stem cells in these bones. This supports the use of this strategy as a model, in combination with genetic tools, to evaluate how bone marrow niche specific modifications may impact non-modified hematopoietic stem cells. Thus, this approach can be utilized for genetic manipulation in vivo of specific cell types only within the bone marrow. The combination of whole bone subcutaneous transplantation with rodent transgenic models will facilitate a more precise, complex and comprehensive understanding of existing problems in the study of the hematopoietic stem cell bone marrow niche.

Indexed as

Bone MarrowHematopoietic Stem Cell TransplantationAnimalsBone and BonesBone Marrow TransplantationHematopoietic Stem CellsMiceBoneCre/loxp systemFemurMouse modelNicheStem cellsTransplantation

Identifiers

PMID36585572
OpenAlexW4313340518

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.