Functional Differences between Keratins of Stratified and Simple Epithelia
Open Access
- 19 October 1998
- journal article
- case report
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 143 (2) , 487-499
- https://doi.org/10.1083/jcb.143.2.487
Abstract
Dividing populations of stratified and simple epithelial tissues express keratins 5 and 14, and keratins 8 and 18, respectively. It has been suggested that these keratins form a mechanical framework important to cellular integrity, since their absence gives rise to a blistering skin disorder in neonatal epidermis, and hemorrhaging within the embryonic liver. An unresolved fundamental issue is whether different keratins perform unique functions in epithelia. We now address this question using transgenic technology to express a K16-14 hybrid epidermal keratin transgene and a K18 simple epithelial keratin transgene in the epidermis of mice null for K14. Under conditions where the hybrid epidermal keratin restored a wild-type phenotype to newborn epidermis, K18 partially but not fully rescued. The explanation does not appear to reside in an inability of K18 to form 10-nm filaments with K5, which it does in vitro and in vivo. Rather, it appears that the keratin network formed between K5 and K18 is deficient in withstanding mechanical stress, leading to perturbations in the keratin network in regions of the skin that are subjected either to natural or to mechanically induced trauma. Taken together, these findings suggest that the loss of a type I epidermal keratin cannot be fully compensated by its counterpart of simple epithelial cells, and that in vivo, all keratins are not equivalent.Keywords
This publication has 56 references indexed in Scilit:
- Directed Expression of Keratin 16 to the Progenitor Basal Cells of Transgenic Mouse Skin Delays Skin MaturationThe Journal of cell biology, 1998
- A Proline Residue in the α-Helical Rod Domain of Type I Keratin 16 Destabilizes Keratin HeterotetramersJournal of Biological Chemistry, 1997
- Chronic hepatitis, hepatocyte fragility, and increased soluble phosphoglycokeratins in transgenic mice expressing a keratin 18 conserved arginine mutant.The Journal of cell biology, 1995
- Dynamics of human keratin 18 phosphorylation: polarized distribution of phosphorylated keratins in simple epithelial tissues.The Journal of cell biology, 1995
- Ultrastructural Identification of Basic Abnormalities as Clues to Genetic Disorders of the EpidermisJournal of Investigative Dermatology, 1994
- Ultrastructural Identification of Basic Abnormalities as Clues to Genetic Disorders of the Epidermis.Journal of Investigative Dermatology, 1994
- Identification of the major physiologic phosphorylation site of human keratin 18: potential kinases and a role in filament reorganization.The Journal of cell biology, 1994
- INTERMEDIATE FILAMENTS: Structure, Dynamics, Function and DiseaseAnnual Review of Biochemistry, 1994
- Ectopic synthesis of epidermal cytokeratins in pancreatic islet cells of transgenic mice interferes with cytoskeletal order and insulin production.The Journal of cell biology, 1993
- Comparison of mouse and human keratin 18: A component of intermediate filaments expressed prior to implantationDifferentiation, 1986