Understanding factors affecting human chondrocyte culturing: an experimental study.

Cell Tissue Bank

Stem Cell Institute, Ankara University, Cevizlidere Mah., Ceyhun Atuf Kansu Cd. No: 169, 06520, Balgat, Ankara, Turkey.

Published: December 2020

AI Article Synopsis

  • Researchers aimed to improve cartilage injury treatment through optimized chondrocyte culture isolation techniques for regenerative medicine.
  • They found that using collagenase type II at a specific concentration maintained key cartilage features, but noted that passaging decreased critical cartilage expressions (COL2 and GAG).
  • The study also identified Advanced DMEM as an effective medium to maintain chondrocyte characteristics, leading to the approval for using their developed manufacturing process in clinical applications.

Article Abstract

Over the years, surgical strategies have been developed in hope of full regeneration of the injured cartilage. In our study, we aimed to develop an optimized chondrocyte culture isolation technique as an active ingredient of a standardized autologous chondrocte implantation product, which is able to maintain the phenotype along with the molecular features of the cartilage. We compared different enzymes, which suggested optimal performance with collagenase type II at 5 mg/ml concentration. Thereafter, we observed that COL2 and GAG expression is substantially reduced with passaging. There was a need to omit passaging to reach the optimal isolation method. We then tested various growth factors and media in order to maintain the natural character of chondrocytes. Our study also suggested the highest COL2 and GAG expressions with the highest recovery in the presence of Advanced DMEM. Autologous chondrocyte implantation manufacturing approval was recently received from the national competent authority, making it possible to utilize the process engineering protocol developed with this study at our Tissue and Cell Manufacturing Center as a part of the autologous chondrocyte implantation manufacturing standard operation procedure (SOP).

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10561-020-09847-yDOI Listing

Publication Analysis

Top Keywords

col2 gag
8
autologous chondrocyte
8
chondrocyte implantation
8
understanding factors
4
factors human
4
chondrocyte
4
human chondrocyte
4
chondrocyte culturing
4
culturing experimental
4
study
4

Similar Publications

Polydeoxynucleotide-Loaded Visible Light Photo-Crosslinked Gelatin Methacrylate Hydrogel: Approach to Accelerating Cartilage Regeneration.

Gels

January 2025

Department of Polymer Nano Science & Technology and Polymer Materials Fusion Research Center, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si 54896, Jeonbuk, Republic of Korea.

Articular cartilage faces challenges in self-repair due to the lack of blood vessels and limited chondrocyte concentration. Polydeoxyribonucleotide (PDRN) shows promise for promoting chondrocyte growth and cartilage regeneration, but its delivery has been limited to injections. Continuous PDRN delivery is crucial for effective cartilage regeneration.

View Article and Find Full Text PDF
Article Synopsis
  • The study investigates the role of TNFα in inflammatory models for osteoarthritis, focusing on how its effects vary with concentration and chondrocyte growth stages.
  • Bovine chondrocytes were used, cultured in a 3D pellet, and exposed to TNFα for 48 hours, revealing that a concentration of 10 ng/mL was required to significantly induce inflammation.
  • Results showed that higher passages of chondrocytes (especially passage 3) were more sensitive to TNFα, affecting both gene expression of catabolic/inflammatory markers and protein levels of certain cytokines.
View Article and Find Full Text PDF

Introduction: Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular differentiation by activating smad-4/5 pathways. KGN has been proposed as a feasible alternative to expensive biologic growth factors, such as transforming growth factor β, which remain under strict regulatory scrutiny when it comes to use in patients.

Method: This study reports the previously unexplored effects of KGN stimulation on cartilage- derived mesenchymal progenitor cells (CPCs), which have been shown to be effective in applications of cell-based musculoskeletal tissue regeneration.

View Article and Find Full Text PDF

differentiation of human induced pluripotent stem cells into temporomandibular joint disc like cells.

Heliyon

January 2024

Key Lab of Stomatology of State Ethnic Affairs Commission, Northwest Minzu University, No.1 Northwest Xin Cun, Chengguan District, Lanzhou, 7300030, China.

Temporomandibular joint discs (TMJ discs) are unable to repair themselves in disease states, while induced stem cell differentiation is a common method to repair tissue defects. Nowadays, kinds of stem cells are attempted for tissue regeneration of TMJ disc, but these methods have several downsides, which limit their wide application. The proliferation and differentiation ability of human induced pluripotent stem cells (hiPSC) provides a new research direction for TMJ disc tissue regeneration.

View Article and Find Full Text PDF
Article Synopsis
  • Chemonucleolysis is effective for creating models of intervertebral disc (IVD) degeneration, but more comparisons of enzyme effects are needed for better understanding of degeneration characteristics.
  • In this study, three enzymes (papain, chondroitinase ABC, and collagenase II) were tested on bovine IVDs, revealing significant differences in degeneration, with papain causing the most damage.
  • Overall, papain and collagenase mimicked advanced degeneration while chondroitinase ABC reflected early-stage degeneration, highlighting the utility of chemonucleolysis in research.
View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!