Evidence map›Paper›PMID 33334068›Full record

ArticleInternational journal of molecular sciences2020

Intrinsic Angiogenic Potential and Migration Capacity of Human Mesenchymal Stromal Cells Derived from Menstrual Blood and Bone Marrow.

Rosana de Almeida Santos, Karina Dutra Asensi, Julia Helena Oliveira de Barros, Rafael Campos Silva de Menezes, Ingrid Rosenburg Cordeiro, José Marques de Brito Neto, Tais Hanae Kasai-Brunswick, Regina Coeli Dos Santos Goldenberg

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

10 citing papers in PubMed, 16 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Rosana de Almeida SantosCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.
Karina Dutra AsensiCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.ORCID 0000-0002-8649-3226
Julia Helena Oliveira de BarrosCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.ORCID 0000-0003-3701-1558
Rafael Campos Silva de MenezesCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.
Ingrid Rosenburg CordeiroInstitute of Biomedical Sciences, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.ORCID 0000-0001-9950-9939
José Marques de Brito NetoInstitute of Biomedical Sciences, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.
Tais Hanae Kasai-BrunswickCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.
Regina Coeli Dos Santos GoldenbergCarlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, Rio de Janeiro 21941902, Brazil.ORCID 0000-0002-0886-9603
Universidade Federal do Rio de Janeiro · BRTokyo Institute of Technology · JP

Funding

Lacrimal Gland Repair Using Progenitor CellsR01EY026202 · NEI · SCRIPPS RESEARCH INSTITUTE, THE · PI MAKARENKOVA, HELEN P. · 2016 to 2025
$5.2M
Brazilian Council for Scientific and Technological Development (CNPq) 465656;2014-5National Center of Science and Technology for Regenerative Medicine/REGENERA 465656/2014-5National Research Council/CNPq 401816/2016-8Rio de Janeiro Research State Foundation/FAPERJ E-26/202.963/2017
6 · The paper itself

Abstract

Several therapies are being developed to increase blood circulation in ischemic tissues. Despite bone marrow-derived mesenchymal stromal cells (bmMSC) are still the most studied, an interesting and less invasive MSC source is the menstrual blood, which has shown great angiogenic capabilities. Therefore, the aim of this study was to evaluate the angiogenic properties of menstrual blood-derived mesenchymal stromal cells (mbMSC) in vitro and in vivo and compared to bmMSC. MSC's intrinsic angiogenic capacity was assessed by sprouting and migration assays. mbMSC presented higher invasion and longer sprouts in 3D culture. Additionally, both MSC-spheroids showed cells expressing CD31. mbMSC and bmMSC were able to migrate after scratch wound in vitro, nonetheless, only mbMSC demonstrated ability to engraft in the chick embryo, migrating to perivascular, perineural, and chondrogenic regions. In order to study the paracrine effects, mbMSC and bmMSC conditioned mediums were capable of stimulating HUVEC's tube-like formation and migration. Both cells expressed VEGF-A and FGF2. Meanwhile, PDGF-B was expressed exclusively in mbMSC. Our results indicated that mbMSC and bmMSC presented a promising angiogenic potential. However, mbMSC seems to have additional advantages since it can be obtained by non-invasive procedure and expresses PDGF-B, an important molecule for vascular formation and remodeling.

Indexed as

Cell DifferentiationCell MovementNeovascularization, PhysiologicAnimalsBone Marrow CellsCell ProliferationCells, CulturedChick EmbryoFemaleHumansHuman Umbilical Vein Endothelial CellsImmunohistochemistryMesenchymal Stem Cellsangiogenesisbone marrow mesenchymal stromal cellshuman umbilical vein endothelial cellsmenstrual blood-derived mesenchymal stromal cells

Identifiers

PMID33334068
PMCPMC7765504
OpenAlexW3113364835

What OpenQuestion holds

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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.