Evidence map›Paper›PMID 34693750›Full record

ArticleTissue engineering. Part A2022

A Quick and Efficient Method for the Generation of Immunomodulatory Mesenchymal Stromal Cell from Human Induced Pluripotent Stem Cell.

Michela Bruschi, Neety Sahu, Mamta Singla, Fiorella Grandi, Pranay Agarwal, Constance Chu, Nidhi Bhutani

Open access · greenAbstract read
In one paragraph

Article in Tissue engineering. Part A, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Functionalized 3D scaffolds for engineering the hematopoietic niche.Frontiers in bioengineering and biotechnology · 2022
    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.

Michela BruschiDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Neety SahuDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Mamta SinglaDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Fiorella GrandiDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Pranay AgarwalDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Constance ChuDepartment of Orthopaedic Surgery, PAVAHCS, Palo Alto, California, USA.
Nidhi BhutaniDepartment of Orthopedic Surgery, School of Medicine, Stanford University, Stanford, California, USA.
Gladstone Institutes · US

Funding

Evaluating the Potential of Human Induced Pluripotent Stem Cells (hiPSC) For Cartilage RepairR01AR070864 · NIAMS · STANFORD UNIVERSITY · PI BHUTANI, NIDHI · 2017 to 2021
$2.2M
Targeting DNA Demethylation Regulators in OsteoarthritisR01AR070865 · NIAMS · STANFORD UNIVERSITY · PI BHUTANI, NIDHI · 2016 to 2020
$1.7M
NIAMS NIH HHS R01 AR070864NIAMS NIH HHS R01 AR070865
6 · The paper itself

Abstract

Mesenchymal stromal cells (MSCs) have been widely investigated for their regenerative capacity, anti-inflammatory properties and beneficial immunomodulatory effects across multiple clinical indications. Nevertheless, their widespread clinical utilization is limited by the variability in MSC quality, impacted by donor age, metabolism, and disease. Human induced pluripotent stem cells (hiPSCs) generated from readily accessible donor tissues, are a promising source of stable and rejuvenated MSC but differentiation methods generally require prolonged culture and result in low frequencies of stable MSCs. To overcome this limitation, we have optimized a quick and efficient method for hiPSC differentiation into footprint-free MSCs (human induced MSCs [hiMSCs]) in this study. This method capitalizes on the synergistic action of growth factors Wnt3a and Activin A with bone morphogenetic protein-4 (BMP4), leading to an enrichment of MSC after only 4 days of treatment. These hiMSCs demonstrate a significant upregulation of mesenchymal stromal markers (CD105

Indexed as

Induced Pluripotent Stem CellsMesenchymal Stem CellsCell DifferentiationChondrogenesisHumansImmunomodulationOsteogenesisdifferentiationinduced pluripotent stem cellsmesenchymal stromal cellsosteoarthritisparacrine factorsregenerative medicine

Identifiers

PMID34693750
PMCPMC9131357
OpenAlexW3210043882

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.