The DOI matches its Crossref record.
Type III collagen can be present on banded collagen fibrils regardless of fibril diameter.
Open accessAbstract
Monoclonal antibodies that recognize an epitope within the triple helix of type III collagen have been used to examine the distribution of that collagen type in human skin, cornea, amnion, aorta, and tendon. Ultrastructural examination of those tissues indicates antibody binding to collagen fibrils in skin, amnion, aorta, and tendon regardless of the diameter of the fibril. The antibody distribution is unchanged with donor age, site of biopsy, or region of tissue examined. In contrast, antibody applied to adult human cornea localizes to isolated fibrils, which appear randomly throughout the matrix. These studies indicate that type III collagen remains associated with collagen fibrils after removal of the amino and carboxyl propeptides, and suggests that fibrils of skin, tendon, and amnion (and presumably many other tissues that contain both types I and III collagens) are copolymers of at least types I and III collagens.
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Cited by
Liu, X., Wu, H., Byrne, M., Krane, S., & Jaenisch, R. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.5.1852 · Cited by 614
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Birk, D. E., Fitch, J. M., Babiarz, J. P., Doane, K. J., & Linsenmayer, T. F. (1990) · Journal of Cell Science · doi:10.1242/jcs.95.4.649 · Cited by 596
Le Guellec, D., Morvan-Dubois, G., & Sire, J.-Y. (2004) · The International Journal of Developmental Biology · doi:10.1387/ijdb.15272388 · Cited by 286
The hepatic extracellular matrix: I. Components and distribution in normal liver
Martinez-Hernandez, A., & Amenta, P. S. (1993) · Virchows Archiv A Pathological Anatomy and Histopathology · doi:10.1007/bf01606425 · Cited by 200
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Malfait, F. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.04.013 · Cited by 113
Smith, L. T., Schwarze, U., Goldstein, J., & Byers, P. H. (1997) · Journal of Investigative Dermatology · doi:10.1111/1523-1747.ep12286441 · Cited by 99
D'hondt, S., Guillemyn, B., Syx, D., Symoens, S., De Rycke, R., Vanhoutte, L., Toussaint, W., Lambrecht, B. N., De Paepe, A., Keene, D. R., et al. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.03.008 · Cited by 79
Self-citationParkin, J. D., San Antonio, J. D., Persikov, A. V., Dagher, H., Dalgleish, R., Jensen, S. T., Jeunemaitre, X., & Savige, J. (2017) · PLOS ONE · doi:10.1371/journal.pone.0175582 · Cited by 39
Metadata
- Authors
- Keene, D. R., Sakai, L. Y., Bächinger, H. P., & Burgeson, R. E.
- Venue
- The Journal of cell biology
- Publisher
- Rockefeller University Press
- Published
- 1987-11-01
- Volume
- 105
- Issue
- 5
- Pages
- 2393-2402
- ISSN
- 0021-9525 (ISSN-L)
- 1540-8140
- OpenAlex
- W2069881257
- Cited by
- 272
- References
- 0
- FWCI
- 17.16
- Type
- journal article
- Language
- en
- Open access
- green
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
