Evidence map›Paper›PMID 33920285›Full record

ReviewBioengineering (Basel, Switzerland)2021

Rejuvenated Stem/Progenitor Cells for Cartilage Repair Using the Pluripotent Stem Cell Technology.

Naoki Nakayama, Sudheer Ravuri, Johnny Huard

Open access · goldAbstract readReview
In one paragraph

Review in Bioengineering (Basel, Switzerland), 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
0.7field-weighted citation impact, top 30% 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, 5 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Short histological kaleidoscope - recent findings in histology. Part V. About tendons, ligaments, and cartilages.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

3 authors at 1 institution in 1 country.

Naoki NakayamaSteadman Philippon Research Institute, Fort Collins, CO 80526, USA.
Sudheer RavuriSteadman Philippon Research Institute, Vail, CO 81657, USA.
Johnny HuardSteadman Philippon Research Institute, Vail, CO 81657, USA.
Steadman Philippon Research Institute · US

Funding

Bone Abnormalities & Healing Defect in Muscular DystrophyR01AR065445 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUARD, JOHNNY · 2014 to 2018
$1.7M
Articular Cartilage Tissue Engineering with Human Pluripotent Stem CellsR01AR077045 · NIAMS · STEADMAN PHILIPPON RESEARCH INSTITUTE · PI NAKAYAMA, NAOKI · 2021 to 2025
$1.7M
The Use of Senolytic and Anti-Fibrotic Agents to Improve the Beneficial Effect of Bone Marrow Stem Cells for OsteoarthritisUG3AR077748 · NIAMS · STEADMAN PHILIPPON RESEARCH INSTITUTE · PI HUARD, JOHNNY, PHILIPPON, MARC · 2020 to 2020
$522k
Muscle Stem Cells Reprogrammed Through Genome Engineering for Autonomously Regulated Anti-Fibrotic TherapyR21AR072870 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI GUILAK, FARSHID, HUARD, JOHNNY · 2018 to 2019
$416k
Effects of Circulating Factors and Progenitors on Wound Healing during PregnancyR21AR073509 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUARD, JOHNNY · 2018 to 2019
$375k
Ablation of Non-Myogenic Progenitor Cells as a New Therapeutic Approach to Duchenne Muscular DystrophyR21AR074132 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUARD, JOHNNY, KOLONIN, MIKHAIL G · 2019 to 2020
$343k
Development of biological approaches to enhance skeletal muscle rehabilitation after anterior cruciate ligament injuryR21AR075997 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI HUARD, JOHNNY, NARKAR, VIHANG A · 2019 to 2020
$332k
Annie and Bob Graham Distinguished Chair in Stem Cell Biology N/ANIAMS NIH HHS 1R01AR065445-01NIAMS NIH HHS 1R01AR077045-01NIAMS NIH HHS 1R21AR072870-01NIAMS NIH HHS 1R21AR073509-01NIAMS NIH HHS 1R21AR074132-01NIAMS NIH HHS 1R21AR075997-01NIAMS NIH HHS 1UG3AR077748-01NIAMS NIH HHS R01 AR077045
6 · The paper itself

Abstract

It is widely accepted that chondral defects in articular cartilage of adult joints are never repaired spontaneously, which is considered to be one of the major causes of age-related degenerative joint disorders, such as osteoarthritis. Since mobilization of subchondral bone (marrow) cells and addition of chondrocytes or mesenchymal stromal cells into full-thickness defects show some degrees of repair, the lack of self-repair activity in adult articular cartilage can be attributed to lack of reparative cells in adult joints. In contrast, during a fetal or embryonic stage, joint articular cartilage has a scar-less repair activity, suggesting that embryonic joints may contain cells responsible for such activity, which can be chondrocytes, chondroprogenitors, or other cell types such as skeletal stem cells. In this respect, the tendency of pluripotent stem cells (PSCs) to give rise to cells of embryonic characteristics will provide opportunity, especially for humans, to obtain cells carrying similar cartilage self-repair activity. Making use of PSC-derived cells for cartilage repair is still in a basic or preclinical research phase. This review will provide brief overviews on how human PSCs have been used for cartilage repair studies.

Indexed as

cartilagepluripotent stem cellregeneration

Identifiers

PMID33920285
PMCPMC8070387
OpenAlexW3154688801

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.