Lumican Regulates Collagen Fibril Assembly: Skin Fragility and Corneal Opacity in the Absence of Lumican

Shukti Chakravarti(University Hospitals of Cleveland), Terry Magnuson(University Hospitals of Cleveland), Jonathan H. Lass(University Hospitals of Cleveland), Karl J. Jepsen(University Hospitals of Cleveland), Christian LaMantia(University Hospitals of Cleveland), Heidi Carroll(University Hospitals of Cleveland)
The Journal of Cell Biology
June 1, 1998
Cited by 739Open Access
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Abstract

Lumican, a prototypic leucine-rich proteoglycan with keratan sulfate side chains, is a major component of the cornea, dermal, and muscle connective tissues. Mice homozygous for a null mutation in lumican display skin laxity and fragility resembling certain types of Ehlers-Danlos syndrome. In addition, the mutant mice develop bilateral corneal opacification. The underlying connective tissue defect in the homozygous mutants is deregulated growth of collagen fibrils with a significant proportion of abnormally thick collagen fibrils in the skin and cornea as indicated by transmission electron microscopy. A highly organized and regularly spaced collagen fibril matrix typical of the normal cornea is also missing in these mutant mice. This study establishes a crucial role for lumican in the regulation of collagen assembly into fibrils in various connective tissues. Most importantly, these results provide a definitive link between a necessity for lumican in the development of a highly organized collagenous matrix and corneal transparency.


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