The formation of cross-linkages betweenand within collagen is catalyzed by lysyl oxidase, which can be inhibited by β-aminopropionitrile (BAPN), a lathyrogen from sweet pea (Lathyrus odoratus) seeds. The quality and integrity of the collagenous template of skeletal elements depend on an appropriate concentration of collagen cross-links. In this study, chick embryos treated in ovo with BAPN on embryonic days (ED) 4-9 were found to develop multiple skeletal deformities. The most readily discernible and highly reproducible deformity was evident in the tibiotarsus, on which we focused to explore the chronology of the malformation process. Several lines of observation indicated that the bending deformity observable at ED10 in the tibiotarsus was inducible by BAPN administered on ED4-8; in other words, administration of BAPN on ED8 was sufficient to induce the deformity by ED10, whereas administration on ED9 was ineffective. Ultrastructurally, osteoclasts appeared to show enhanced activity in the medullary surface of the bone collar after BAPN administration. In addition, bone hyperplasia associated with the bending deformity was suggested to be correlated with higher osteoblast activity on the concave (or flexor) side of the tibiotarsal skeleton. These findings indicate that the bending deformity due to reduced mechanical integrity of the collagenous template is also associated with aberrant bone remodeling.
(J Oral Sci 58, 255-263, 2016)Keywords: β-aminopropionitrile; lathyrogen; bone development; skeletal deformity.
IntroductionEmbryonic skeletal elements (cartilage and bone) are fundamentally composed of extracellular collagen fibrils. In the process of ontogenesis, a collagenous template becomes calcified directly or via cartilage to build a specific bony skeleton for each species (1,2), and also, at appropriate sites, cartilaginous tissue itself functions as part of the complete skeletal system. Therefore, the quality and integrity of the collagenous template is particularly crucial for building a skeleton with sufficient inherent strength. The required properties of template collagenous tissue are closely related to the formation of cross-links both between and within collagen molecules (3-5). Such cross-link formation is catalyzed by lysyl oxidase (LOX, EC1.4.3.13), an amine oxidase that converts peptidyl lysine side chains in collagen to allysine, the latter then forming covalent cross-linkages (6,7).