Evidence map›Paper›PMID 42911321›Full record

ArticleTissue engineering and regenerative medicine2026

Ion-Enriched Solution Improves the Adhesion of Freshly Thawed Umbilical Cord-Derived Mesenchymal Stem Cells and Supports Cartilage Repair in a Rat Full-Thickness Cartilage Defect Model.

Daeun Lee, Min Ji Lee, Jian Jiang, Taewoo Kim, Chris Hyunchul Jo

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Article in Tissue engineering and regenerative medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Daeun LeeDepartment of Translational Medicine, Seoul National University College of Medicine, Seoul, Korea.
Min Ji LeeDepartment of Translational Medicine, Seoul National University College of Medicine, Seoul, Korea.
Jian JiangDepartment of Translational Medicine, Seoul National University College of Medicine, Seoul, Korea.
Taewoo KimDepartment of Orthopedic Surgery, SMG-SNU Boramae Medical Center, Seoul National University College of Medicine, 20 Boramae-ro 5-gil, Dongjak-gu, Seoul, 07061, Korea.
Chris Hyunchul JoDepartment of Translational Medicine, Seoul National University College of Medicine, Seoul, Korea. chrisjo@snu.ac.kr.ORCID http://orcid.org/0000-0002-6161-5442

Funding

Korea Health Industry Development Institute HI20C0386Ministry of Health and Welfare 22C0608L1Ministry of Science and ICT, South Korea 22C0608L1Ministry of SMEs and Startups S3283968Seoul Metropolitan Government Seoul National University Boramae Medical Center 04-2024-0010Seoul Metropolitan Government Seoul National University Boramae Medical Center 04-2025-0000
6 · The paper itself

Abstract

backgroundFreshly thawed umbilical cord-derived mesenchymal stem cells (FT-UC MSCs) often show reduced post-thaw functionality, limiting their use as off-the-shelf cell therapies. This study investigated whether an ion-enriched solution (IES) could improve FT-UC MSC adhesion and cartilage repair-associated outcomes.

methodsUC MSCs were categorized as cryopreserved and culture-recovered UC MSCs (CP-UC MSCs) or FT-UC MSCs. Adhesion was assessed in vitro on type I collagen and ex vivo on human osteoarthritic cartilage using saline, IES, or magnesium chloride as carriers. In vivo, rats with full-thickness cartilage defects received intra-articular injections of IES alone, CP-UC MSCs in saline, or FT-UC MSCs in IES. Cartilage repair was evaluated by ICRS macroscopic and histological scoring, immunohistochemistry, and static weight-bearing.

resultsFT-UC MSCs showed reduced proliferation, metabolic activity, and adhesion compared with CP-UC MSCs. IES significantly enhanced FT-UC MSC adhesion in vitro and ex vivo, with magnesium chloride (MgCl

conclusionFT-UC MSCs delivered with IES showed improved post-thaw adhesive function and repair-associated outcomes comparable to CP-UC MSCs delivered with saline in a rat full-thickness cartilage defect model. These findings support the potential utility of IES as a practical delivery carrier for freshly thawed UC-MSCs without an extended culture-recovery step, while further studies including an FT-UC MSCs + saline group are required to isolate the specific in vivo contribution of IES.

Indexed as

AdhesionCartilage repairCryopreservationMesenchymal stem cells (MSC)Osteoarthritis

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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.