The organization of intermediate filaments in cultured epithelial cells was rapidly and radically affected by intracellularly injected monoclonal antikeratin filament antibodies. Different antibodies had different effects, ranging from an apparent splaying apart of keratin filament bundles to the complete disruption of the keratin filament network. Antibodies were detectable within cells for more than four days after injection. The antibody-induced disruption of keratin filament organization had no light-microscopically discernible effect on microfilament or microtubule organization, cellular morphology, mitosis, the integrity of epithelial sheets, mitotic rate, or cellular reintegration after mitosis. Cell-to-cell adhesion junctions survived keratin filament disruption. However, antibody injected into a keratinocyte-derived cell line, rich in desmosomes, brought on a superfasciculation of keratin filament bundles, which appeared to pull desmosomal junctions together, suggesting that desmosomes can move in the plane of the plasma membrane and may only be 'fixed' by their anchoring to the cytoplasmic filament network. Our observations suggest that keratin filaments are not involved in the establishment or maintenance of cell shape in cultured cells.
Skip Nav Destination
Article navigation
1 February 1983
Article|
February 01 1983
Morphology, behavior, and interaction of cultured epithelial cells after the antibody-induced disruption of keratin filament organization.
M W Klymkowsky
R H Miller
E B Lane
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1983) 96 (2): 494–509.
Citation
M W Klymkowsky, R H Miller, E B Lane; Morphology, behavior, and interaction of cultured epithelial cells after the antibody-induced disruption of keratin filament organization.. J Cell Biol 1 February 1983; 96 (2): 494–509. doi: https://doi.org/10.1083/jcb.96.2.494
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Email alerts
Advertisement
Advertisement