Evidence map›Paper›PMID 35023637›Full record

ReviewAdvanced biology2022

The Molecular Mechanisms Through Which Placental Mesenchymal Stem Cell-Derived Extracellular Vesicles Promote Myelin Regeneration.

Kaitlin C Clark, David Wang, Priyadarsini Kumar, Sirjan Mor, Edwin Kulubya, Sabrina V Lazar, Aijun Wang

Open access · greenAbstract readReview
In one paragraph

Review in Advanced biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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 1 institution in 1 country.

Kaitlin C ClarkUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.
David WangUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.
Priyadarsini KumarUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.
Sirjan MorUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.
Edwin KulubyaUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.
Sabrina V LazarUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.ORCID 0000-0001-6359-2611
Aijun WangUC Davis Health: Department of Surgery, 4625 2nd Ave., Research II, Room 3101, Sacramento, CA, 95817, USA.ORCID 0000-0002-2985-3627
UC Davis Health · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
UC Davis Alzheimer's Disease Core CenterP30AG010129 · NIA · UNIVERSITY OF CALIFORNIA DAVIS · PI DECARLI, CHARLES · 1991 to 2020
$28.3M
UC Davis CTSC TL1 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility MentorshipTL1TR001861 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI MEDICI, VALENTINA · 2016 to 2025
$4.7M
Engineered Neuroprotective Stem-Cell Exosomes for In Utero Spina Bifida TherapyR01NS115860 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FARMER, DIANA LEE, WANG, AIJUN · 2020 to 2024
$2.5M
Fetal Tissue Engineering to Treat Spina Bifida Before BirthR01NS100761 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WANG, AIJUN · 2017 to 2021
$1.7M
NCATS NIH HHS TL1 TR001861NCATS NIH HHS UL1 TR001860NIA NIH HHS P30 AG010129NINDS NIH HHS R01 NS100761NINDS NIH HHS R01 NS115860
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a debilitating degenerative disease characterized by an immunological attack on the myelin sheath leading to demyelination and axon degeneration. Mesenchymal stem/stromal cells (MSCs) and secreted extracellular vesicles (EVs) have become attractive targets as therapies to treat neurodegenerative diseases such as MS due to their potent immunomodulatory and regenerative properties. The placenta is a unique source of MSCs (PMSCs), demonstrates "fetomaternal" tolerance during pregnancy, and serves as a novel source of MSCs for the treatment of neurodegenerative diseases. PMSCs and PMSC-EVs have been shown to promote remyelination in animal models of MS, however, the molecular mechanisms by which modulation of autoimmunity and promotion of myelination occurs have not been well elucidated. The current review will address the molecular mechanisms by which PMSC-EVs can promote remyelination in MS.

Indexed as

Extracellular VesiclesMesenchymal Stem CellsMultiple SclerosisRemyelinationAnimalsFemaleMyelin SheathPlacentaPregnancyautoimmunityextracellular vesiclemesenchymal stromal cellmultiple sclerosismyelin regenerationplacenta

Identifiers

PMID35023637
PMCPMC9225676
OpenAlexW4206014564

What OpenQuestion holds

Textmetadata
LicenceTDM
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.