Age-dependent mechanical properties of tail tendons in wild-type and mimecan gene-knockout mice - A preliminary study.

Mimecan, or osteoglycin, belongs to the family of small leucine-rich proteoglycans. In connective tissues mimecan is implicated in the development and maintenance of normal collagen fibrillar organization. Since collagen fibrils are responsible for tissue reinforcement, the absence of mimecan could lead to abnormal tissue mechanical properties. Here, we carried out a preliminary investigation of possible changes in the mechanical properties of tendons in mice lacking a functional mimecan gene, as a function of age. Tail tendons were dissected from mimecan gene knockout (KO) and wild type (WT) mice at ages 1, 4 and 8 months and mechanical properties evaluated using a microtensile testing equipment. Mimecan gene knockout resulted in changes in tendon elasticity- and fracture-related properties. While tendons of WT mice exhibited enhanced mechanical properties with increasing age, this trend was notably attenuated in mimecan KO tendons, with the exception of fracture strain. When genotype and age were considered as cross factors, the diminution in the mechanical properties of mimecan KO tendons was significant for yield strength, modulus and fracture strength. This effect appeared to affect the mice at 4 month old. These preliminary results suggest that mimecan may have a role in regulating age-dependent mechanical function in mouse tail tendon.

A structural investigation of corneal graft failure in suspected recurrent keratoconus.

PURPOSE: Penetrating keratoplasty was performed on the right eye of a 51-year-old patient diagnosed with advanced bilateral keratoconus. Thirteen years later, an 8.5 mm regraft was required as a result of gross vascularisation, a poor epithelium, and suspected recurrent keratoconus. To learn more about the structural basis for graft failure, we examined the removed tissue for the presence of abnormalities in the stroma and limiting membranes. METHODS: X-ray scattering and electron microscopy were used to study the failed-graft tissue to provide information on the integrity of the limiting membranes and the diameter, dominant orientation, and distribution of collagen within the corneal stroma. The findings were compared with similar structural data from normal and keratoconus corneas. RESULTS: In contrast to the keratoconus cornea, a normal orientation and distribution of collagen was seen throughout most of the failed-graft tissue, although abnormalities were observed in the infero-nasal quadrant at the original graft/host junction. The average diameter of collagen fibrils in the failed-graft button did not differ from that of normal corneas. CONCLUSIONS: The structural abnormalities identified in this case of graft failure were not consistent with those typically seen in keratoconus. The clear demarcation of the graft/host boundary 13 years after surgery suggests that a normal stromal collagen arrangement may never be fully achieved in corneal graft wounds.