Original Article

Insights into the Dynamic Properties of Keratin Intermediate Filaments in Living Epithelial Cells

Correspondence to: Robert D. Goldman, Dept. of Cell and Molecular Biology, Northwestern Medical School, 303 E. Chicago Ave., Ward 11-145, Chicago, IL 60611. Tel:(312) 503-4215 Fax:(312) 503-0954 E-mail:r-goldman{at}northwestern.edu.

The properties of keratin intermediate filaments (IFs) have been studied after transfection with green fluorescent protein (GFP)-tagged K18 and/or K8 (type I/II IF proteins). GFP-K8 and -K18 become incorporated into tonofibrils, which are comprised of bundles of keratin IFs. These tonofibrils exhibit a remarkably wide range of motile and dynamic activities. Fluorescence recovery after photobleaching (FRAP) analyses show that they recover their fluorescence slowly with a recovery t_1/2 of 100 min. The movements of bleach zones during recovery show that closely spaced tonofibrils (<1 µm apart) often move at different rates and in different directions. Individual tonofibrils frequently change their shapes, and in some cases these changes appear as propagated waveforms along their long axes. In addition, short fibrils, termed keratin squiggles, are seen at the cell periphery where they move mainly towards the cell center. The motile properties of keratin IFs are also compared with those of type III IFs (vimentin) in PtK2 cells. Intriguingly, the dynamic properties of keratin tonofibrils and squiggles are dramatically different from those of vimentin fibrils and squiggles within the same cytoplasmic regions. This suggests that there are different factors regulating the dynamic properties of different types of IFs within the same cytoplasmic regions.

Key Words: keratin, tonofibrils, squiggles, dynamics, motility

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