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First published online 31 August 2004
doi: 10.1242/jcs.01370


Journal of Cell Science 117, 4837-4848 (2004)
Published by The Company of Biologists 2004
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Research Article

Role for Rab7 in maturation of late autophagic vacuoles

Stefanie Jäger1, Cecilia Bucci2, Isei Tanida3, Takashi Ueno3, Eiki Kominami3, Paul Saftig1 and Eeva-Liisa Eskelinen1,*

1 Institute of Biochemistry, University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany
2 Dipartimento di Scienze e Tecnologie Biologiche ed Ambientali, Universita degli Studi di Lecce, 73100 Lecce, Italy
3 Department of Biochemistry, Juntendo University School of Medicine, 2-1-1, Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan

* Author for correspondence (e-mail: eleskelinen{at}biochem.uni-kiel.de)

Accepted 17 June 2004

The small GTP binding protein Rab7 has a role in the late endocytic pathway and lysosome biogenesis. The role of mammalian Rab7 in autophagy is, however, unknown. We have addressed this by inhibiting Rab7 function with RNA interference and overexpression of dominant negative Rab7. We show here that Rab7 was needed for the formation of preferably perinuclear, large aggregates, where the autophagosome marker LC3 colocalised with Rab7 and late endosomal and lysosomal markers. By electron microscopy we showed that these large aggregates corresponded to autophagic vacuoles surrounding late endosomal or lysosomal vesicles. Our experiments with quantitative electron microscopy showed that Rab7 was not needed for the initial maturation of early autophagosomes to late autophagic vacuoles, but that it participated in the final maturation of late autophagic vacuoles. Finally, we showed that the recruitment of Rab7 to autophagic vacuoles was retarded in cells deficient in the lysosomal membrane proteins Lamp1 and Lamp2, which we have recently shown to accumulate late autophagic vacuoles during starvation. In conclusion, our results showed a role for Rab7 in the final maturation of late autophagic vacuoles.

Key words: Autophagy, Rab7, LC3, Lysosome, Endosome, RNA interference, LAMP deficiency, Electron microscopy


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