Murine tendon function is adversely affected by aggrecan accumulation due to the knockout of ADAMTS5.

J Orthop Res

Departments of Orthopedic Surgery, Rheumatology/Internal Medicine, and Biochemistry, Rush University Medical Center, 1611 W. Harrison Street, Suite 201, Chicago, Illinois 60612, USA.

Published: April 2012

The present study examined the effect of ADAMTS5 (TS5) knockout on the properties of murine flexor digitorum longus (FDL) and Achilles tendons. FDL and Achilles tendons were analyzed using biomechanical testing, histology, and immunohistochemistry; further characterization of FDL tendons was conducted using transmission electron microscopy (collagen fibril ultrastructure), SDS-PAGE (collagen content and type), fluorescence-assisted carbohydrate electrophoresis for chondroitin sulfate and hyaluronan, and Western blotting for aggrecan, versican, and decorin abundance and distribution. FDL tendons of TS5(-/-) mice showed a 33% larger cross-sectional area, increased collagen fibril area fraction, and decreased material properties relative to those of wild type mice. In TS5(-/-) mice, aggrecan accumulated in the pericellular matrix of tendon fibroblasts. In Achilles tendons, cross-sectional area, stress relaxation, and structural properties were similar in TS5(-/-) and wild type mice; however, the TS5(-/-) tendons exhibited a higher tensile modulus and a weakened enthesis. These results demonstrate that TS5 deficiency disturbs normal tendon collagen organization and alters biomechanical properties. Hence, the role of ADAMTS5 in tendon is to remove pericellular and interfibrillar aggrecan to maintain the molecular architecture responsible for normal tissue function.

Download full-text PDF

Source
http://dx.doi.org/10.1002/jor.21558DOI Listing

Publication Analysis

Top Keywords

achilles tendons
12
fdl achilles
8
fdl tendons
8
collagen fibril
8
ts5-/- mice
8
cross-sectional area
8
wild type
8
type mice
8
mice ts5-/-
8
tendons
6

Similar Publications

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!