Endoplasmic reticulum–endosome contact increases as endosomes traffic and mature

Jonathan R. Friedman, Jared R. DiBenedetto, Matthew West, Ashley A. Rowland, Gia K. Voeltz

Molecular Biology of the Cell · 2013 · 321 citations · 26 references

Concepts

TL;DR

The endosomal pathway mediates plasma membrane cargo uptake, sorting, and lysosome targeting, and its maturation requires precise spatiotemporal recruitment of factors, microtubule‑mediated trafficking, and contact with the endoplasmic reticulum, yet the frequency, dynamics, and physical attributes of these ER–endosome contacts remain poorly understood. The study investigates how ER tubules interact with endosomes during trafficking and maturation. High‑resolution 3‑D electron microscopy was used to show that ER tubules wrap around endosomes and that both organelles contact microtubules at or near membrane contact sites. During trafficking, endosomes stay bound to the ER, prompting the ER to reorganize around them, and as they mature they become increasingly tightly associated, indicating that endosome maturation and trafficking occur while coupled to the ER membrane.

Abstract

The endosomal pathway is responsible for plasma membrane cargo uptake, sorting, and, in many cases, lysosome targeting. Endosome maturation is complex, requiring proper spatiotemporal recruitment of factors that regulate the size, maturity, and positioning of endosomal compartments. In animal cells, it also requires trafficking of endosomes on microtubules. Recent work has revealed the presence of contact sites between some endosomes and the endoplasmic reticulum (ER). Although these contact sites are believed to have multiple functions, the frequency, dynamics, and physical attributes of these contacts are poorly understood. Here we use high-resolution three-dimensional electron microscopy to reveal that ER tubules wrap around endosomes and find that both organelles contact microtubules at or near membrane contact sites. As endosomes traffic, they remain bound to the ER, which causes the tubular ER to rearrange its structure around dynamic endosomes at contact sites. Finally, as endosomes transition through steps of maturation, they become more tightly associated with the ER. The major implication of these results is that endosomes mature and traffic while coupled to the ER membrane rather than in isolation.

References

26