Evidence map›Paper›PMID 38451606›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2024

Stimulation of mouse hematopoietic stem cells by angiogenin and DNA preparations.

E A Potter, E V Dolgova, A S Proskurina, V S Ruzanova, Y R Efremov, S S Kirikovich, S G Oshikhmina, A L Mamaev, O S Taranov, A S Bryukhovetskiy and 5 more

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.4field-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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 6 institutions in 1 country.

E A PotterInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0003-1558-8655
E V DolgovaInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-5543-248X
A S ProskurinaInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-7650-4331
V S RuzanovaInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-6836-5618
Y R EfremovInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-0649-7543
S S KirikovichInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-3426-4501
S G OshikhminaDepartment of Natural Sciences, Novosibirsk National Research State University, Novosibirsk, Russia.ORCID http://orcid.org/0009-0002-6432-1762
A L MamaevLLC "Angiopharm Laboratory", Novosibirsk, Russia.ORCID http://orcid.org/0009-0007-6727-1576
O S TaranovState Research Center of Virology and Biotechnology "Vector", Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-6746-8092
A S BryukhovetskiyClinical Hospital "Neurovita", Moscow, Russia.ORCID http://orcid.org/0000-0002-3141-1529
L U GrivtsovaDepartment of Clinical Immunology, National Medical Research Radiological Centre, Ministry of Health of the Russian Federation, Obninsk, Russia.ORCID http://orcid.org/0000-0001-9103-9688
N A KolchanovInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0001-6800-8787
A A OstaninResearch Institute of Fundamental and Clinical Immunology, Novosibirsk, Russia.ORCID http://orcid.org/0000-0001-6895-938X
E R ChernykhResearch Institute of Fundamental and Clinical Immunology, Novosibirsk, Russia.ORCID http://orcid.org/0000-0003-2346-6279
S S BogachevInstitute of Cytology and Genetics of the Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia.ORCID http://orcid.org/0000-0002-2019-9382
Institute of Cytology and Genetics · RUResearch Institute of Fundamental and Clinical Immunology · RUMinistry of Health of the Russian Federation · RUNeuroVita Clinic · RUNovosibirsk State University · RUState Research Center of Virology and Biotechnology VECTOR · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immature hematopoietic progenitors are a constant source for renewal of hemocyte populations and the basic component of the tissue and cell repair apparatus. A unique property of these cells of internalizing extracellular double-stranded DNA has been previously shown. The leukostimulatory effect demonstrated in our pioneering studies was considered to be due to the feature of this cell. In the present research, we have analyzed the effects of DNA genome reconstructor preparation (DNAgr), DNAmix, and human recombinant angiogenin on both hematopoietic stem cells and multipotent progenitors. Treatment with bone marrow cells of experimental mice with these preparations stimulates colony formation by hematopoietic stem cells and proliferation of multipotent descendants. The main lineage responsible for this is the granulocyte-macrophage hematopoietic lineage. Using fluorescent microscopy as well as FACS assay, co-localization of primitive c-Kit- and Sca-1-positive progenitors and the TAMRA-labeled double-stranded DNA has been shown. Human recombinant angiogenin was used as a reference agent. Cells with specific markers were quantified in intact bone marrow and colonies grown in the presence of inducers. Quantitative analysis revealed that a total of 14,000 fragment copies of 500 bp, which is 0.2% of the haploid genome, can be delivered into early progenitors. Extracellular double-stranded DNA fragments stimulated the colony formation in early hematopoietic progenitors from the bone marrow, which assumed their effect on cells in G0. The observed number of Sca1+/c-Kit+ cells in colonies testifies to the possibility of both symmetrical and asymmetrical division of the initial hematopoietic stem cell and its progeny.

Indexed as

Hematopoietic Stem CellsRibonuclease, PancreaticAnimalsBone Marrow CellsDNAHumansMiceangiogeninDNARibonuclease, Pancreatic

Identifiers

PMID38451606
PMCPMC10913394
OpenAlexW4392403450

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.