Type XIV Collagen Regulates Fibrillogenesis: PREMATURE COLLAGEN FIBRIL GROWTH AND TISSUE DYSFUNCTION IN NULL MICE

J Biol Chem. 2009 Mar 27;284(13):8427-38. doi: 10.1074/jbc.M805582200. Epub 2009 Jan 9.

Abstract

Type XIV collagen is a fibril-associated collagen with an interrupted triple helix. This collagen interacts with the fibril surface and has been implicated as a regulator of fibrillogenesis; however, a specific role has not been elucidated. Functional roles for type XIV collagen were defined utilizing a new type XIV collagen-deficient mouse line. This line was produced using a conventional targeted knock-out approach. Col14a1(-/-) mice were devoid of type XIV collagen, whereas heterozygous mice had reduced synthesis. Both mutant Col14a1 genotypes were viable with a grossly normal phenotype; however, mature skin exhibited altered mechanical properties. Prior to evaluating tendon fibrillogenesis in type XIV collagen-deficient mice, the developmental expression patterns were analyzed in wild-type flexor digitorum longus (FDL) tendons. Analyses of mRNA and protein expression indicated tissue-specific temporal expression that was associated with the early stages in fibrillogenesis. Ultrastructural analyses of wild-type and null tendons demonstrated premature fibril growth and larger fibril diameters in tendons from null mice at postnatal day 4 (P4). However, fibril structure in mature tendons was normal. Biomechanical studies established a direct structure/function relationship with reduced strength in P7-null tendons. However, the biomechanical properties in P60 tendons were comparable in null and wild-type mice. Our results indicate a regulatory function for type XIV collagen in early stages of collagen fibrillogenesis with tissue differences.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Collagen / genetics*
  • Extracellular Matrix / metabolism*
  • Extracellular Matrix / ultrastructure
  • Glycoproteins / genetics*
  • Mice
  • Mice, Knockout
  • Organ Specificity
  • Protein Structure, Secondary / genetics
  • Skin / metabolism*
  • Skin / ultrastructure
  • Tendons / metabolism*
  • Tendons / ultrastructure

Substances

  • Col14a1 protein, mouse
  • Glycoproteins
  • Collagen