Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers

Cartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondroc...

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Main Authors: Krishi Patel, Derya Ozhava, Yong Mao
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Gels
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Online Access:https://www.mdpi.com/2310-2861/11/3/199
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author Krishi Patel
Derya Ozhava
Yong Mao
author_facet Krishi Patel
Derya Ozhava
Yong Mao
author_sort Krishi Patel
collection DOAJ
description Cartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondrocytes are isolated, cultured in vitro to expand the cell population, and then implanted into the damaged site. However, in vitro expansion of chondrocytes on standard 2D culture surfaces leads to dedifferentiation (loss of the chondrocyte phenotype), and the delivery of detached cells has proven to be ineffective. To overcome these limitations, the matrix-assisted ACI (MACI) procedure was developed. In MACI, matrices such as hydrogels and microspheres are used as cell carriers or scaffolds to deliver expanded chondrocytes, enhancing cell viability and precision delivery. To streamline the two key steps of MACI—cell expansion and delivery—this study aims to investigate various configurations of gelatin-based hydrogels for their potential to support both cell expansion and delivery as a single step. This study evaluated gelatin microspheres (Gel MS), micronized photo-crosslinked GelMA microparticles (GelMA MP), and bulky GelMA hydrogels containing cells (GelMA HG). Cell growth, maintenance of the chondrocyte phenotype, and cartilage extracellular matrix (ECM) production were assessed in pellet cultures for cells grown on/in these carriers, compared with cells cultured on tissue culture-treated polystyrene (TCP). Our results demonstrate that normal human knee articular chondrocytes exhibit robust growth on Gel MS and form aggregates enriched with glycosaminoglycan-rich ECM. Gel MS outperformed both GelMA MP and GelMA HG as a cell carrier by both supporting long-term cell growth with reduced dedifferentiation and precision delivery.
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spelling doaj-art-101a3ff5533643f4bb2506c9f408056e2025-08-20T02:42:30ZengMDPI AGGels2310-28612025-03-0111319910.3390/gels11030199Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell CarriersKrishi Patel0Derya Ozhava1Yong Mao2Laboratory for Biomaterials Research, Department of Chemistry and Chemical Biology, Rutgers University, 145 Bevier Rd., Piscataway, NJ 08854, USALaboratory for Biomaterials Research, Department of Chemistry and Chemical Biology, Rutgers University, 145 Bevier Rd., Piscataway, NJ 08854, USALaboratory for Biomaterials Research, Department of Chemistry and Chemical Biology, Rutgers University, 145 Bevier Rd., Piscataway, NJ 08854, USACartilage damage is common in sports injuries and cartilage-related diseases, such as degenerative joint and rheumatic disorders. Autologous chondrocyte implantation (ACI) is a widely used cell-based therapy for repairing cartilage damage in clinical practice. In this procedure, a patient’s chondrocytes are isolated, cultured in vitro to expand the cell population, and then implanted into the damaged site. However, in vitro expansion of chondrocytes on standard 2D culture surfaces leads to dedifferentiation (loss of the chondrocyte phenotype), and the delivery of detached cells has proven to be ineffective. To overcome these limitations, the matrix-assisted ACI (MACI) procedure was developed. In MACI, matrices such as hydrogels and microspheres are used as cell carriers or scaffolds to deliver expanded chondrocytes, enhancing cell viability and precision delivery. To streamline the two key steps of MACI—cell expansion and delivery—this study aims to investigate various configurations of gelatin-based hydrogels for their potential to support both cell expansion and delivery as a single step. This study evaluated gelatin microspheres (Gel MS), micronized photo-crosslinked GelMA microparticles (GelMA MP), and bulky GelMA hydrogels containing cells (GelMA HG). Cell growth, maintenance of the chondrocyte phenotype, and cartilage extracellular matrix (ECM) production were assessed in pellet cultures for cells grown on/in these carriers, compared with cells cultured on tissue culture-treated polystyrene (TCP). Our results demonstrate that normal human knee articular chondrocytes exhibit robust growth on Gel MS and form aggregates enriched with glycosaminoglycan-rich ECM. Gel MS outperformed both GelMA MP and GelMA HG as a cell carrier by both supporting long-term cell growth with reduced dedifferentiation and precision delivery.https://www.mdpi.com/2310-2861/11/3/199chondrocytesgelatin microspheresGelMAmicroparticlesMACIdedifferentiation
spellingShingle Krishi Patel
Derya Ozhava
Yong Mao
Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
Gels
chondrocytes
gelatin microspheres
GelMA
microparticles
MACI
dedifferentiation
title Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
title_full Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
title_fullStr Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
title_full_unstemmed Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
title_short Expansion and Delivery of Human Chondrocytes on Gelatin-Based Cell Carriers
title_sort expansion and delivery of human chondrocytes on gelatin based cell carriers
topic chondrocytes
gelatin microspheres
GelMA
microparticles
MACI
dedifferentiation
url https://www.mdpi.com/2310-2861/11/3/199
work_keys_str_mv AT krishipatel expansionanddeliveryofhumanchondrocytesongelatinbasedcellcarriers
AT deryaozhava expansionanddeliveryofhumanchondrocytesongelatinbasedcellcarriers
AT yongmao expansionanddeliveryofhumanchondrocytesongelatinbasedcellcarriers