Mutation in keratin 18 induces mitochondrial fragmentation in liver-derived epithelial cells

H Kumemura, M Harada, C Yanagimoto, H Koga… - Biochemical and …, 2008 - Elsevier
H Kumemura, M Harada, C Yanagimoto, H Koga, T Kawaguchi, S Hanada, E Taniguchi…
Biochemical and biophysical research communications, 2008Elsevier
Microtubules (MTs) and microfilaments (MFs) are known to modulate mitochondrial
morphology, distribution and function. However, little is known evidence about the role of
intermediate filaments (IFs) in modulating mitochondria except desmin. To investigate
whether or not the IFs regulate mitochondrial morphology, distribution, and function, we
manipulated the IFs of cultured epithelial cells to express a mutant keratin 18 (K18). In
contrast to the filamentous expression of wild K18, mutant K18 induced aggregation of …
Microtubules (MTs) and microfilaments (MFs) are known to modulate mitochondrial morphology, distribution and function. However, little is known evidence about the role of intermediate filaments (IFs) in modulating mitochondria except desmin. To investigate whether or not the IFs regulate mitochondrial morphology, distribution, and function, we manipulated the IFs of cultured epithelial cells to express a mutant keratin 18 (K18). In contrast to the filamentous expression of wild K18, mutant K18 induced aggregation of K8/18, showing no fine IF network in the cells. In mutant K18-transfected cells, the mitochondria were fragmented into small spheroids, although they were observed as mitochondrial fibers in un-transfected or wild K18-transfected cells. Fluorescence recovery after photobleaching of fluorescence-labeled mitochondria was markedly less in the mutant K18-transfected cells, although a significant recovery was confirmed in wild K18-transfected cells. These findings suggest that the IFs are important for the maintenance of normal mitochondrial structures.
Elsevier