|Failure of amino acid homeostasis causes cell death following proteasome inhibition.|
|Jump to Full Text|
|PMID: 22959274 Owner: NLM Status: MEDLINE|
|The ubiquitin-proteasome system targets many cellular proteins for degradation and thereby controls most cellular processes. Although it is well established that proteasome inhibition is lethal, the underlying mechanism is unknown. Here, we show that proteasome inhibition results in a lethal amino acid shortage. In yeast, mammalian cells, and flies, the deleterious consequences of proteasome inhibition are rescued by amino acid supplementation. In all three systems, this rescuing effect occurs without noticeable changes in the levels of proteasome substrates. In mammalian cells, the amino acid scarcity resulting from proteasome inhibition is the signal that causes induction of both the integrated stress response and autophagy, in an unsuccessful attempt to replenish the pool of intracellular amino acids. These results reveal that cells can tolerate protein waste, but not the amino acid scarcity resulting from proteasome inhibition.|
|Amila Suraweera; Christian Münch; Ariane Hanssum; Anne Bertolotti|
Related Documents :
|10933134 - Structure-activity relationships of anthraquinones in the decrease of intestinal motility.
23116114 - Nucleic acids electro-transfer: from bench to bedside.
16658174 - Dark fixation of co(2) by crassulacean plants: evidence for a single carboxylation step.
22457144 - Current progress of research on pharmacologic actions of salvianolic acid b.
5324304 - Some factors affecting cyclopropane acid formation in escherichia coli.
2212394 - The comparative effects of n-3 and n-6 polyunsaturated fatty acids on plasma fibrinogen...
|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-09-06|
|Title: Molecular cell Volume: 48 ISSN: 1097-4164 ISO Abbreviation: Mol. Cell Publication Date: 2012 Oct|
|Created Date: 2012-10-29 Completed Date: 2013-04-03 Revised Date: 2014-02-20|
Medline Journal Info:
|Nlm Unique ID: 9802571 Medline TA: Mol Cell Country: United States|
|Languages: eng Pagination: 242-53 Citation Subset: IM|
|Copyright © 2012 Elsevier Inc. All rights reserved.|
|APA/MLA Format Download EndNote Download BibTex|
Cell Death / physiology
Drosophila melanogaster / metabolism
NIH 3T3 Cells
Proteasome Endopeptidase Complex* / metabolism, physiology
Saccharomyces cerevisiae / metabolism
Ubiquitin / metabolism
|MC_U105185860//Medical Research Council; //Medical Research Council|
|0/Amino Acids; 0/Ubiquitin; EC 188.8.131.52/Proteasome Endopeptidase Complex|
Journal ID (nlm-ta): Mol Cell
Journal ID (iso-abbrev): Mol. Cell
Publisher: Cell Press
© 2012 ELL & Excerpta Medica.
Received Day: 2 Month: 2 Year: 2012
Revision Received Day: 4 Month: 6 Year: 2012
Accepted Day: 3 Month: 8 Year: 2012
pmc-release publication date: Day: 26 Month: 10 Year: 2012
Print publication date: Day: 26 Month: 10 Year: 2012
Volume: 48 Issue: 2
First Page: 242 Last Page: 253
PubMed Id: 22959274
Publisher Id: MOLCEL4405
|Failure of Amino Acid Homeostasis Causes Cell Death following Proteasome Inhibition|
|Anne Bertolotti1∗||Email: firstname.lastname@example.org|
1MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK
2Department of Cell Biology, Harvard Medical School, Boston, MA 02115, USA
|∗Corresponding author email@example.com
The controlled degradation of proteins by the proteasome is essential in all cells and impairment of the ubiquitin-proteasome system contributes to many pathological conditions (Hershko and Ciechanover, 1998; Finley, 2009). Although the proteasome inhibitor Bortezomib is used for the treatment of multiple myeloma (Hideshima et al., 2001; Goldberg, 2007; Navon and Ciechanover, 2009), it remains unclear how proteasome failure kills cells.
Because the ubiquitin-proteasome system controls the degradation of a large number of cellular proteins including short-lived, regulatory, and damaged or misfolded proteins (Hershko and Ciechanover, 1998; Schwartz and Ciechanover, 2009), it has been assumed that accumulation of no-longer needed proteins underlies the toxicity of proteasome inhibition. However, how such proteins become harmful to cells and organisms remains unclear. Failure to degrade key regulatory proteins could also perturb cellular function. The transcription regulator NF-κB is one such regulatory protein activated by proteasome cleavage (Palombella et al., 1994). NF-κB is constitutively activated in multiple myeloma and thus was thought to be a prominent target of proteasome inhibitors (Schwartz and Ciechanover, 2009). However, as selective inhibition of NF-κB does not recapitulate the cytotoxic effects of proteasome inhibition (Hideshima et al., 2002), alternative mechanisms need to be considered.
The function of the proteasome in protein waste disposal has been extensively studied (Hershko and Ciechanover, 1998; Finley, 2009). In addition to this well-described function, the proteasome also recycles amino acids. The importance of this aspect of proteasomal degradation for normal cell and organismal function is unclear. In contrast, recycling amino acids is a well-established function of autophagy in starving cells (Nakatogawa et al., 2009). Under conditions of amino acid starvation, both autophagy and proteasomal degradation are required to maintain adequate amino acid levels for sustaining protein synthesis (Onodera and Ohsumi, 2005; Vabulas and Hartl, 2005). Despite the established importance of protein recycling under conditions of severe nutrient deficiency, it is unclear whether protein degradation contributes an important fraction of the supply of amino acids under physiological conditions.
Because the mechanisms underlying the toxicity resulting from proteasome inhibition are unclear, and as it is unknown whether protein degradation contributes an essential fraction of the intracellular amino acid pool under normal conditions, we examined whether the lethality resulting from proteasome inhibition is mediated by perturbation of amino acid homeostasis. In three model systems—yeast, mammalian cells, and Drosophila—we find that proteasome inhibition causes a lethal shortage of amino acids and the lethality resulting from proteasome inhibition is rescued upon amino acid supplementation, without any detectable decrease in the levels of proteasome substrates in proteasome-inhibited cells.
We first assessed whether amino acid homeostasis was altered following proteasome impairment in yeast. As expected (Ghislain et al., 1993), exposure to 37°C for 20 hr was lethal to the yeast proteasome mutant cim3-1, harboring a thermosensitive mutation in the regulatory subunit Rpt6 (Figure S1A available online). We next monitored the levels of free amino acids in yeast cells following proteasome inhibition. Exponentially growing yeast cells were inoculated at an optical density of 0.2 and grown at 30°C in the standard rich medium yeast peptone dextrose (YPD) to insure that the yeast cells were replete with nutrients. Five hours after the switch to 37°C, the levels of most amino acids increased in wild-type cells (Figure 1A). This is likely the result of the heat shock, which is known to attenuate protein synthesis (Richter et al., 2010). Surprisingly, however, the levels of most free amino acids decreased in cim3-1 cells after 5 hr at 37°C (Figure 1A). Unlike wild-type cells, cim3-1 cells did not grow at 37°C (Figure S1B), indicating that the decrease in intracellular amino acids in cim3-1 cells was not due to an exhaustion of the nutrient supply from the media as a result of cell growth. Thus, inhibition of proteasomal degradation, under conditions of nutrient sufficiency, decreases the levels of intracellular amino acid in yeast cells.
We then investigated whether increasing the supply of amino acids could rescue cim3-1 cells. Exponentially growing wild-type or cim3-1 yeast cells were inoculated at an optical density of 0.2 and cultured in the standard rich medium YPD for 21 hr, labeled with propidium iodide to reveal dead cells, and analyzed by flow cytometry. Unlike wild-type cells, the vast majority of cim3-1 cells died after 21 hr of culture at 37°C in rich media (Figure 1B). supplementation with amino acids prevented the death of the cim3-1 cells exposed to 37°C (Figure 1B). To determine whether such cells were viable, they were spotted on rich plates and grown at the permissive temperature. Unlike the nonsupplemented cim3-1 cells, cim3-1 cells that had been exposed to 37°C in the presence of additional amino acids were viable and gave rise to the same number of colonies as wild-type cells at 30°C (Figure 1C). This revealed that amino acid supplementation prevents death of proteasome-inhibited yeast cells. This rescuing effect occurs without promoting cell growth because the number of viable cells exposed to 37°C in the presence of amino acids equaled the number of cells prior exposure to 37°C (Figure 1C, compare lane 1 to lane 3). Supplementation with amino acids also protected cim3-1 cells exposed to 37°C on plates (Figure 1D), as well as the proteasome mutant pre1-1 cells, harboring a thermosensitive mutation in the β4 subunit of the 20S proteasome (Heinemeyer et al., 1991) (Figure 1E), but not the ndc80-1 mutant cells (Figure S1C), which harbors a thermosensitive mutation unrelated to the proteasome, in a spindle body component (Wigge et al., 1998).
Although rescuing viability, addition of amino acids did not noticeably decrease the levels of polyubiquitinated proteins (Figure 1F) or the unstable GFP-tagged Ura3-3 (Lewis and Pelham, 2009) that accumulated in cim3-1 cells at 37°C (Figure 1G). Thus, amino acid supplementation rescues from the lethality resulting from proteasome inhibition without promoting a recovery of proteasome function.
Proteasomal degradation is required for progression through the cell cycle (Hershko, 2005) and at nonpermissive temperature, cim3-1 cells stop dividing (Ghislain et al., 1993) and (Figure S1B) and accumulate cyclins, such as CLB2 (Ghislain et al., 1993). Although rescuing the viability of proteasome-inhibited cells, amino acids supplementation did not alleviate the growth arrest resulting from proteasome inhibition (Figure S1B). Consistently, the levels of CLB2 were indistinguishable in cim3-1 cells at 37°C with or without amino acids supplementation (Figure 1H). This confirmed that amino acids did not rescue proteasomal degradation or the resulting growth impairment in proteasome inhibited cells, while rescuing viability.
We next examined if the marked decrease in amino acid noted in cim3-1 cells impacted on protein synthesis. Note that, as expected (Richter et al., 2010), heat shock reduced protein synthesis in wild-type cells (Figure 1I). Strikingly, we found that in cim3-1 cells, protein synthesis at 37°C was reduced to 19% of the wild-type cells exposed to the same temperature (Figure 1I). Supplementation with amino acids rescued translation rates in the cim3-1 cells to nearly wild-type levels (Figure 1I).
Because proteasome function is conserved in evolution, we next examined whether inhibition of the proteasome altered amino acid homeostasis in mammalian cells. Treatment of mammalian NIH 3T3 cells with the proteasome inhibitors MG-132 or Bortezomib decreased the levels of the amino acids asparagine/aspartate and cysteine, whereas the levels of other amino acids remained largely unchanged or only marginally increased (Figure S2A). To address whether the decrease in cysteine and asparagine/aspartate were detrimental to cells following proteasome inhibition, we examined whether supplementation with these amino acids affected cell viability of proteasome-inhibited cells. Amino acids were added after a transient treatment with the proteasome inhibitor to ensure that the amino acids did not interfere with the proteasome inhibitors. Addition of cysteine following treatment with MG-132 for 8 hr dramatically increased cell survival and markedly reduced apoptosis in a dose-dependent manner, in contrast to other amino acids, the reducing agent β-mercaptoethanol, or the antioxidant ascorbic acid (Figures S2B and S2C). Cysteine also markedly increased cell viability following Bortezomib treatment (Figure S2D). Asparagine further increased viability, when added together with cysteine following an 8 hr MG-132 treatment, whereas it only had a minor effect on its own (Figure 2A). It may not be a coincidence that both cysteine and asparagine are conditionally essential amino acids (Reeds, 2000), absent in the Dulbecco’s modified Eagle’s medium (DMEM). Although rescuing the viability of proteasome-inhibited cells, amino acid supplementation had no significant effect on the proliferation of untreated cells (Figure S2E) and neither cysteine nor asparagine detectably altered proteasome activity (Figure S2F). Thus, supplementation with the critical amino acids depleted upon proteasome inhibition rescued survival of ∼90% of proteasome-impaired cells, without rescuing proteasome activity.
To dissect the mechanism underlying the rescued viability of proteasome-inhibited cells by amino acid supplementation, we next focused on cysteine addition as it had a potent effect. We monitored the abundance of polyubiquitinated proteins as well as the proteasome reporter substrates UbG76V-GFP, ZsGreen-ODC, and GFP-CL1 (Dantuma et al., 2000; Hoyt et al., 2005; Gilon et al., 1998; Bence et al., 2001). Although markedly increasing the survival of three different cell lines following proteasome inhibition (Figure S2G), addition of cysteine did not reduce the abundance of either polyubiquitinated proteins (Figure 2B) or the three different rapidly degraded, proteasome reporter-substrates UbG76V-GFP, ZsGreen-ODC, and GFP-CL1 (Figure 2C). Similarly, cells accumulated indistinguishable levels of the proteasome reporter substrate ZsGreen-ODC when treated with MG-132 alone or together with 1 mM cysteine (Figure 2D). Addition of cysteine together with MG-132 also rescued the viability of proteasome-inhibited cells (Figure S2G). These results demonstrate that cysteine did not antagonize MG-132, while rescuing viability of cells following proteasome inhibition.
The proteasome activates the transcription regulator NF-κB by proteolytic cleavage of the precursor p105 into p50 (Palombella et al., 1994). Although rescuing cell viability (Figure 2A), cysteine supplementation did not reduce the impairment of the proteasome-mediated processing of the transcription regulator NF-κB, p105 into p50, in cells treated with MG-132 for 8 hr (Figure 2E). These results reveal that while rescuing from the lethality resulting from proteasome inhibition, supplementation with an amino acid selectively depleted following proteasome inhibition did not decrease the levels of polyubiquitinated proteins, proteasome reporter substrates and the impairment of NF-kB processing in proteasome-inhibited cells. Thus, cells can tolerate proteasome inhibition but not the resulting amino acid insufficiency.
Proteasome inhibition, like many different stresses, induces the integrated stress response (ISR) (Jiang and Wek, 2005). However, the signal responsible for the ISR induction in proteasome-inhibited cells is unknown. The ISR is an adaptive response to many forms of stresses, which converge into phosphorylating the α subunit of translation initiation factor 2 (eIF2α) thereby reprogramming protein synthesis. When eIF2α is phosphorylated, general protein synthesis is attenuated, whereas ATF4 is selectively translated (Harding et al., 2003). ATF4 is a transcription factor, which controls expression of genes involved in amino acid import and biosynthesis (Harding et al., 2003), as well as the transcription factor CHOP, which in turn induces GADD34 (Figure 3A). GADD34 is a regulatory subunit of the serine/threonine phosphatase PP1, which recruits PP1 in stressed cells to dephosphorylate eIF2α and terminates stress signaling (Novoa et al., 2003). Having found that proteasome inhibition caused a lethal shortage in both cysteine and asparagine, and because genes involved in the biosynthesis of cysteine and asparagine are prominent targets of the ISR (Harding et al., 2003), we examined whether amino acid scarcity may be the signal that induces the ISR in proteasome inhibited cells (Figure 3A). If so, amino acid supplementation should attenuate ISR signaling in response to proteasome inhibition. In the absence of MG-132, the ISR was not induced, confirming that untreated cells were not stressed (Figure 3B). As expected (Jiang and Wek, 2005), MG-132 induced the ISR, and this is manifested by the phosphorylation of eIF2α, expression of ATF4 and the pro-death proteins CHOP and GADD34 (Figure 3B). Strikingly, the levels of CHOP and GADD34 remained elevated in the MG-132 cells 6 hr after the removal of the proteasome inhibitor, in agreement with the finding that such cells were committed to die (Figure 2A). In contrast, in cells supplemented with cysteine, a marked decrease in the levels of CHOP and GADD34 was detected 4–6 hr following the cysteine washout (Figure 3B), in good agreement with the cytoprotective effect of cysteine upon proteasome inhibition (Figure 2A). When added together with MG-132, cysteine virtually abrogated the induction of the ISR resulting from proteasome inhibition, without altering the levels of polyubiquitinated proteins (Figure S3). This reveals that the amino acid shortage resulting from proteasome inhibition is the signal that induces the ISR in proteasome-inhibited cells.
To confirm that CHOP-mediated cell death following proteasome inhibition (Jiang and Wek, 2005), we monitored the survival of wild-type and CHOP−/− cells (Marciniak et al., 2004) following proteasome inhibition. Genetic ablation of CHOP markedly enhanced survival of proteasome-inhibited cells (Figure 3C). The decreased CHOP levels in NIH 3T3 cells supplemented with cysteine following proteasome inhibition could be due to an enhanced degradation or a decreased synthesis. We found that addition of cysteine did not rescue proteasomal degradation (Figures 2B–2E) and the stability of both GADD34 and CHOP were indistinguishable in cells that had been supplemented or not with cysteine, following proteasome inhibition (Figure 3D). Thus, the low levels of CHOP in proteasome-inhibited cells supplemented with cysteine did not reflect an increased degradation but rather, a decreased synthesis of this stress protein, as a result of the dephosphorylation of eIF2α following cysteine supplementation (Figure 2B).
The marked attenuation of eIF2α phosphorylation by cysteine supplementation in proteasome-inhibited cells suggested that the supply of cysteine might be rate-limiting for global protein synthesis in proteasome-inhibited cells. If so, cysteine supplementation may rescue global protein synthesis while attenuating translation of stressed proteins such as CHOP. We next tested this hypothesis. As expected (Jiang and Wek, 2005), proteasome inhibition caused a pronounced inhibition of protein synthesis (Figure 3E). Remarkably, addition of 1 mM cysteine largely prevented the translation attenuation resulting form proteasome inhibition (Figure 3E). GCN2 is the eIF2α kinase that mediates the ISR induction in response to amino acid deprivation (Harding et al., 2000; Zhang et al., 2002). Genetic ablation of GCN2 virtually abolished eIF2α phosphorylation upon proteasome inhibition (Figure 3F). Furthermore, activated and phosphorylated GCN2 was detected in cells deprived of leucine or MG-132-treated cells, and addition of cysteine markedly reduced GCN2 phosphorylation upon proteasome inhibition (Figure 3G). This establishes that inhibition of proteasomal degradation causes a shortage of critical amino acids that induce the ISR via GCN2.
To confirm that the attenuation of eIF2α phosphorylation by cysteine in proteasome inhibited cells is due to the replenishment of this otherwise limiting amino acid, as opposed to a suppression of ISR signaling by an indirect effect, we tested whether cysteine affected eIF2α phosphorylation induced by ultraviolet (UV) irradiation, a different stress than amino acid limitation (Deng et al., 2002). We found that the induction of eIF2α phosphorylation by UV was not reduced by supplementation with cysteine (Figure 3H). Thus, cysteine supplementation selectively alleviates eIF2α phosphorylation in proteasome-inhibited cells, but not in UV-irradiated cells.
Although polyubiquitination is the canonical signal to target proteins for proteasomal degradation, recent studies have revealed that polyubiquitinated proteins can also be degraded by autophagy (Kirkin et al., 2009). Autophagy is also induced when proteasomal degradation is inhibited (Rideout et al., 2004; Iwata et al., 2005) and alleviates the toxicity resulting from proteasome inhibition (Korolchuk et al., 2010; Pandey et al., 2007). However, the mechanisms underlying autophagy induction when proteasomal degradation is compromised are unknown. As expected (Korolchuk et al., 2010), MG-132 increased the number of GFP-LC3 labeled autophagosomes in HeLa cells stably expressing GFP-LC3 (Figures 4A and 4B). Strikingly, cysteine supplementation markedly decreased the number of fluorescent puncta in proteasome-inhibited cells (Figures 4A and 4B). In contrast, supplementation with other amino acids, reducing agents or antioxidants did not noticeably reduced the number of GFP-LC3 puncta in proteasome inhibited cells (Figure S4). Cysteine is not a generic suppressor of autophagosome accumulation because cysteine did not decrease the number of GFP-LC3 puncta that accumulated in cells treated with Bafilomycin A1 (Figures 4A and 4B), an inhibitor of autophagosome-lysosome fusion (Mizushima et al., 2010). MG-132 treatment also increased the levels of LC3-II (Figures 4C and 4D) but this was markedly decreased in the presence of cysteine (Figures 4C and 4D). These results establish that the decrease in a critical amino acid is the signal that induces autophagy when proteasomal degradation is inhibited. To assess whether induction of autophagy contributed to protect cells from proteasome-inhibition, we compared the survival of wild-type or Atg5−/− cells (Kuma et al., 2004) following proteasome inhibition. We found that Atg5−/− cells were significantly more sensitive to MG-132 treatment and this was manifest already following 1 hr of proteasome inhibition (Figure 4E).
The mammalian target of rapamycin (mTOR) signaling pathway senses and responds to amino acid availability to modulate protein synthesis via the phosphorylation of substrates such as S6 kinase 1 (S6K1) (Ma and Blenis, 2009) (Figure 5A). To evaluate whether autophagy contributed to replenish the pool of intracellular amino acids upon proteasome inhibition, we measured the levels of phosphorylation of threonine 389 of the mTORC1 substrate S6K1 (Ma and Blenis, 2009). In agreement with the decrease in critical amino acids following proteasome inhibition, S6K1 phosphorylation decreased 1 hr after MG-132 addition (Figure 5B). Four hours following MG-132 addition, S6K1 phosphorylation increased (Figure 5B). This increase was abrogated by Bafilomycin A1, indicating that it was dependent on autophagic degradation (Figure 5B). Amino acid sensing by mTOR is mediated by the Rag GTPases and dominant negative mutants of the Rag GTPases abrogate mTOR stimulation by amino acids (Sancak et al., 2008). Strikingly, overexpression of dominant negative mutants of the Rag GTPases that prevent amino acid sensing by mTORC1 (Figure 5A) also abolished the increased phosphorylation of S6K1 that followed proteasome inhibition (Figure 5C). These results reveal that amino acid scarcity is the signal that induces autophagy when the proteasome is inhibited, in an attempt to rescue amino acid homeostasis.
This model predicts that blocking amino acid consumption by inhibiting protein synthesis should recapitulate the rescuing effects of amino acid supplementation in proteasome inhibited cells. Indeed, we found that addition of cycloheximide together with MG-132 prevented the decreased S6K1 phosphorylation resulting from treatment with MG-132 for 1 hr (Figure 5D). Consistently, the decrease in cysteine and asparagine/aspartate resulting from proteasome inhibition was markedly attenuated in cells cotreated with cycloheximide (Figure 5E). Strikingly, cycloheximide protected cells from the lethality resulting from proteasome inhibition (Figure 5F). The rescuing effect of cycloheximide in proteasome-inhibited cells was selective because cycloheximide increased the lethality of cells exposed to UV irradiation (data not shown). Thus, inhibition of protein synthesis markedly attenuates the depletion of critical amino acid following proteasome inhibition as well as the lethality resulting from proteasome inhibition.
We next assessed whether proteasome inhibition had detrimental consequences on amino acid homeostasis in an organismal context. We exposed Drosophila to proteasome inhibitors and monitored amino acid levels. Bortezomib significantly reduced the levels of asparagine/aspartate, threonine/serine, glutamine/glutamate, phenylalanine, and proline in Drosophila (Figure 6A). Bortezomib also increased the levels of glycine (Figure 6A), similar to prolonged starvation in humans (Felig et al., 1969). As expected (Vernace et al., 2007), exposure of flies to Bortezomib was lethal (Figure 6B). Amino acid supplementation markedly increased survival of proteasome-inhibited flies (Figure 6B), without detectable changes in the levels of proteasome substrates (Figure 6C). Thus, proteasome inhibition caused an intolerable amino acid imbalance in flies and the resulting lethality was rescued upon supplementation with amino acids.
Here, we show that the detrimental consequences of proteasome inhibition are largely abrogated by supplementation with amino acids in yeast, mammalian cells, and Drosophila (Figure 7). Strikingly, the rescuing effect of amino acids occurs without reducing the accumulation of proteasome substrates. These findings reveal that cells can survive with the protein waste they accumulate when the proteasome is inhibited but the resulting amino acid deficiency is lethal. Thus, the proteasome substrates accumulating upon proteasome inhibition appear detrimental to cells as they sequester a pool of critical amino acids that would otherwise be recycled.
Although abrogating death of proteasome-inhibited cells, amino acid supplementation does not abrogate the requirement for proteasomal degradation for regulatory functions such as cell division. The amino acid scarcity resulting from proteasome inhibition induces the classical set of responses to amino acid starvation, in an vain attempt to sustain amino acid homeostasis. Although it had been previously reported that proteasome inhibition, like many different stresses, induces eIF2α phosphorylation and that the resulting translation attenuation is abrogated by genetic impairment of eIF2α phosphorylation (Jiang and Wek, 2005), the underlying mechanism was unknown. We have shown here that the amino acid decrease following proteasome inhibition is the signal that activates GCN2 and induces eIF2α phosphorylation, leading to attenuation of protein synthesis (Figure 3). Cysteine is the least abundant cellular amino acid and we found that cysteine scarcity following proteasome inhibition impairs protein synthesis. Upon persistent inhibition of the proteasome and the subsequent amino acid insufficiency, the ISR is chronically activated, thereby leading to the expression of the pro-apoptotic protein CHOP (Figure 3B). Supplementation with a critical amino acid, depleted upon proteasome inhibition, virtually suppresses ISR signaling and cell death (Figure 3B), similar to genetic ablation of CHOP (Figure 3C) or impairment of eIF2α phosphorylation, which reduces death following proteasome inhibition (Jiang and Wek, 2005).
The mechanisms underlying the crosstalk between autophagic and proteasomal degradation have remained elusive. In this study, we provide the missing link between autophagy induction and proteasome inhibition. We show that the signal responsible for autophagy induction upon proteasome inhibition is the resulting amino acid scarcity, the canonical inducer of autophagy. Autophagy aims at protecting cells from the deleterious consequences of proteasome inhibition, as cells lacking Atg5, a key autophagy component are more sensitive to proteasome inhibition. Both the ISR and autophagy are involved as early as 1 hr following proteasome inhibition to adapt cells to the resulting changes. Our work shows that autophagy and proteasomal degradation act in a concerted manner to adjust the supply of amino acids to the cellular needs. Following proteasome inhibition, autophagy attempts to restore amino acid homeostasis, as manifested by an increased S6K1 phosphorylation via the canonical, Rag GTPases-dependent amino acid signaling pathway to mTOR. The findings reported here reveal how changes in amino acid homeostasis are integrated with protein metabolism and cell death (Figure 7).
We found here that the deleterious consequences of proteasome inhibition are rescued upon amino acid supplementation in yeast, mammalian cells, and Drosophila. These findings establish the importance of proteasomal degradation in recycling amino acids for normal cell and organismal function. There is a qualitative difference in the required amino acids in the three different systems that is not surprising as yeast, mammalian cells, and Drosophila have different properties and requirements. Yeast cells required a broad range of amino acids to survive proteasome inhibition, perhaps because they have higher metabolic needs, as they divide more rapidly than mammalian cells. Upon proteasome inhibition, mammalian cells had a prominent need for cysteine and asparagine and we show that the decrease in cysteine and asparagine/aspartate were largely prevented by blocking protein synthesis in proteasome-inhibited cells (Figure 5E). Notably, enzymes required for the metabolism of cysteine and asparagine, two conditionally essential amino acids, are under the control of the ISR, thus underscoring an evolutionary pressure to maintain the levels of asparagine and cysteine in the cell. In addition, the importance of asparagine starvation has been previously recognized and is the basis for the use of L-asparaginase for the treatment of acute lymphoblastic leukemia (Müller and Boos, 1998).
The proteasome inhibitor Bortezomib is used in cancer therapy but it is limited to the treatment of multiple myeloma and restricted by adverse effects, such as peripheral neuropathy (Richardson et al., 2003). So far, the mechanisms by which proteasome inhibitors kill cells have remained elusive. Failure of amino acid homeostasis not only explains the lethality resulting from proteasome inhibition but also provides a foundation for the development of novel cancer therapies.
NIH 3T3, 293T (ATCC), 293T cells stably expressing ZsGreen-ODC (ZsProsensor-1 cells, Clontech), and HeLa cells were maintained at 37°C in DMEM supplemented with 10% fetal bovine serum (FBS), penicillin, and streptomycin. MEFs cells were cultured in DMEM supplemented with penicillin, streptomycin, glutamine, 1× nonessential amino acids (Sigma), sodium pyruvate, and 10% FBS.
Cells were plated (day 0) in DMEM supplemented with 10% FBS bovine serum in 24-well plates (Nunc), at a density of 8,000 cells/ml. The next day (day 1), media were replaced with DMEM supplemented with 0.5% FBS. On day 2, cells were treated with proteasome inhibitors for the indicated period of time. Media containing proteasome inhibitors were replaced with DMEM supplemented with 0.5% FBS and the indicated additives. Four wells per condition were used. On day 3, media were replaced with DMEM supplemented with 10% FBS. Cells were kept for 2–3 days as indicated. Cell viability was assessed by measuring the reduction of WST-8 [2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfophenyl)-2H-tetrazolium] into formazan using Cell Viability Counting Kit-8 (Dojindo) according to the supplier’s recommendation.
Flow cytometry analyses were performed on a FACSCalibur flow cytometer (BD Biosciences) and analyzed with FlowJo and confocal microscopy was carried out as described in Münch et al. (2011).
Cell lysis, immunoblots, and measurement of translation rates were performed as described in Tsaytler et al. (2011). Note that cells were not starved in methionine-free media before labeling with 35S-methionine for monitoring protein synthesis.
Cim3-1 or pre1-1 and their respective isogenic wild-type strains (Ghislain et al., 1993; Heinemeyer et al., 1991) and ndc80-1 (Wigge et al., 1998) were grown in YPD medium using standard techniques, as in Dehay and Bertolotti (2006).
Wild-type Oregon R flies were reared on standard food. Amino acids were extracted in 600 μl methanol from 5 frozen female flies per condition, as in Hayward et al. (1993). The suspension was centrifuged and the supernatant collected, vacuum-dried, and analyzed. Some amino acids were below detection levels in such analyses. For survival experiments, 20 flies, both females and males, were kept in vials lined with 3 mm filter paper and fed a solution of 5% sucrose with either vehicle (0.5% DMSO, control) or with Bortezomib (50 μM in DMSO), for the indicated time, as in Vernace et al. (2007). Under the same conditions MG-132 (50 μM in DMSO) was not toxic. In Figure 6B, 1.5 ml of 5% sucrose with or without amino acids at the concentration used in Grandison et al. (2009) was added together with the proteasome inhibitor. Proteins were extracted from five frozen female flies per conditions in 250 μl boiling Laemmli buffer supplemented with 10 mM NEM and 50 mM DTT.
Data are presented as means and SD or SEM, as indicated. Where indicated, two groups were compared with a two-tailed nonpaired Student’s t test.
|Bence N.F.,Sampat R.M.,Kopito R.R.. Impairment of the ubiquitin-proteasome system by protein aggregationScience292Year: 20011552155511375494|
|Dantuma N.P.,Lindsten K.,Glas R.,Jellne M.,Masucci M.G.. Short-lived green fluorescent proteins for quantifying ubiquitin/proteasome-dependent proteolysis in living cellsNat. Biotechnol.18Year: 200053854310802622|
|Dehay B.,Bertolotti A.. Critical role of the proline-rich region in Huntingtin for aggregation and cytotoxicity in yeastJ. Biol. Chem.281Year: 2006356083561516973603|
|Deng J.,Harding H.P.,Raught B.,Gingras A.C.,Berlanga J.J.,Scheuner D.,Kaufman R.J.,Ron D.,Sonenberg N.. Activation of GCN2 in UV-irradiated cells inhibits translationCurr. Biol.12Year: 20021279128612176355|
|Felig P.,Owen O.E.,Wahren J.,Cahill G.F.J. Jr.. Amino acid metabolism during prolonged starvationJ. Clin. Invest.48Year: 19695845945773094|
|Finley D.. Recognition and processing of ubiquitin-protein conjugates by the proteasomeAnnu. Rev. Biochem.78Year: 200947751319489727|
|Ghislain M.,Udvardy A.,Mann C.. S. cerevisiae 26S protease mutants arrest cell division in G2/metaphaseNature366Year: 19933583628247132|
|Gilon T.,Chomsky O.,Kulka R.G.. Degradation signals for ubiquitin system proteolysis in Saccharomyces cerevisiaeEMBO J.17Year: 1998275927669582269|
|Goldberg A.L.. Functions of the proteasome: from protein degradation and immune surveillance to cancer therapyBiochem. Soc. Trans.35Year: 2007121717212580|
|Grandison R.C.,Piper M.D.,Partridge L.. Amino-acid imbalance explains extension of lifespan by dietary restriction in DrosophilaNature462Year: 20091061106419956092|
|Harding H.P.,Novoa I.,Zhang Y.,Zeng H.,Wek R.,Schapira M.,Ron D.. Regulated translation initiation controls stress-induced gene expression in mammalian cellsMol. Cell6Year: 20001099110811106749|
|Harding H.P.,Zhang Y.,Zeng H.,Novoa I.,Lu P.D.,Calfon M.,Sadri N.,Yun C.,Popko B.,Paules R.. An integrated stress response regulates amino acid metabolism and resistance to oxidative stressMol. Cell11Year: 200361963312667446|
|Hayward D.C.,Delaney S.J.,Campbell H.D.,Ghysen A.,Benzer S.,Kasprzak A.B.,Cotsell J.N.,Young I.G.,Miklos G.L.. The sluggish-A gene of Drosophila melanogaster is expressed in the nervous system and encodes proline oxidase, a mitochondrial enzyme involved in glutamate biosynthesisProc. Natl. Acad. Sci. USA90Year: 1993297929838096642|
|Heinemeyer W.,Kleinschmidt J.A.,Saidowsky J.,Escher C.,Wolf D.H.. Proteinase yscE, the yeast proteasome/multicatalytic-multifunctional proteinase: mutants unravel its function in stress induced proteolysis and uncover its necessity for cell survivalEMBO J.10Year: 19915555622001673|
|Hershko A.. The ubiquitin system for protein degradation and some of its roles in the control of the cell division cycleCell Death Differ.12Year: 20051191119716094395|
|Hershko A.,Ciechanover A.. The ubiquitin systemAnnu. Rev. Biochem.67Year: 19984254799759494|
|Hideshima T.,Richardson P.,Chauhan D.,Palombella V.J.,Elliott P.J.,Adams J.,Anderson K.C.. The proteasome inhibitor PS-341 inhibits growth, induces apoptosis, and overcomes drug resistance in human multiple myeloma cellsCancer Res.61Year: 20013071307611306489|
|Hideshima T.,Chauhan D.,Richardson P.,Mitsiades C.,Mitsiades N.,Hayashi T.,Munshi N.,Dang L.,Castro A.,Palombella V.. NF-kappa B as a therapeutic target in multiple myelomaJ. Biol. Chem.277Year: 2002166391664711872748|
|Hoyt M.A.,Zhang M.,Coffino P.. Probing the ubiquitin/proteasome system with ornithine decarboxylase, a ubiquitin-independent substrateMethods Enzymol.398Year: 200539941316275346|
|Iwata A.,Riley B.E.,Johnston J.A.,Kopito R.R.. HDAC6 and microtubules are required for autophagic degradation of aggregated huntingtinJ. Biol. Chem.280Year: 2005402824029216192271|
|Jiang H.Y.,Wek R.C.. Phosphorylation of the alpha-subunit of the eukaryotic initiation factor-2 (eIF2alpha) reduces protein synthesis and enhances apoptosis in response to proteasome inhibitionJ. Biol. Chem.280Year: 2005141891420215684420|
|Kirkin V.,McEwan D.G.,Novak I.,Dikic I.. A role for ubiquitin in selective autophagyMol. Cell34Year: 200925926919450525|
|Korolchuk V.I.,Menzies F.M.,Rubinsztein D.C.. Mechanisms of cross-talk between the ubiquitin-proteasome and autophagy-lysosome systemsFEBS Lett.584Year: 20101393139820040365|
|Kuma A.,Hatano M.,Matsui M.,Yamamoto A.,Nakaya H.,Yoshimori T.,Ohsumi Y.,Tokuhisa T.,Mizushima N.. The role of autophagy during the early neonatal starvation periodNature432Year: 20041032103615525940|
|Lewis M.J.,Pelham H.R.. Inefficient quality control of thermosensitive proteins on the plasma membranePLoS ONE4Year: 2009e503819337370|
|Ma X.M.,Blenis J.. Molecular mechanisms of mTOR-mediated translational controlNat. Rev. Mol. Cell Biol.10Year: 200930731819339977|
|Marciniak S.J.,Yun C.Y.,Oyadomari S.,Novoa I.,Zhang Y.,Jungreis R.,Nagata K.,Harding H.P.,Ron D.. CHOP induces death by promoting protein synthesis and oxidation in the stressed endoplasmic reticulumGenes Dev.18Year: 20043066307715601821|
|Mizushima N.,Yoshimori T.,Levine B.. Methods in mammalian autophagy researchCell140Year: 201031332620144757|
|Müller H.J.,Boos J.. Use of L-asparaginase in childhood ALLCrit. Rev. Oncol. Hematol.28Year: 1998971139768345|
|Münch C.,O’Brien J.,Bertolotti A.. Prion-like propagation of mutant superoxide dismutase-1 misfolding in neuronal cellsProc. Natl. Acad. Sci. USA108Year: 20113548355321321227|
|Nakatogawa H.,Suzuki K.,Kamada Y.,Ohsumi Y.. Dynamics and diversity in autophagy mechanisms: lessons from yeastNat. Rev. Mol. Cell Biol.10Year: 200945846719491929|
|Navon A.,Ciechanover A.. The 26 S proteasome: from basic mechanisms to drug targetingJ. Biol. Chem.284Year: 2009337133371819812037|
|Novoa I.,Zhang Y.,Zeng H.,Jungreis R.,Harding H.P.,Ron D.. Stress-induced gene expression requires programmed recovery from translational repressionEMBO J.22Year: 20031180118712606582|
|Onodera J.,Ohsumi Y.. Autophagy is required for maintenance of amino acid levels and protein synthesis under nitrogen starvationJ. Biol. Chem.280Year: 2005315823158616027116|
|Palombella V.J.,Rando O.J.,Goldberg A.L.,Maniatis T.. The ubiquitin-proteasome pathway is required for processing the NF-kappa B1 precursor protein and the activation of NF-kappa BCell78Year: 19947737858087845|
|Pandey U.B.,Nie Z.,Batlevi Y.,McCray B.A.,Ritson G.P.,Nedelsky N.B.,Schwartz S.L.,DiProspero N.A.,Knight M.A.,Schuldiner O.. HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPSNature447Year: 200785986317568747|
|Reeds P.J.. Dispensable and indispensable amino acids for humansJ. Nutr.130Year: 20001835S1840S10867060|
|Richardson P.G.,Barlogie B.,Berenson J.,Singhal S.,Jagannath S.,Irwin D.,Rajkumar S.V.,Srkalovic G.,Alsina M.,Alexanian R.. A phase 2 study of bortezomib in relapsed, refractory myelomaN. Engl. J. Med.348Year: 20032609261712826635|
|Richter K.,Haslbeck M.,Buchner J.. The heat shock response: life on the verge of deathMol. Cell40Year: 201025326620965420|
|Rideout H.J.,Lang-Rollin I.,Stefanis L.. Involvement of macroautophagy in the dissolution of neuronal inclusionsInt. J. Biochem. Cell Biol.36Year: 20042551256215325592|
|Sancak Y.,Peterson T.R.,Shaul Y.D.,Lindquist R.A.,Thoreen C.C.,Bar-Peled L.,Sabatini D.M.. The Rag GTPases bind raptor and mediate amino acid signaling to mTORC1Science320Year: 20081496150118497260|
|Schwartz A.L.,Ciechanover A.. Targeting proteins for destruction by the ubiquitin system: implications for human pathobiologyAnnu. Rev. Pharmacol. Toxicol.49Year: 2009739618834306|
|Thurston T.L.,Ryzhakov G.,Bloor S.,von Muhlinen N.,Randow F.. The TBK1 adaptor and autophagy receptor NDP52 restricts the proliferation of ubiquitin-coated bacteriaNat. Immunol.10Year: 20091215122119820708|
|Tsaytler P.,Harding H.P.,Ron D.,Bertolotti A.. Selective inhibition of a regulatory subunit of protein phosphatase 1 restores proteostasisScience332Year: 2011919421385720|
|Vabulas R.M.,Hartl F.U.. Protein synthesis upon acute nutrient restriction relies on proteasome functionScience310Year: 20051960196316373576|
|Vernace V.A.,Arnaud L.,Schmidt-Glenewinkel T.,Figueiredo-Pereira M.E.. Aging perturbs 26S proteasome assembly in Drosophila melanogasterFASEB J.21Year: 20072672268217413001|
|Wigge P.A.,Jensen O.N.,Holmes S.,Souès S.,Mann M.,Kilmartin J.V.. Analysis of the Saccharomyces spindle pole by matrix-assisted laser desorption/ionization (MALDI) mass spectrometryJ. Cell Biol.141Year: 19989679779585415|
|Zhang P.,McGrath B.C.,Reinert J.,Olsen D.S.,Lei L.,Gill S.,Wek S.A.,Vattem K.M.,Wek R.C.,Kimball S.R.. The GCN2 eIF2alpha kinase is required for adaptation to amino acid deprivation in miceMol. Cell. Biol.22Year: 20026681668812215525|
Document S1. Figures S1–S4 and Supplemental Experimental Procedures
We are grateful to D. Owen for amino acid analysis; C. Mann, D.H. Wolf, J. Kilmartin, M. Lewis, N. Mizushima, B. McGrath, D. Cavener, H. Harding, D. Ron, W. Greene, M. Narita, and F. Randow for reagents; M. Freeman, S. Aldaz Casanova, and M. Zettl for help and advice on the work with Drosophila; Z. Zhong for help with the revision; G. Lingley and P. Margiotta for help with figures and illustrations; and M.M. Babu, M. Goedert, M.H. Hastings, D. Komander, and S. Munro for discussions. This work was supported by the UK Medical Research Council.
Previous Document: Long Noncoding RNAs with snoRNA Ends.
Next Document: LIN28 binds messenger RNAs at GGAGA motifs and regulates splicing factor abundance.