Alper DUNKI
Articular Cartilage: Structure, Components, and Clinical Relevance
Overview
Spot Knowledge – Articular Cartilage
Composition: 95% ECM (water, collagen, proteoglycans), 5% chondrocytes
Water: 65–80%, enables load-bearing, nutrient transport
Collagen: >50% dry weight, mainly type II (90–95%); tensile strength
Proteoglycans: 10–15% dry weight; aggrecan + GAGs provide compressive resilience
Zones:
Superficial (parallel collagen, friction reduction)
Transitional (irregular, load distribution)
Deep (vertical, compressive strength)
Calcified (anchors to bone)Functions: Low-friction motion, load distribution, joint stability, resistance to forces
Clinical relevance:
Limited healing (avascular)
Water/collagen/PG imbalance → osteoarthritis
Collagen II & X defects → chondrodysplasias
PG loss → elasticity ↓, cartilage breakdown
Articular Cartilage: Structure, Components, and Clinical Relevance
Overview
Articular cartilage is composed predominantly of extracellular matrix (ECM, ~95%) and a small number of chondrocytes (~5%). Chondrocytes maintain ECM homeostasis throughout life. The main components of ECM are water, collagen, and proteoglycans.
Water
Water accounts for 65–80% of cartilage. It is 80% in the superficial zone and 65% in the deep zone.
Water plays a critical role in load-bearing by deforming in response to compression.
Its movement through ECM pores, along with frictional resistance and pressurization, provides high load-bearing capacity.
Facilitates the transport of nutrients and metabolites.
Alterations in water content affect permeability, stiffness, and elastic modulus.
Collagen
Collagen constitutes more than 50% of the dry weight and 10–20% of the wet weight.
Provides tensile and shear strength.
Type II collagen accounts for 90–95% of the total.
Minor collagens include types V, VI, IX, X, and XI.
Type VI: increases in early osteoarthritis.
Type X: produced by hypertrophic chondrocytes during endochondral ossification; associated with calcification.
The unique amino acid composition (glycine, proline, hydroxyproline, hydroxylysine) forms a triple-helix structure.
Covalent cross-links between fibrils enhance durability.
Defects in collagen type II and X can lead to achondroplasia, spondyloepiphyseal dysplasia, Kniest dysplasia, and metaphyseal chondrodysplasia.
Proteoglycans
Proteoglycans constitute 10–15% of dry weight and provide compressive strength.
Synthesized by chondrocytes and secreted into the ECM.
Contain glycosaminoglycans (GAGs) composed of repeating disaccharides: chondroitin sulfate and keratan sulfate.
Chondroitin sulfate decreases with age, keratan sulfate increases.
The most important proteoglycan is aggrecan, which consists of a long protein core with GAG side chains.
Aggrecan molecules aggregate with hyaluronic acid and link proteins, imparting resilience to the matrix.
Interact with collagen fibrils to form a robust network.
Zones
Histologically, articular cartilage is organized into four zones:
Superficial zone: Collagen fibers are aligned parallel; reduces friction.
Transitional zone: Fibers are irregular; distributes load.
Deep zone: Fibers are vertically aligned; provides high compressive strength.
Calcified zone: Anchors cartilage to bone.
Functions
Provides low-friction joint motion.
Distributes loads and contributes to joint stability.
Resists compressive and tensile forces.
Maintains nutrient transport and metabolic homeostasis.
Clinical Relevance
Cartilage is avascular, with limited intrinsic healing capacity.
Alterations in water, collagen, and proteoglycan content are associated with degenerative disorders such as osteoarthritis.
Defects in type II and X collagen result in genetic chondrodysplasias.
Loss of proteoglycans leads to reduced elasticity and cartilage breakdown.
Reference
1. Guo L, Li P, Rong X, Wei X. Key roles of the superficial zone in articular cartilage physiology, pathology, and regeneration. Inflamm Regen. 2024;44:21. doi:10.1186/s41232-022-00202-0
2. Alcaide-Ruggiero L, Cugat R, Domínguez JM. Proteoglycans in Articular Cartilage and Their Contribution to Chondral Injury and Repair Mechanisms. Int J Mol Sci. 2023;24(14):11472. doi:10.3390/ijms241411472
3. Karpiński R, Szczodry M, Zawadzki G. Articular Cartilage: Structure, Biomechanics, and the Potential of Regenerative Medicine. Appl Sci. 2025;15(12):6896. doi:10.3390/app15126896
