» Articles » PMID: 37371129

Inverse Regulation of Cartilage Neogenesis at Physiologically Relevant Calcium Conditions by Human Articular Chondrocytes and Mesenchymal Stromal Cells

Overview
Journal Cells
Publisher MDPI
Date 2023 Jun 28
PMID 37371129
Authors
Affiliations
Soon will be listed here.
Abstract

Elaborate bioreactor cultivation or expensive growth factor supplementation can enhance extracellular matrix production in engineered neocartilage to provide sufficient mechanical resistance. We here investigated whether raising extracellular calcium levels in chondrogenic cultures to physiologically relevant levels would provide a simple and inexpensive alternative to enhance cartilage neogenesis from human articular chondrocytes (AC) or bone marrow-derived mesenchymal stromal cells (BMSC). Interestingly, AC and BMSC-derived chondrocytes showed an opposite response to a calcium increase from 1.8 mM to 8 mM by which glycosaminoglycan (GAG) and collagen type II production were elevated during BMSC chondrogenesis but depressed in AC, leading to two-fold higher GAG/DNA values in BMSC-based neocartilage compared to the AC group. According to control treatments with Mg or sucrose, these effects were specific for CaCl rather than divalent cations or osmolarity. Importantly, undesired pro-hypertrophic traits were not stimulated by calcium treatment. Specific induction of PTHrP mRNA and protein by 8.0mM calcium only in AC, along with negative effects of recombinant PTHrP on cartilage matrix production, suggested that the PTHrP pathway contributed to the detrimental effects in AC-based neocartilage. Altogether, raising extracellular calcium levels was discovered as a novel, simple and inexpensive stimulator for BMSC-based cartilage neogenesis without the need for special bioreactors, whereas such conditions should be avoided for AC.

References
1.
Middendorf J, Griffin D, Shortkroff S, Dugopolski C, Kennedy S, Siemiatkoski J . Mechanical properties and structure-function relationships of human chondrocyte-seeded cartilage constructs after in vitro culture. J Orthop Res. 2017; 35(10):2298-2306. DOI: 10.1002/jor.23535. View

2.
Mow V, Kuei S, Lai W, Armstrong C . Biphasic creep and stress relaxation of articular cartilage in compression? Theory and experiments. J Biomech Eng. 1980; 102(1):73-84. DOI: 10.1115/1.3138202. View

3.
Dexheimer V, Gabler J, Bomans K, Sims T, Omlor G, Richter W . Differential expression of TGF-β superfamily members and role of Smad1/5/9-signalling in chondral versus endochondral chondrocyte differentiation. Sci Rep. 2016; 6:36655. PMC: 5111074. DOI: 10.1038/srep36655. View

4.
Winter A, Breit S, Parsch D, Benz K, Steck E, Hauner H . Cartilage-like gene expression in differentiated human stem cell spheroids: a comparison of bone marrow-derived and adipose tissue-derived stromal cells. Arthritis Rheum. 2003; 48(2):418-29. DOI: 10.1002/art.10767. View

5.
Plumb M, Aspden R . The response of elderly human articular cartilage to mechanical stimuli in vitro. Osteoarthritis Cartilage. 2005; 13(12):1084-91. DOI: 10.1016/j.joca.2005.07.002. View