Jäger Stefanie, Bucci Cecilia, Tanida Isei, Ueno Takashi, Kominami Eiki, Saftig Paul, Eskelinen Eeva-Liisa
Institute of Biochemistry, University of Kiel, Olshausenstr. 40, 24098 Kiel, Germany.
J Cell Sci. 2004 Sep 15;117(Pt 20):4837-48. doi: 10.1242/jcs.01370. Epub 2004 Aug 31.
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.
小GTP结合蛋白Rab7在晚期内吞途径和溶酶体生物发生中发挥作用。然而,哺乳动物Rab7在自噬中的作用尚不清楚。我们通过RNA干扰抑制Rab7功能以及过表达显性负性Rab7来解决这个问题。我们在此表明,Rab7是形成优选位于核周的大聚集体所必需的,自噬体标志物LC3与Rab7以及晚期内体和溶酶体标志物共定位。通过电子显微镜我们表明,这些大聚集体对应于围绕晚期内体或溶酶体小泡的自噬泡。我们的定量电子显微镜实验表明,Rab7对于早期自噬体向晚期自噬泡的初始成熟不是必需的,但它参与晚期自噬泡的最终成熟。最后,我们表明,在溶酶体膜蛋白Lamp1和Lamp2缺陷的细胞中,Rab7向自噬泡的募集受到阻碍,我们最近表明这些细胞在饥饿期间会积累晚期自噬泡。总之,我们的结果表明Rab7在晚期自噬泡的最终成熟中发挥作用。