Evidence map›Paper›PMID 38926793›Full record

ReviewStem cell research & therapy2024

iPSCs chondrogenic differentiation for personalized regenerative medicine: a literature review.

Eltahir Abdelrazig Mohamed Ali, Rana Smaida, Morgane Meyer, Wenxin Ou, Zongjin Li, Zhongchao Han, Nadia Benkirane-Jessel, Jacques Eric Gottenberg, Guoqiang Hua

Abstract readReview
In one paragraph

Review in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
–field-weighted citation impact
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

16 citing papers in PubMed.

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  16. 3D Culture of MSCs for Clinical Application.Bioengineering (Basel, Switzerland) · 2024
    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

9 authors.

Eltahir Abdelrazig Mohamed Ali *Institut National de la Santé et de la Recherche Médicale (INSERM), UMR 1260, Regenerative NanoMedicine (RNM), 1 Rue Eugène Boeckel, 67000, Strasbourg, France.
Rana SmaidaLamina Therapeutics, 1 Rue Eugène Boeckel, 67000, Strasbourg, France.
Morgane MeyerUniversité de Strasbourg, 67000, Strasbourg, France.
Wenxin Ou *Université de Strasbourg, 67000, Strasbourg, France.
Zongjin LiNankai University School of Medicine, Tianjin, 300071, China.
Zhongchao HanBeijing Engineering Laboratory of Perinatal Stem Cells, Beijing Institute of Health and Stem Cells, Health & Biotech Co, Beijing, 100176, China.
Nadia Benkirane-JesselInstitut National de la Santé et de la Recherche Médicale (INSERM), UMR 1260, Regenerative NanoMedicine (RNM), 1 Rue Eugène Boeckel, 67000, Strasbourg, France. nadia.jessel@inserm.fr.
Jacques Eric GottenbergUniversité de Strasbourg, 67000, Strasbourg, France. jacques-eric.gottenberg@chru-strasbourg.fr.
Guoqiang HuaInstitut National de la Santé et de la Recherche Médicale (INSERM), UMR 1260, Regenerative NanoMedicine (RNM), 1 Rue Eugène Boeckel, 67000, Strasbourg, France. g.hua@unistra.fr.ORCID 0000-0001-7639-5908

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cartilage, an important connective tissue, provides structural support to other body tissues, and serves as a cushion against impacts throughout the body. Found at the end of the bones, cartilage decreases friction and averts bone-on-bone contact during joint movement. Therefore, defects of cartilage can result from natural wear and tear, or from traumatic events, such as injuries or sudden changes in direction during sports activities. Overtime, these cartilage defects which do not always produce immediate symptoms, could lead to severe clinical pathologies. The emergence of induced pluripotent stem cells (iPSCs) has revolutionized the field of regenerative medicine, providing a promising platform for generating various cell types for therapeutic applications. Thus, chondrocytes differentiated from iPSCs become a promising avenue for non-invasive clinical interventions for cartilage injuries and diseases. In this review, we aim to highlight the current strategies used for in vitro chondrogenic differentiation of iPSCs and to explore their multifaceted applications in disease modeling, drug screening, and personalized regenerative medicine. Achieving abundant functional iPSC-derived chondrocytes requires optimization of culture conditions, incorporating specific growth factors, and precise temporal control. Continual improvements in differentiation methods and integration of emerging genome editing, organoids, and 3D bioprinting technologies will enhance the translational applications of iPSC-derived chondrocytes. Finally, to unlock the benefits for patients suffering from cartilage diseases through iPSCs-derived technologies in chondrogenesis, automatic cell therapy manufacturing systems will not only reduce human intervention and ensure sterile processes within isolator-like platforms to minimize contamination risks, but also provide customized production processes with enhanced scalability and efficiency.

Indexed as

Cell DifferentiationChondrogenesisInduced Pluripotent Stem CellsPrecision MedicineRegenerative MedicineAnimalsChondrocytesHumansCartilage regenerationChondrocytesInduced pluripotent stem cellsMesenchymal stem cellsOsteoarthritisPersonalized regenerative medicine

Identifiers

PMID38926793
PMCPMC11210138

What OpenQuestion holds

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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.