Type VIII collagen has a restricted distribution in specialized extracellular matrices.
Open Access
- 1 August 1988
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 107 (2) , 721-730
- https://doi.org/10.1083/jcb.107.2.721
Abstract
A pepsin-resistant triple helical domain (chain 50,000 Mr) of type VIII collagen was isolated from bovine corneal Descemet''s membrane and used as an immunogen for the production of mAbs. An antibody was selected for biochemical and tissue immunofluorescence studies which reacted both with Descemet''s membrane and with type VIII collagen 50,000-Mr polypeptides by competition ELISA and immunoblotting. This antibody exhibited no cross-reactivity with collagen types I-VI by competition ELISA. The mAb specifically precipitated a high molecular mass component of type VIII collagen (EC2, of chain 125,000 Mr) from the culture medium of subconfluent bovine corneal endothelial cells metabolically labeled for 24 h. In contrast, confluent cells in the presence of FCS and isotope for 7 d secreted a collagenous component of chain 60,000 Mr that did not react with the anti-type VIII collagen IgG. Type VIII collagen therefore appears to be synthesized as a discontinuous triple helical molecule with a predomnant chain 125,000 Mr by subconfluent, proliferating cells in culture. Immunofluorescence studies with the mAb showed that type VIII collagen was deposited as fibrils in the extracellular matrix of corneal endothelial cells. In the fetal calf, type VIII collagen was absent from basement membranes and was found in a limited number of tissues. In addition to the linear staining pattern observed in the Descemet''s membrane, type VIII collagen was found in highly fibrillar arrays in the ocular sclera, in the meninges surrounding brain, spinal cord, and optic nerve, and in periosteum and perichondrium. Fine fibrils were evident in the white matter of spinal cord, whereas a more generalized staining was apparent in the matrices of cartilage and bone. Despite attempts to unmask the epitope, type VIII collagen was not found in aorta, kidney, lung, liver, skin, and ligament. We conclude that this unusual collagen is a component of certain specialized extracellular matrices, several of which are derived from the neural crest.Keywords
This publication has 31 references indexed in Scilit:
- Transient expression of collagen type II at epitheliomesenchymal interfaces during morphogenesis of the cartilaginous neurocraniumDevelopmental Biology, 1986
- Isolation and characterization of type VIII collagen synthesized by cultured rabbit corneal endothelial cells. A conventional structure replaces the interrupted-helix model.Journal of Biological Chemistry, 1986
- Characterization of the Descemet's membrane/posterior collagenous layer isolated from Fuchs' endothelial dystrophy corneasExperimental Eye Research, 1984
- Classification of Corneal Endothelial Disorders Based on Neural Crest OriginOphthalmology, 1984
- Matrices control the differentiation of cartilage and bone.1984
- THE BASEMENT-MEMBRANE OF BOVINE CORNEAL ENDOTHELIAL-CELLS IN CULTURE WITH BETA-AMINOPROPIONITRILE - BIOSYNTHESIS OF HEXAGONAL LATTICES COMPOSED OF A 160 NM DUMBBELL-SHAPED STRUCTURE1984
- TYPE-VIII COLLAGEN - SYNTHESIS BY NORMAL AND MALIGNANT-CELLS IN CULTURE1984
- The presence of EC collagen and type IV collagen in bovine Descemet's membranesBiochemical and Biophysical Research Communications, 1983
- Monoclonal antibody analysis of ocular basement membranes during developmentDevelopmental Biology, 1983
- Monoclonal antibodies against chicken type V collagen: production, specificity, and use for immunocytochemical localization in embryonic cornea and other organsThe Journal of cell biology, 1983