Evidence map›Paper›PMID 33478018›Full record

ArticleInternational journal of molecular sciences2021

Interactome Analysis of iPSC Secretome and Its Effect on Macrophages In Vitro.

Luca Tamò, Kleanthis Fytianos, Fabienne Caldana, Cedric Simillion, Anis Feki, Izabela Nita, Manfred Heller, Thomas Geiser, Amiq Gazdhar

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
0.6field-weighted citation impact, top 34% 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, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. hiPSC-Derived Cells as Models for Drug Discovery.International journal of molecular sciences · 2021
    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

9 authors at 2 institutions in 1 country.

Luca TamòDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.
Kleanthis FytianosDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.
Fabienne CaldanaDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.
Cedric SimillionDepartment of BioMedical Research, University of Bern, 3008 Bern, Switzerland.
Anis FekiDepartment of Gynecology and Obstetrics, Cantonal Hospital Fribourg, 1702 Fribourg, Switzerland.ORCID 0000-0002-9817-9445
Izabela NitaDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.
Manfred HellerDepartment of BioMedical Research, University of Bern, 3008 Bern, Switzerland.ORCID 0000-0002-6364-7325
Thomas GeiserDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.
Amiq GazdharDepartment of Pulmonary Medicine, University Hospital Bern, 3008 Bern, Switzerland.ORCID 0000-0002-4807-8785
University of Bern · CHFribourg Development Agency · CH

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung CRSII3_160704/1
6 · The paper itself

Abstract

Induced pluripotent stem cell secretome (iPSC-CM) mitigate organ injury and help in repair. Macrophages play a critical role in tissue repair and regeneration and can be directed to promote tissue repair by iPSC-CM, although the exact mechanisms are not known. In the current investigative study, we evaluated the possible mechanism by which iPSC-CM regulates the phenotype and secretory pattern of macrophages in vitro. Macrophages were obtained from human peripheral blood mononuclear cells and differentiated to various subpopulations and treated with either iPSC-CM or control media in vitro. Macrophage phenotype was assessed by flow cytometry, gene expression changes by qRT PCR and secretory pattern by multiplex protein analysis. The protein and gene interaction network revealed the involvement of Amyloid precursor protein (APP) and ELAV-like protein 1 (ELAVL-1) both present in the iPSC-CM to play an important role in regulating the macrophage phenotype and their secretory pattern. This exploratory study reveals, in part, the possible mechanism and identifies two potential targets by which iPSC-CM regulate macrophages and help in repair and regeneration.

Indexed as

ProteomeCell DifferentiationCells, CulturedCulture Media, ConditionedGene Expression ProfilingGene Expression RegulationHumansInduced Pluripotent Stem CellsLeukocytes, MononuclearMacrophagesProtein Interaction MapsCulture Media, ConditionedProteomeinduced pluripotent stem cellslung fibrosislung repair and regenerationmacrophagesstem cells secretome

Identifiers

PMID33478018
PMCPMC7835982
OpenAlexW3122543493

What OpenQuestion 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 OpenQuestion graph.