Evidence map›Paper›PMID 37039946›Full record

ArticleStem cell reviews and reports2023

Gingiva-derived Stromal Cells Isolated from Cats Affected with Tooth Resorption Exhibit Increased Apoptosis, Inflammation, and Oxidative Stress while Experiencing Deteriorated Expansion and Anti-Oxidative Defense.

Maria Soltero-Rivera, Sylwia Groborz, Maciej Janeczek, Justyna Kornicka, Monika Wierzgon, Boaz Arzi, Krzysztof Marycz

Open access · greenAbstract read
PubMed Publisher
In one paragraph

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
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

7 authors at 4 institutions in 2 countries.

Maria Soltero-RiveraVeterinary Surgical and Radiological Sciences, University of California, One Shields Avenue, Davis, CA, 95616, USA.
Sylwia GroborzInternational Institute of Translational Medicine (MIMT), Jesionowa 16 Str, 55-114, Wisznia Mala, Poland.
Maciej JaneczekDepartment of Biostructure and Animal Physiology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Kozuchowska 1/3, 51-631, Wrocław, Poland.
Justyna KornickaInternational Institute of Translational Medicine (MIMT), Jesionowa 16 Str, 55-114, Wisznia Mala, Poland.
Monika WierzgonDepartment of Biostructure and Animal Physiology, Faculty of Veterinary Medicine, Wrocław University of Environmental and Life Sciences, Kozuchowska 1/3, 51-631, Wrocław, Poland.
Boaz ArziVeterinary Surgical and Radiological Sciences, University of California, One Shields Avenue, Davis, CA, 95616, USA.
Krzysztof MaryczVeterinary Surgical and Radiological Sciences, University of California, One Shields Avenue, Davis, CA, 95616, USA. kmmarycz@ucdavis.edu.ORCID http://orcid.org/0000-0003-3676-796X
Wrocław University of Environmental and Life Sciences · PLUniversity of California, Davis · USVeterinary Medical Teaching Hospital · USWrocław University of Science and Technology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gingiva-derived mesenchymal stromal cells (GMSCs) are multipotent cells characterized by multilineage differentiation potential, proliferative expansion, and unique immunomodulatory ability, making them attractive as a new treatment of periodontal regeneration. In this study, GMSCs obtained from the gingiva of healthy cats (HE) as well as from cats affected by tooth resorption (TR) were isolated and characterized. Feline GMSCs (fGMSCs) from HE patients exhibited fibroblast-like morphology, developed cellular body, specific growth pattern, high expansion, and proliferative potential as well as reduced senescence signature. fGMSCs demonstrated high s-100 and IL-10 positive cells, while simultaneously having low activity of IL-1. Moreover, high activity of ki-67 combined with reduced senescence markers were noted. In comparison, GMSCs from cats with TR exhibited enlarged nuclei and flat, irregular shape along with increased expression of CD44, s-100 and CD45 and downregulation of CD73. GMSCs from TR cats showed lower ability to form colonies, increased incidence of apoptosis, higher number of senescent cells, and reduced cell migration. Upregulation of pro-inflammatory cytokines was also noted in the TR group along with lower expression of mTOR and miR-17 and upregulation of miR-378. Mitochondrial dynamics, biogenesis and antioxidant properties are also negatively impacted in this group. Collectively, our findings suggest that GMSCs isolated from the gingiva of cats affected with TR have deteriorated functionality caused by impaired proliferation and growth and possibly mediated via mitochondrial dysfunction. fGMSCs or their EV's should be further investigated for their role in the pathophysiology of TR in cats.

Indexed as

Mesenchymal Stem CellsMicroRNAsAnimalsApoptosisCatsGingivaInflammationOxidative StressMicroRNAsFeline gingivostomatitisFeline oral disordersFeline stem cells

Identifiers

PMID37039946
OpenAlexW4364353749

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.