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. 2016 Sep 13;5:e18605. doi: 10.7554/eLife.18605

Figure 7. Interplay between ATL and the reticulons.

(A) Peripheral ER network in a U2OS cell expressing GFP-calreticulin under the endogenous promoter in wild type cells or in cells stably expressing mCherry-tagged Rtn4a. The bottom row shows three time points. Stationary pixels appear white, while those moving appear in colors. Scale bar = 10 µm. (B) As in (A), but with a higher expression level of mCherry-Rtn4a, resulting in unbranched tubules. (C) As in (B), but showing a cell with fragmented ER. (D) As in (B), but with cells that also stably express GFP-ATL-1 or GFP-ATL-3. (E) As in (B), but with cells that also express a GTPase defective ATL-1 mutant (GFP-ATL-1 K80A). The second column shows three time points for both the ATL and Rtn channels. Stationary pixels appear white, while those moving appear in colors. Scale bar = 10 µm.

DOI: http://dx.doi.org/10.7554/eLife.18605.018

Figure 7.

Figure 7—figure supplement 1. Co-overexpression of ATL mutants and Rtn4a in U2OS cells.

Figure 7—figure supplement 1.

(A) Peripheral ER network in a U2OS cell expressing a high level of mCherry-tagged Rtn4a and GFP-ATL-1 R217Q, a dimerization defective mutant. Scale bar = 10 µm. (B) Peripheral ER network in a U2OS cell expressing a high level of mCherry-tagged Rtn4a and GFP-ATL-1 K80A, a GTPase defective mutant. The second column shows three time points for both the ATL and Rtn channels. Stationary pixels appear white, while those moving appear in colors. Scale bar = 10 µm.