RESEARCH      PUBLICATIONS      MOVIE GALLERY      TEAM      CONTACT

Identification of novel principles of keratin filament network turnover in living cells

Windoffer R, Wöll S, Strnad P, Leube RE, 2004

It is generally assumed that turnover of the keratin filament system occurs by exchange of subunits along its entire length throughout the cytoplasm. We now present evidence that a circumscribed submembranous compartment is actually the main site for network replenishment. This conclusion is based on the following observations in living cells synthesizing fluorescent keratin polypeptides:


1) Small keratin granules originate in close proximity to the plasma membrane and move toward the cell center in a continuous motion while elongating into flexible rod-like fragments that fuse with each other and integrate into the peripheral KF network.


2) Recurrence of fluorescence after photobleaching is first seen in the cell periphery where keratin filaments are born that translocate subsequently as part of the network toward the cell center.


3) Partial keratin network reformation after orthovanadate-induced disruption is restricted to a distinct peripheral zone in which either keratin granules or keratin filaments are transiently formed.


These findings extend earlier investigations of mitotic cells in which de novo keratin network formation was shown to originate from the cell cortex. Taken together, our results demonstrate that the keratin filament system is not homogeneous but is organized into temporally and spatially distinct subdomains. Furthermore, the cortical localization of the regulatory cues for keratin filament turnover provides an ideal way to adjust the epithelial cytoskeleton to dynamic cellular processes.

Time-lapse epifluorescence microscopy of confluent PK18-5 cells depicting continuous inward flow of keratin filament fluorescence from the entire cell circumference. Recording intervals: 30 s.


Download: .mp4 / .wmv

Time-lapse epifluorescence microscopy of peripheral free edge of a PK18-5 cell showing centripetal flow of HK18-YFP fluorescence originating in a submembraneous compartment and resulting in integration into the peripheral filament network. Recording intervals: 30 s.


Download: .mp4 / .wmv

Time-lapse confocal laser scanning microscopy of a peripheral free region of a human primary keratinocyte depicting the inward-directed aviement of HK14-YFP fluorescence which originates in a submembraneous compartment and results in integration of rod-like structures into the peripheral filament network. Recording intervals: 60 s.


Download: .mp4 / .wmv

Time-lapse confocal laser scanning microscopy of a peripheral free region of a human primary keratinocyte depicting the inward-directed aviement of HK14-YFP fluorescence which originates in a submembraneous compartment and results in integration of rod-like structures into the peripheral filament network. Recording intervals: 60 s.


Download: .mp4 / .wmv

Time-lapse epifluorescence microscopy of a peripheral region of a SW13 cell producing fluorescent keratins HK8-CFP and HK18-YFP highlighting details of keratin filament formation beneath the plasma membrane (top). Recording of EYFP-elicited fluorescence was every 30 s.


Download: .mp4 / .wmv

Time-lapse fluorescence imaging of a FRAP experiment, in which a section of a PK18-5 cell producing HK18-YFP was bleached, demonstrating that filamentous fluorescence recovery occurs preferentially in the cell periphery. Recording intervals, 2 min.


Download: .mp4 / .wmv

Time-lapse fluorescence image series depicting the distribution of HK13-EGFP in AK13-1 cells after a short treatment with orthovanadate (10 mM, 4 min). Recording intervals, 15 s.


Download: .mp4 / .wmv

Time-lapse imaging of HK13-EGFP fluorescence (inverse presentation) in a peripheral region of an AK13-1 cell in the continued presence of orthovanadate (10 mM). Images were recorded every 30 s.


Download: .mp4 / .wmv

Time-lapse fluorescence imaging of a peripheral part of a desmosome-free A-431 cells stably synthesizing a dominant-negative connexin-desmoglein chimera and producing HK13-EGFP after cDNA-transfection. Recording intervals, 30 s.


Download: .mp4 / .wmv