Evidence map›Paper›PMID 39556314›Full record

ArticleTissue engineering. Part A2025

Decellularized Extracellular Matrix Improves Mesenchymal Stromal Cell Spheroid Response to Chondrogenic Stimuli.

David H Ramos-Rodriguez, Shierly W Fok, Connor J Dorais, Andrea C Filler, Mason Caserta, J Kent Leach

Abstract read
In one paragraph

Article in Tissue engineering. Part A, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Edible Sulfonated Soy Protein Microcarriers for Cultivated Meat Cell Expansion.Journal of biomedical materials research. Part A · 2026
    Article
  2. 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

6 authors.

David H Ramos-RodriguezDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.
Shierly W FokDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.
Connor J DoraisDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.
Andrea C FillerDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.
Mason CasertaDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.
J Kent LeachDepartment of Orthopaedic Surgery, UC Davis Health, Sacramento, California, USA.ORCID 0000-0002-1673-3335

Funding

Identifying the superior ossification pathway for tissue engineered approaches to long bone repairR01AR079211 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI LEACH, J. KENT · 2021 to 2025
$1.9M
MUSCLE: MUsculoSkeletal Clinical Learning Experience Transdisciplinary Musculoskeletal Research Training ProgramT32AR079099 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI J. Kent Leach, Robert L. Randall · 2022 to 2026
$844k
NIAMS NIH HHS R01 AR079211NIAMS NIH HHS T32 AR079099
6 · The paper itself

Abstract

Cartilage regeneration is hindered due to the low proliferative capacity of chondrocytes and the avascular nature of cartilaginous tissue. Mesenchymal stromal cells (MSCs) are widely studied for cartilage tissue engineering, and the aggregation of MSCs into high-density cell spheroids facilitates chondrogenic differentiation due to increased cell-cell contact. Despite the promise of MSCs, the field would benefit from improved strategies to regulate the chondrogenic potential of MSCs differentiated from induced pluripotent stem cells (iPSCs), which are advantageous for their capacity to yield large numbers of required cells. We previously demonstrated the ability of MSC-secreted extracellular matrix (ECM) to promote MSC chondrogenic differentiation, but the combinatorial effect of iPSC-derived MSC (iMSC) spheroids, iMSC-derived decellularized ECM (idECM), and other stimuli (e.g., oxygen tension and transforming growth factor [TGF]-β) on chondrogenic potential has not been described. Similar to MSCs, iMSCs secreted a collagen-rich ECM. When incorporated into spheroids, idECM increased spheroid diameter and promoted chondrogenic differentiation. The combination of idECM loading, chondrogenic media, and hypoxia enhanced glycosaminoglycan (GAG) content 1.6-fold (40.9 ± 4.6 ng vs. 25.6 ± 3.3 ng,

Indexed as

ChondrogenesisDecellularized Extracellular MatrixExtracellular MatrixMesenchymal Stem CellsSpheroids, CellularCell DifferentiationGlycosaminoglycansHumansInduced Pluripotent Stem CellsDecellularized Extracellular MatrixGlycosaminoglycanschondrogenesisdecellularized ECMoxygenspheroidsTGF-β1

Identifiers

PMID39556314
PMCPMC11971541

What Socratic 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 Socratic graph.