| Literature DB >> 31550133 |
Biao Han1, Qing Li1, Chao Wang1, Pavan Patel1, Sheila M Adams2, Basak Doyran1, Hadi T Nia3, Ramin Oftadeh4, Siyuan Zhou5, Christopher Y Li6, X Sherry Liu7, X Lucas Lu8, Motomi Enomoto-Iwamoto9, Ling Qin7, Robert L Mauck7, Renato V Iozzo10, David E Birk2, Lin Han1.
Abstract
Joint biomechanical functions rely on the integrity of cartilage extracellular matrix. Understanding the molecular activities that govern cartilage matrix assembly is critical for developing effective cartilage regeneration strategies. This study elucidated the role of decorin, a small leucine-rich proteoglycan, in the structure and biomechanical functions of cartilage. In decorin-null cartilage, we discovered a substantial reduction of aggrecan content, the major proteoglycan of cartilage matrix, and mild changes in collagen fibril nanostructure. This loss of aggrecan resulted in significantly impaired biomechanical properties of cartilage, including decreased modulus, elevated hydraulic permeability, and reduced energy dissipation capabilities. At the cellular level, we found that decorin functions to increase the retention of aggrecan in the neo-matrix of chondrocytes, rather than to directly influence the biosynthesis of aggrecan. At the molecular level, we demonstrated that decorin significantly increases the adhesion between aggrecan and aggrecan molecules and between aggrecan molecules and collagen II fibrils. We hypothesize that decorin plays a crucial structural role in mediating the matrix integrity and biomechanical functions of cartilage by providing physical linkages to increase the adhesion and assembly of aggrecan molecules at the nanoscale.Entities:
Keywords: articular cartilage; decorin; extracellular matrix; molecular assembly; nanomechanics; poroelasticity; proteoglycan
Year: 2019 PMID: 31550133 PMCID: PMC6892632 DOI: 10.1021/acsnano.9b04477
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881