Long-term evaluation of human iPSC-derived cartilage for repairing chondral defects

Induced pluripotent stem cells (iPSCs) have demonstrated superior capacity to regenerate hyaline cartilage compared to mesenchymal stromal cells (MSCs). However, most previous animal studies have only conducted short-term assessments. We performed a long-term (8 weeks) in vitro chondrogenesis of human iPSC-derived multipotent progenitor cells (iMPCs) and human MSCs. The expression levels of hypertrophy-related genes were significantly lower in the iMPC group compared to the MSC group, such as collagen type X being 5-fold lower on day 56. In the animal study, implants from the iMPC group maintained more matrix than the MSC group at both short and long-term time points (12 and 48 weeks). Importantly, at 48 weeks, the native cartilage surrounding the defect areas in some rats from the MSC group showed severe degradation, which was not observed in the iMPC group. In conclusion, iMPCs represent a safe and effective cell source for long-term hyaline cartilage repair.

Authors

Institutions

Publication Details

Journal
npj Regenerative Medicine
Published
2025-12-24
DOI
https://doi.org/10.1038/s41536-025-00447-6
Primary Topic
Osteoarthritis Treatment and Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Long-term evaluation of human iPSC-derived cartilage for repairing chondral defects

Sophie Hines, Elizabeth R Kats, Jiangyinzi Shang, Yangfan Lu et al.
npj Regenerative Medicine
Osteoarthritis Treatment and Mechanisms
article

Long-term evaluation of human iPSC-derived cartilage for repairing chondral defects

Sophie Hines, Elizabeth R Kats, Jiangyinzi Shang, Yangfan Lu, H S Lin, Jia-Jun Liu, Shotaro Kamijo, Silvia Liu, MaCalus V. Hogan
article en

Abstract

Induced pluripotent stem cells (iPSCs) have demonstrated superior capacity to regenerate hyaline cartilage compared to mesenchymal stromal cells (MSCs). However, most previous animal studies have only conducted short-term assessments. We performed a long-term (8 weeks) in vitro chondrogenesis of human iPSC-derived multipotent progenitor cells (iMPCs) and human MSCs. The expression levels of hypertrophy-related genes were significantly lower in the iMPC group compared to the MSC group, such as collagen type X being 5-fold lower on day 56. In the animal study, implants from the iMPC group maintained more matrix than the MSC group at both short and long-term time points (12 and 48 weeks). Importantly, at 48 weeks, the native cartilage surrounding the defect areas in some rats from the MSC group showed severe degradation, which was not observed in the iMPC group. In conclusion, iMPCs represent a safe and effective cell source for long-term hyaline cartilage repair.

npj Regenerative MedicineVol. 11(1)
SHOWA Medical University (JP), Central South University (CN), University of Pittsburgh (US), UPMC Health System (US), University of Pittsburgh Medical Center (US), Xiangya Hospital Central South University (CN)
University of Pittsburgh, Central South University, Musculoskeletal Research Center, Washington University in St. Louis, Biomedical Research Council
Openalex Percentile: Top 28%
Osteoarthritis Treatment and Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Long-term evaluation of human iPSC-derived cartilage for repairing chondral defects — Sophie Hines, Elizabeth R Kats, et al. · npj Regenerative Medicine (2025) | TGRS Research Map | TGRS