- Research article
- Open Access
Direct observation of molecular arrays in the organized smooth endoplasmic reticulum
© Korkhov and Zuber; licensee BioMed Central Ltd. 2009
- Received: 23 March 2009
- Accepted: 24 August 2009
- Published: 24 August 2009
Tubules and sheets of endoplasmic reticulum perform different functions and undergo inter-conversion during different stages of the cell cycle. Tubules are stabilized by curvature inducing resident proteins, but little is known about the mechanisms of endoplasmic reticulum sheet stabilization. Tethering of endoplasmic reticulum membranes to the cytoskeleton or to each other has been proposed as a plausible way of sheet stabilization.
Here, using fluorescence microscopy we show that the previously proposed mechanisms, such as membrane tethering via GFP-dimerization or coiled coil protein aggregation - do not explain the formation of the calnexin-induced organized smooth endoplasmic reticulum membrane stacks. We also show that the LINC complex proteins known to serve a tethering function in the nuclear envelope are excluded from endoplasmic reticulum stacks. Finally, using cryo-electron microscopy of vitreous sections methodology that preserves cellular architecture in a hydrated, native-like state, we show that the sheet stacks are highly regular and may contain ordered arrays of macromolecular complexes. Some of these complexes decorate the cytosolic surface of the membranes, whereas others appear to span the width of the cytosolic or luminal space between the stacked sheets.
Our results provide evidence in favour of the hypothesis of endoplasmic reticulum sheet stabilization by intermembrane tethering.
- Endoplasmic Reticulum
- Endoplasmic Reticulum Membrane
- Endoplasmic Reticulum Protein
- Multilamellar Body
- Tether Complex
A key function of most cellular membranes is to form organelles enclosing biochemically distinct subcompartments in the cell essential for a multitude of cellular processes. The endoplasmic reticulum (ER) comprises the most abundant and highly versatile component of the endomembrane system. The specialized sub-compartments of the ER include: (i) the nuclear envelope (NE), composed of two adjacent membrane sheets surrounding the nucleus, and (ii) the peripheral ER, including membrane sheets and a complex network of tubules [1, 2]. ER has traditionally been classified into rough and smooth, based on early electron microscopy observations, where the rough ER was distinguished by the presence of ribosomes on its surface, and the smooth one by their absence .
The overall architecture of the ER is highly evolutionarily conserved from yeast to mammals, with luminal intermembrane distances ranging between 50 and 100 nm . Inter-conversion between tubes and sheets of ER has been proposed based on their varying abundance during various stages of cell cycle . This clearly indicated that active components are involved in shaping the ER. In line with this suggestion, proteins such as the reticulons and DP1, that induce high membrane curvature and thus stabilize ER tubes, have recently been identified [6, 7].
In contrast, the mechanism of ER sheet stabilization has been elusive and the identities of the proteins involved are unknown. Several protein complexes have been proposed to stabilize and sustain the extended flat double sheet morphology of the nuclear envelope, such as the SUN proteins that span the whole width of the NE lumen, connecting the nucleus to the cytoskeleton via Nesprin family proteins . The peripheral ER sheets may be stabilized by tethering to the cytoskeleton by, for example, Climp63, which is a microtubule-binding protein [1, 4, 9]. Weak interactions between fluorescent protein tags engineered onto ER-resident proteins, such as cytochrome b(5) or Sec61, have been proposed to stabilize ER sheet morphology and to induce formation of organized smooth ER, OSER [10, 11]. A range of morphologies, including cubic [10, 12], tubular  and stacked sheet OSER have been identified, based on electron microscopy. Because of the highly ordered arrangement of these large membranous assemblies, it has been suggested that OSER may serve as a paradigm for membrane and organelle biogenesis at molecular level .
While working on interactions of ER chaperones with neurotransmitter transporters, we found that overexpression of calnexin, an ER-resident lectin chaperone with a single transmembrane-spanning domain, induces formation of stacked OSER membranes, detected by fluorescence and cryo-electron microscopy . We have also detected OSER membranes in untransfected mammalian cells, by immunocytochemical labelling of endogenous calnexin . These structures are highly dynamic and contain mobile, non-aggregated membrane protein pools [10, 11, 15]. OSER-like membrane structures have been observed previously in certain pathological conditions in vivo, e.g., in Emery-Dreifuss disease, torsion dystonia and Hodgkin's lymphoma [16–18]. Thus, OSER membrane expansion in eukaryotic cells may represent a physiologically relevant response of cells to stress, i.e., excessive production of misfolded or misassembled proteins. Such response mechanistically resembles the ER stress-induced ER expansion in yeast, where sequestration of the ER membranes into autophagosome-like multilamellar structures, but not their autophagic degradation, is essential for survival . This suggestion is corroborated by the observation that OSER structures induced in mammalian cells are not subject to bulk degradation via lysosomes/autophagosomes .
Here, we revisit the mechanisms of ER sheet stabilization and stacking and present a detailed investigation into the organization of the stacked smooth ER sheets. Our results indicate that the OSER membrane stacks are highly regular structures that may be maintained through the ordered tethering of membranes by a large native complex, rather than through interactions between heterologously overexpressed proteins.
Reagents, and cell lines and DNA constructs
DMEM and standard cell-culture reagents were from GIBCO (Paisley, UK). SUN1 and SUN2 antibodies were a generous gift from Sue Shackleton (Leicester, UK); Nesprin-1 antibody was from Abcam (Cambridge, UK). Anti-rabbit antibody conjugated with Texas Red was from Invitrogen (Paisley, UK). Climp63-GFP construct was generously provided by Hans-Peter Hauri (Basel, Switzerland). Calnexin constructs were described previously .
HEK293 cells were cultured at 37°C, supplemented with 5% CO2. Transfections were performed using Lipofectamine-2000 (Invitrogen), according to supplier's instructions. A total of 2-4 μg of plasmid DNA were used in an individual transfection reaction per 3 cm plate; 10 μg of plasmid DNA were used to transfect cells growing in 10 cm dishes.
For confocal microscopy cells were grown on poly-L-glutamine-coated (Sigma) glass cover-slips until 50-80% confluence, followed by transfection and/or fixation. Cells were fixed with 4% paraformaldehyde (Sigma) in phosphate-buffered saline (PBS), permeabilized for 30 min at room temperature using PBS with 1% BSA and 0.01% Triton-X100 and stained for 1 h with primary and secondary antibodies (in PBS, 1% BSA) where appropriate. Coverslips with stained cells were washed four times in PBS and mounted onto glass slides in Vectashield medium (Vector Laboratories) for microscopy. Images were acquired using Zeiss LSM 510 confocal microscope with a 63× objective lens.
Cryo-electron microscopy of vitreous sections
The procedure of cell preparation for cryo-electron microscopy of vitreous sections (CEMOVIS) was described previously . Briefly, cells were centrifuged for 5 min at 1400 rpm and resuspended in 30% dextran-PBS (average mass of dextran - 40 kDA; Sigma-Aldrich, Buchs, Switzerland). The cells were introduced into the 200-μm deep cavity of a copper membrane carrier (Leica, Vienna, Austria) and vitrified by high pressure freezing with a Leica EMPACT2 apparatus. Membrane carriers were clamped in the specimen holder of an FC6/UC6 cryo-ultramicrotome (Leica) and trimmed in pyramidal shape. Copper was trimmed away with a diamond knife (Diatome, Bienne, Switzerland) on part of the specimen holder and the specimen was trimmed to pyramidal shape with the same knife. 50-nm feed cryosections were cut with 35° diamond knife (Diatome) under standard cutting conditions, at -140°C. The cryosections were collected on 1000-mesh grids (Agar Scientific, Essex, United Kingdom) coated with carbon and stored in liquid nitrogen or transferred immediately to the microscope. The images were acquired with Tecnai T12 microscope (FEI Company, Eindhoven, Netherlands) on film, under standard low-dose imaging conditions, using 26,000-30,000× magnification, at -1.5 to -2.5 μm defocus and 120 kV.
Images were scanned and digitised using an MRC KZA scanner at pixel size of 2 or 2.3 Å, dependent on magnification during cryo-EM experiments. All image analysis - selection of the regions of interest, distance measurements, Fourier transformation, identification of strong reflections - was performed using Ximdisp . For measurement of the intermembrane distances, the micrographs showing OSER membrane stacked parallel (13 micrographs) and perpendicular (4 micrographs) to the cutting direction, respectively. The distances between the middle points of the juxtaposed membrane sheets were measured in the areas of interest where the stacked membranes were parallel to each other. The distance measurements in stacks perpendicular to the cutting direction were unaffected by specimen compression during the cutting procedure; the comparisons of the parallel vs perpendicular cytosolic distances, which showed relatively small S.D. values, revealed an approximately 30% compression of the specimen due to cutting. MRC Image2000 software programs TRMASK and FFTRANS  were used for masking and Fourier transformation/filtered image calculation, respectively. Briefly, well-preserved regions of interest were boxed and rotated to align the membranes vertically. Fourier transforms were calculated and strong reflections, including the equatorial data, were masked. To visualize the features of interest, the filtered images were calculated using the masked Fourier transforms.
Inspection of the images confirmed that appearance of strong reflections in the selected regions of interest does not correlate with the direction of the knife marks (data not shown). The artefacts caused by the diamond knife - knife marks and crevasses (normally perpendicular to each other) - in most cases result in appearance of very low resolution reflections (250-350 Å), outside the range where we observed ordered features (40-100 Å). Image analysis was performed on images devoid of crevasses.
Fluorescent protein tag oligomerization does not cause ER stacking
We have previously shown that calnexin-YFP or calnexin-CFP overexpression causes OSER expansion, based on immunofluorescence and low-magnification CEMOVIS images ; we also observed OSER-like inclusion in non-transfected mammalian cells by staining for endogenous calnexin . In contrast, the findings of Snapp et al. (2003) suggested that GFP-tagged membrane proteins residing in the proximal ER membranes could weakly interact with each other, causing the membranes to stack . This stacking was proposed to be mediated either via interactions between the intrinsic extramembranous domains of the ER proteins, or by self-association of the fluorescent protein tags. OSER induction in the case of GFP-tagged proteins was abolished when non-oligomerizing GFP mutants were used .
Climp63 is excluded from OSER
Another hypothesis of ER sheet stabilization and stacking involved Climp63, a microtubule-binding ER protein . Climp63 contains an extended luminal coiled-coil domain, and upon purification forms large rod-shaped aggregates. These structures appear sufficiently long to span ER lumen, and thus could be the prime candidates for ER sheet stabilization and stacking.
We co-expressed calnexin-CFP with Climp63-GFP in HEK293 cells. No colocalization of the two proteins in the OSER could be observed (Figure 1B); Climp63-GFP was completely excluded from the calnexin-positive multilamellar bodies. This suggested that Climp63-GFP does not participate in stabilization of the OSER stacks.
LINC complex proteins are not involved in OSER stacking
Some of the OSER compartments were previously suggested to be derived from NE membranes [10, 12], making the involvement of the NE-stabilizing proteins in OSER plausible. Proteins of the NE that participate in the so-called LINC complex, SUN1 and SUN2, span the entire width of the NE connecting NE inner membrane with NE outer membrane . High levels of over-expressed ER proteins essential for production, folding and assembly of membrane proteins could perturb the normal biogenesis of SUN proteins leading to their 'leakage' into the peripheral ER instead of the NE, inducing ER membrane stacking. Thus, a possible explanation for OSER induction by ER protein overexpression could be their effect on targeting of SUN proteins.
To test this hypothesis, we used immuno-fluorescence to visualize the endogenous SUN proteins in cells overexpressing calnexin. Antibody staining of SUN1 and SUN2 revealed the presence of SUN proteins in the NE, partially colocalizing with calnexin-CFP (Figure 1C and 1D). However, similarly to Climp63-GFP, endogenous SUN proteins were excluded from the calnexin-induced OSER structures.
We have also tested whether endogenous Nesprin-1 enters the multilamellar bodies. Proteins of the Nesprin family include several giant isoforms (M.W. up to 1 MDa) with large cytosolic regions. The classical function of Nesprins is to link the nuclear envelope to actin cytoskeleton [8, 24]. Cytosolic regions of Nesprins contain spectrin repeats that may undergo oligomerization. Thus, Nesprins could fulfil the criteria for tethering of ER membranes and inducing the OSER stacks. However, similarly to SUN proteins, we found Nesprin-1 to be excluded from calnexin-CFP stained OSER structures (Figure 1E). Based on these experiments, involvement of LINC complex-participating proteins (SUN1-2 and Nesprin-1) in OSER biogenesis was ruled out.
Cryo-electron microscopy of vitreous sections reveals periodicity of OSER membrane packing
To obtain a more detailed view of the ER membrane stack organization, we performed a CEMOVIS analysis of HEK293 cells over-expressing YFP-tagged calnexin. CEMOVIS is a method that preserves the native structure of the cell and allows imaging of the cellular architecture at the molecular level . We have used this method previously to show that calnexin-induced OSER structures are indeed multilamellar .
The long distances between cytosolic and luminal faces of the membranes clearly indicated that overexpressed proteins on their own would not be able to stabilize the OSER. Calnexin, even tagged with a fluorescent protein (the length of the YFP barrel is ~4 nm) on its cytosolic C-terminus (90 amino acid residues), would not be able to reach out and connect two ER membranes. Likewise, the length of the luminal domain of calnexin, based on its X-ray structure , is insufficient to bridge the juxtaposed OSER membranes.
CEMOVIS reveals macromolecular arrays within OSER
Molecular arrays tethering stacked ER sheets
The high regularity of the ER membrane stacks suggested that tethering complexes could exist. A mechanism similar to that by which coiled-coil proteins organize Golgi membrane stacks  could account for ER sheet stabilization and stacking. We set out to perform a more in-depth analysis of our CEMOVIS images to detect the presence of molecular tethers between adjacent stacked membranes.
The images obtained by CEMOVIS are very noisy, allowing only the gross features, such as membranes or large protein complexes (e.g., ribosomes and microtubules), to be observed directly. Visualization of smaller objects directly is, in most instances, not possible. However, if the molecules are arranged in an orderly fashion, this can be detected in Fourier space and, if the order is sufficiently good, the structures of the arrayed molecules can be determined to near atomic resolution in favourable cases, e.g., from 2D crystals of membrane proteins . We therefore analyzed the images in Fourier space, as described below.
The image analysis routine included digitization of the micrographs and selection of well-preserved regions of interest (as shown in Figure 3C). We excluded micrograph areas in which the tilt angle of the membranes relative to the section plane was strongly deviating from 90°, as well as the areas where the specimen was severely damaged by freezing and cryo-sectioning procedures (e.g. where crystalline ice and/or crevasses were observed). Selected regions of interest included two membranes and an intermembrane space (either luminal or cytosolic). Fourier transforms of the boxed regions were calculated and inspected for the presence of strong reflections along or at an angle to the meridian (as in Figure 3D), which would be indicative of an ordered density pattern within the analysed area.
To exclude the possibility of an artefact caused by sample preparation or imaging, 3 adjacent areas of the same image were analysed as described above (Figure 3E). Only the middle region of interest (region "2") showed a reflection at 56 Å-1, whereas the regions on either side of region "2" showed no ordered densities above the noise level. This indicated that the features detected in region "2" are not extending over a large area of the micrograph, but are confined to the region of interest between the membranes. The same image also illustrates a distinction between orientation of the striations between the membranes (indicated by white lines within the boxed region "2") and the cutting direction (indicated by an open arrow). We found no correlation between the cutting direction and the observed ordered densities in the best images, suggesting that these features are not created during sample preparation (data not shown).
Based on our selection criteria, in a total of 55 micrographs, we found 17 reasonably well-ordered regions on the cytosolic side (Figure 4A-D) and 4 reasonably well-ordered regions of interest on the luminal side (Figure 4E) connecting two adjacent OSER membranes. The densities that were visualized between the OSER membranes were represented by the sets of parallel striations, at an angle to the two ER membranes. The period and angle of striations in the luminal and cytosolic regions were similar: although in some cases the striations were at an approximately 90° angle to the plane of the membrane (Figure 4A), in others the angle was sharper (Figures 4B-E; the angles observed in all images are plotted in Figure 4F). In several cases discontinuities in the ordered regions were observed, as in Figure 4C, where such feature coincides with an apparent broadening of the intermembrane distance. Although the sampling of the luminal regions of interest was limited (n = 4), the average observed luminal inter-striation spacing appeared similar to the cytosolic one (Figure EA). We found no correlation between the intermembrane distances and the striation/membrane incident angles (Figure 4F).
The observation of densely packed, periodic structures connecting two ER membranes suggests that these structures may act as molecular tethers. An absence of correlation between the parameters of these tethers, namely the spacing, the angle and the distance between the membranes, is indicative of high flexibility of these tethering complexes, which in turn is in line with the previously suggested dynamic nature of the proteinaceous matrix that shapes the ER .
To the best of our knowledge, this is the first report detailing ER membrane sheet organization in a native environment, i.e. unfixed, hydrated cells. To date, the reports of attempts to visualize the ultrastructure of the ER membranes included freeze fracture electron microscopy of the crystalloid ER (tubular OSER) in the UT-1 cells, which showed macromolecular complexes of approximately 10 nm in diameter , and a freeze fracture/deep etch electron microscopy analysis of endomembranes of various cells, which revealed existence of 'bridges' connecting the membranes of different organelles . However, both reports had common problems inherent to the employed methodology: the electron microscopy was performed on the dehydrated and/or fixed specimen, after shadowing with platinum and carbon - the replicas were subjected to imaging. This implies that the observed structures could be artefacts, e.g. due to aggregation of material during the etching process, demeaning the value of those observations.
We used CEMOVIS methodology to preserve the native ultrastructure and to image the intracellular membranes of the HEK293 cells by cryo-EM at unprecedented level of detail. A sub-compartment of ER, OSER, was used as a model system, which allowed us to sample a sufficient amount of stacked ER sheet micrographs for analysis. Using projection images of the OSER membranes we have identified ordered cytosolic and luminal macromolecular arrays supporting ER membrane stacking. The imaging of the OSER membranes may not allow us to measure directly the interaction between OSER membranes and thus we may not unequivocally rule out the possibility that the ordering of the molecules is secondary to ER stack formation. However, we propose that the OSER membranes may be stabilized by these arrays.
We have shown that induction of ER sheet stacks by YFP-tagged calnexin overexpression is not driven by fluorescent protein dimerization. Monomeric fluorescent protein-tagged calnexin induces OSER formation; the stacked membranes are too far apart for direct in trans interaction between overexpessed proteins. It is unlikely that the discrepancy between our results and those published previously  resulted from usage of different cell types, cell culture conditions, reagents and DNA constructs. Mammalian cells were used throughout and similar vectors were used for transfections in both studies; the proteins employed to induce OSER (cytochrome b(5), Sec61 and calnexin ) are known to exist in a complex with each other , and are therefore likely to reside in the same compartments. In addition, OSER-like structures have been observed in mammalian cells in the absence of any protein overexpression, with or without GFP involved . It is possible that under certain circumstances, depending on the structure of a particular fusion construct, the presence of GFP may indeed be conducive to trans-interaction between the ER membranes leading to membrane tethering. It is worth noting that a broad range of ER-localized proteins have been known to induce OSER formation, including: cytochrome b5 , HMG-CoA reductase , inositol 1,4,5-trisphosphate receptor , cytochrome P-450 , microsomal aldehyde dehydrogenase , torsinA  and others. Therefore, it can be anticipated that more than one element in the structure of these very different proteins should affect their ability to cause rearrangements in the ER ultrastructure.
Several intracellular compartments, both in prokaryotes and eukaryotes, have been studied by CEMOVIS previously with a comparable level of detail [35–41]. Ordered arrangement of trans-cleft molecular complexes in the neuronal synapses has been visualized using this technique . Recently published tomographic reconstruction of desmosomal vitreous sections revealed quasi-crystalline arrays of cadherin molecules connecting the skin cells [25, 43]. We propose a model whereby OSER membranes are stabilized in a similar way, i.e., adjacent ER membranes are connected by extended arrays of intracellular 'adhesion' molecules, although our results indicate that the OSER-stabilizing structures are more disordered, compared to the highly organized arrays of the desmosomes .
A number of questions remain open, the most important being the identity of the proteins involved in OSER stabilization. We have ruled out the obvious candidates, represented by the coiled-coil domain-containing Climp63, and the LINC complex proteins that have been proposed to perform a similar role in the NE. This shows that, although the OSER membranes may originate from the NE at least in some cases [10, 12], the molecular machinery involved in OSER stabilization is likely different from that specialized in NE maintenance. Because the ordered areas could be observed between both luminal and cytosolic ER membrane faces, it is possible that more than one protein component may be involved in ER stacking interactions. It is possible that proteins involved are not integral membrane proteins, as is the case with the members of GRASP family (e.g., GRASP65), which are peripherally inserted into the Golgi membranes and stack the Golgi cisterns upon oligomerization [44–47]. Also, it remains to be determined whether the formation of the OSER stacks is primed by the interactions between adjacent ER membranes via the ordered macromolecular complexes, or whether the protein crowding and array formation is preceded by the formation of a membrane stack, which is in turn brought about by an independent mechanism.
Our results support a hypothesis according to which active maintenance of organized smooth ER (and, by extension, the regular ER sheets) may be achieved in part by molecular tethering complexes. The potential significance of our findings is underscored by the recently shown cell cycle dependent 'tug of war' between sheet and tubular ER morphologies . It is obvious that the molecules involved in ER sheet stabilization and stacking, together with structural proteins that act to stabilize the tubular ER morphology, e.g. reticulons and DP1 , must play key roles in the ER remodelling. Identification of the ER sheet stabilizing and tethering proteins, called for by the findings presented here, would help us understand the relationship between the ER morphologies, the cell cycle and the various pathologies that affect them.
We thank Christopher G. Tate and Nigel Unwin for support. We are also thankful to Sean Munro and Francesca Magnani for critically reading the manuscript. We also gratefully acknowledge Richard Henderson, Judith Short and Juliet A. Ellis (King's College, London, UK) for helpful suggestions. VMK is supported by FEBS Long-term Fellowship; BZ is supported by EMBO Long-term Fellowship.
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