Autophagy in the Cellular Energetic Balance
Open accessAbstract
Autophagy mediates the degradation of cellular components in lysosomes, assuring removal of altered or dysfunctional proteins and organelles. Autophagy is not only activated in response to cellular damage; in fact, one of its strongest and better-characterized stimuli is starvation. Activation of autophagy when nutrients are scarce allows cells to reutilize their own constituents for energy. Besides protein breakdown, autophagy also contributes to the mobilization of diverse cellular energy stores. This recently discovered interplay between autophagy and lipid and carbohydrate metabolism reveals the existence of a dynamic feedback between autophagy and cellular energy balance.
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The BLESS trial has shown modification in the microbiota of non-cystic fibrosis bronchiectasis patients receiving erythromycin for 48 months.
“The BLESS trial (115) has shown modification in the microbiota of non-cystic fibrosis bronchectasis patients receiving erythromycin for 48 months.”
From ESPEN guideline on clinical nutrition in the intensive care unit. (2019) · cites this paper as [115]
The cited paper’s sections on autophagy and lipid metabolism and on metabolic dysfunction discuss cellular energy balance, not the BLESS trial. Searches for BLESS, bronchiectasis, erythromycin, and airway microbiota found no passage addressing the claimed treatment or duration. (LLM, conf=0.78)
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Cites
Sancak, Y., Bar-Peled, L., Zoncu, R., Markhard, A. L., Nada, S., & Sabatini, D. M. (2010) · Cell · doi:10.1016/j.cell.2010.02.024 · Cited by 2,464 · see citing works
Impairment of starvation-induced and constitutive autophagy in <i>Atg7</i> -deficient mice
Komatsu, M., Waguri, S., Ueno, T., Iwata, J., Murata, S., Tanida, I., Ezaki, J., Mizushima, N., Ohsumi, Y., Uchiyama, Y., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412022 · Cited by 2,331 · see citing works
Nutrient-dependent mTORC1 Association with the ULK1–Atg13–FIP200 Complex Required for Autophagy
Hosokawa, N., Hara, T., Kaizuka, T., Kishi, C., Takamura, A., Miura, Y., Iemura, S.-I., Natsume, T., Takehana, K., Yamada, N., et al. (2009) · Molecular Biology of the Cell · doi:10.1091/mbc.e08-12-1248 · Cited by 2,076 · see citing works
Rabinowitz, J. D., & White, E. (2010) · Science · doi:10.1126/science.1193497 · Cited by 1,982 · see citing works
DRAM, a p53-Induced Modulator of Autophagy, Is Critical for Apoptosis
Crighton, D., Wilkinson, S., O'Prey, J., Syed, N., Smith, P., Harrison, P. R., Gasco, M., Garrone, O., Crook, T., & Ryan, K. M. (2006) · Cell · doi:10.1016/j.cell.2006.05.034 · Cited by 1,380 · see citing works
Defective Hepatic Autophagy in Obesity Promotes ER Stress and Causes Insulin Resistance
Yang, L., Li, P., Fu, S., Calay, E. S., & Hotamisligil, G. S. (2010) · Cell Metabolism · doi:10.1016/j.cmet.2010.04.005 · Cited by 1,274 · see citing works
Regulation of autophagy by cytoplasmic p53
Tasdemir, E., Maiuri, M. C., Galluzzi, L., Vitale, I., Djavaheri-Mergny, M., D'Amelio, M., Criollo, A., Morselli, E., Zhu, C., Harper, F., et al. (2008) · Nature Cell Biology · doi:10.1038/ncb1730 · Cited by 1,132 · see citing works
Vousden, K. H., & Ryan, K. M. (2009) · Nature Reviews Cancer · doi:10.1038/nrc2715 · Cited by 959 · see citing works
The Association of AMPK with ULK1 Regulates Autophagy
Lee, J. W., Park, S., Takahashi, Y., & Wang, H.-G. (2010) · PLoS ONE · doi:10.1371/journal.pone.0015394 · Cited by 482 · see citing works
PARTICIPATION OF LYSOSOMES IN CELLULAR AUTOPHAGY INDUCED IN RAT LIVER BY GLUCAGON
Deter, R. L., Baudhuin, P., & de Duve, C. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.35.2.c11 · Cited by 357 · cited 3× · see citing works
“Studies in cultured cells have shown that the proteasome system contributes most of the amino acids to this pool in the first hours of starvation (Vabulas and Hartl, 2005), whereas macroautophagy starts right after and reaches a peak at about 6–8 hr into the starvation period (Deter et al., 1967).”
InfluentialControl of autophagy initiation by phosphoinositide 3‐phosphatase jumpy
Vergne, I., Roberts, E., Elmaoued, R. A., Tosch, V., Delgado, M. A., Proikas‐Cezanne, T., Laporte, J., & Deretic, V. (2009) · The EMBO Journal · doi:10.1038/emboj.2009.159 · Cited by 270 · see citing works
Flagged first, then by citations
Research works printed but not linked: 63
- Aguado C Sarkar S Korolchuk VI Criado O Vernia S Boya P Sanz P de Cordoba SR Knecht E Rubinsztein DC Laforin, the most common protein mutated in Lafora disease, regulates autophagy Hum Mol Genet 2010 19 2867 2876 20453062 PMC2893813
- Arias E Cuervo AM Chaperone-mediated autophagy in protein quality control Curr Opin Cell Biol, e-pub ahead of publication 2010 PMC3078170 21094035
- Boland B Kumar A Lee S Platt FM Wegiel J Yu WH Nixon RA Autophagy induction and autophagosome clearance in neurons: relationship to autophagic pathology in Alzheimer's disease J Neurosci 2008 28 6926 6937 18596167 PMC2676733
- Chan EY Longatti A McKnight NC Tooze SA Kinase-inactivated ULK proteins inhibit autophagy via their conserved C-terminal domains using an Atg13-independent mechanism Mol Cell Biol 2009 29 157 171 18936157 PMC2612494
- Criollo A Senovilla L Authier H Maiuri MC Morselli E Vitale I Kepp O Tasdemir E Galluzzi L Shen S The IKK complex contributes to the induction of autophagy EMBO J 2010 29 619 631 19959994 PMC2830700
- Cuervo AM Autophagy and aging: keeping that old broom working Trends Genet 2008 24 604 612 18992957 PMC2745226
- Cuervo AM The plasma membrane brings autophagosomes to life Nature Cell Biology 2010 12 735 737 20680002
- Cuervo AM Knecht E Terlecky SR Dice JF Activation of a selective pathway of lysosomal proteolysis in rat liver by prolonged starvation Am J Physiol 1995 269 C1200 C1208 7491910
- Ebato C Uchida T Arakawa M Komatsu M Ueno T Komiya K Azuma K Hirose T Tanaka K Kominami E Autophagy is important in islet homeostasis and compensatory increase of beta cell mass in response to high-fat diet Cell Metab 2008 8 325 332 18840363
- Egan DF Shackelford DB Mihaylova MM Gelino S Kohnz RA Mair W Vasquez DS Joshi A Gwinn DM Taylor R Phosphorylation of ULK1 (hATG1) by AMP-activated protein kinase connects energy sensing to mitophagy Science 2011 331 456 461 21205641 PMC3030664
- Finn PF Dice JF Ketone bodies stimulate chaperone-mediated autophagy J Biol Chem 2005 280 25864 25870 15883160
- Fujitani Y Kawamori R Watada H The role of autophagy in pancreatic beta-cell and diabetes Autophagy 2009 5 280 282 19158492
- Fukuda T Roberts A Plotz PH Raben N Acid alpha-glucosidase deficiency (Pompe disease) Curr Neurol Neurosci Rep 2007 7 71 77 17217857
- Grasso D Sacchetti ML Bruno L Lo Re A Iovanna JL Gonzalez CD Vaccaro MI Autophagy and VMP1 expression are early cellular events in experimental diabetes Pancreatology 2009 9 81 88 19077458
- Gwinn DM Shackelford DB Egan DF Mihaylova MM Mery A Vasquez DS Turk BE Shaw RJ AMPK phosphorylation of raptor mediates a metabolic checkpoint Molecular Cell 2008 30 214 226 18439900 PMC2674027
- Hara T Nakamura K Matsui M Yamamoto A Nakahara Y Suzuki-Migishima R Yokoyama M Mishima K Saito I Okano H Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice Nature 2006 441 885 889 16625204
- Hashimoto D Ohmuraya M Hirota M Yamamoto A Suyama K Ida S Okumura Y Takahashi E Kido H Araki K Involvement of autophagy in trypsinogen activation within the pancreatic acinar cells J Cell Biol 2008 181 1065 1072 18591426 PMC2442206
- Jung CH Jun CB Ro SH Kim YM Otto NM Cao J Kundu M Kim DH ULK-Atg13-FIP200 complexes mediate mTOR signaling to the autophagy machinery Mol Biol Cell 2009 20 1992 2003 19225151 PMC2663920
- Jung HS Chung KW Won Kim J Kim J Komatsu M Tanaka K Nguyen YH Kang TM Yoon KH Kim JW Loss of autophagy diminishes pancreatic beta cell mass and function with resultant hyperglycemia Cell Metab 2008 8 318 324 18840362
- Kadandale P Kiger AA Role of selective autophagy in cellular remodeling "Self-eating" into shape Autophagy 2010 6 1194 1195 20890115 PMC3359492
- Kalamidas SA Kotoulas OB Glycogen autophagy in newborn rat hepatocytes Histol Histopathol 2000 15 1011 1018 11005224
- Kamada Y Funakoshi T Shintani T Nagano K Ohsumi M Ohsumi Y Tor-mediated induction of autophagy via an Apg1 protein kinase complex J Cell Biol 2000 150 1507 1513 10995454 PMC2150712
- Kaushik S Massey AC Cuervo AM Lysosome membrane lipid microdomains: novel regulators of chaperone-mediated autophagy EMBO J 2006 25 3921 3933 16917501 PMC1560360
- Kaushik S Singh R Cuervo AM Autophagic pathways and metabolic stress Diabetes Obes Metab 2010 12 4 14 21029294 PMC3994321
- Kim J Kundu M Viollet B Guan KL AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1 Nat Cell Biol 2011 13 132 141 21258367 PMC3987946
- Koga H Kaushik S Cuervo AM Altered lipid content inhibits autophagic vesicular fusion FASEB J 2010 24 3052 3065 20375270 PMC2909278
- Komatsu M Waguri S Chiba T Murata S Iwata J Tanida I Ueno T Koike M Uchiyama Y Kominami E Loss of autophagy in the central nervous system causes neurodegeneration in mice Nature 2006 441 880 884 16625205
- Koren I Reem E Kimchi A DAP1, a novel substrate of mTOR, negatively regulates autophagy Curr Biol 2010 20 1093 1098 20537536
- Kovsan J Bluher M Tarnovscki T Kloting N Kirshtein B Madar L Shai I Golan R Harman-Boehm I Schon MR Altered autophagy in human adipose tissues in obesity J Clin Endocrinol Metab 2011 96 E268 E277 21047928
- 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 period Nature 2004 432 1032 1036 15525940
- Lamark T Kirkin V Dikic I Johansen T NBR1 and p62 as cargo receptors for selective autophagy of ubiquitinated targets Cell Cycle 2009 8 1986 1990 19502794
- Lee JH Budanov AV Park EJ Birse R Kim TE Perkins GA Ocorr K Ellisman MH Bodmer R Bier E Sestrin as a feedback inhibitor of TOR that prevents age-related pathologies Science 2010a 327 1223 1228 20203043 PMC2866632
- Lum JJ Bauer DE Kong M Harris MH Li C Lindsten T Thompson CB Growth factor regulation of autophagy and cell survival in the absence of apoptosis Cell 2005 120 237 248 15680329
- Marsh BJ Soden C Alarcon C Wicksteed BL Yaekura K Costin AJ Morgan GP Rhodes CJ Regulated autophagy controls hormone content in secretory-deficient pancreatic endocrine beta-cells Mol Endocrinol 2007 21 2255 2269 17579214
- Marzella L Ahlberg J Glaumann H Autophagy, heterophagy, microautophagy and crinophagy as the means for intracellular degradation Virchows Archiv. B. Cell Pathology 1981 36 219 234 6116336
- Mehrpour M Esclatine A Beau I Codogno P Overview of macroautophagy regulation in mammalian cells Cell Res 2010 20 748 762 20548331
- Mitchener JS Shelburne JD Bradford WD Hawkins HK Cellular autophagocytosis induced by deprivation of serum and amino acids in Hela cells Am J Pathol 1976 83 485 491 937509 PMC2032507
- Mizushima N Levine B Cuervo AM Klionsky DJ Autophagy fights disease through cellular self-digestion Nature 2008 451 1069 1075 18305538 PMC2670399
- Mizushima N Noda T Yoshimori T Tanaka Y Ishii T George MD Klionsky DJ Ohsumi M Ohsumi Y A protein conjugation system essential for autophagy Nature 1998 395 395 398 9759731
- Mizushima N Yamamoto A Matsui M Yoshimori T Ohsumi Y In vivo analysis of autophagy in response to nutrient starvation using transgenic mice expressing a fluorescent autophagosome marker Mol Biol Cell 2004 15 1101 1111 14699058 PMC363084
- Mortimore GE Poso AR Intracellular protein catabolism and its control during nutrient deprivation and supply Annu Rev Nutr 1987 7 539 564 3300746
- Newgard CB An J Bain JR Muehlbauer MJ Stevens RD Lien LF Haqq AM Shah SH Arlotto M Slentz CA A branched-chain amino acid-related metabolic signature that differentiates obese and lean humans and contributes to insulin resistance Cell Metab 2009 9 311 326 19356713 PMC3640280
- Nicklin P Bergman P Zhang B Triantafellow E Wang H Nyfeler B Yang H Hild M Kung C Wilson C Bidirectional transport of amino acids regulates mTOR and autophagy Cell 2009 136 521 534 19203585 PMC3733119
- Nishino I Fu J Tanji K Yamada T Shimojo S Koori T Mora M Riggs J Oh S Koga Y Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease) Nature 2000 406 906 910 10972294
- Onodera J Ohsumi Y Autophagy is required for maintenance of amino acid levels and protein synthesis under nitrogen starvation J Biol Chem 2005 280 31582 31586 16027116
- Raben N Schreiner C Baum R Takikita S Xu S Xie T Myerowitz R Komatsu M Van der Meulen JH Nagaraju K Suppression of autophagy permits successful enzyme replacement therapy in a lysosomal storage disorder--murine Pompe disease Autophagy 2010 6 1078 1089 20861693 PMC3039718
- Ravikumar B Stewart A Kita H Kato K Duden R Rubinsztein DC Raised intracellular glucose concentrations reduce aggregation and cell death caused by mutant huntingtin exon 1 by decreasing mTOR phosphorylation and inducing autophagy Hum Mol Genet 2003 12 985 994 12700167
- Sahu R Kaushik S Cannizzo E Scharf B Follenzi A Clement C Potolicchio I Nieves E Cuervo A Santambrogio L Microautohagy of cytosolic proteins by late endosomes Dev Cell 2011 20 131 139 21238931 PMC3025279
- Sarkar S Davies JE Huang Z Tunnacliffe A Rubinsztein DC Trehalose, a novel mTOR-independent autophagy enhancer, accelerates the clearance of mutant huntingtin and alpha-synuclein J Biol Chem 2007 282 5641 5652 17182613
- Sarkar S Ravikumar B Floto RA Rubinsztein DC Rapamycin and mTOR-independent autophagy inducers ameliorate toxicity of polyglutamine-expanded huntingtin and related proteinopathies Cell Death Differ 2009 16 46 56 18636076
- Schellens JP Vreeling-Sindelarova H Plomp PJ Meijer AJ Hepatic autophagy and intracellular ATP. A morphometric study Exp Cell Res 1988 177 103 108 3391236
- Schworer CM Cox JR Mortimore GE Alteration of lysosomal density by sequestered glycogen during deprivation-induced autophagy in rat liver Biochem Biophys Res Commun 1979 87 163 170 454395
- Shang L Chen S Du F Li S Zhao L Wang X Nutrient starvation elicits an acute autophagic response mediated by Ulk1 dephosphorylation and its subsequent dissociation from AMPK Proc Natl Acad Sci U S A 2011 108 4788 4793 21383122 PMC3064373
- Shibata M Yoshimura K Furuya N Koike M Ueno T Komatsu M Arai H Tanaka K Kominami E Uchiyama Y The MAP1-LC3 conjugation system is involved in lipid droplet formation Biochem Biophys Res Commun 2009 382 419 423 19285958
- Shintani T Yamazaki F Katoh T Umekawa M Matahira Y Hori S Kakizuka A Totani K Yamamoto K Ashida H Glucosamine induces autophagy via an mTOR-independent pathway Biochem Biophys Res Commun 2010 391 1775 1779 20045674
- Singh R Kaushik S Wang Y Xiang Y Novak I Komatsu M Tanaka K Cuervo AM Czaja MJ Autophagy regulates lipid metabolism Nature 2009a 458 1131 1135 19339967 PMC2676208
- Singh R Xiang Y Wang Y Baikati K Cuervo AM Luu YK Tang Y Pessin JE Schwartz GJ Czaja MJ Autophagy regulates adipose mass and differentiation in mice J Clin Invest 2009b 119 3329 3339 19855132 PMC2769174
- Vabulas RM Hartl FU Protein synthesis upon acute nutrient restriction relies on proteasome function Science 2005 310 1960 1963 16373576
- Van Dyke RW Proton pump-generated electrochemical gradients in rat liver multivesicular bodies. Quantitation and effects of chloride J Biol Chem 1988 263 2603 2611 2963813
- Wang J Whiteman MW Lian H Wang G Singh A Huang D Denmark T A non-canonical MEK/ERK signaling pathway regulates autophagy via regulating Beclin 1 J Biol Chem 2009 284 21412 21424 19520853 PMC2755866
- Webber JL Tooze SA Coordinated regulation of autophagy by p38alpha MAPK through mAtg9 and p38IP EMBO J 2010 29 27 40 19893488 PMC2808369
- Wei Y Pattingre S Sinha S Bassik M Levine B JNK1-mediated phosphorylation of Bcl-2 regulates starvation-induced autophagy Mol Cell 2008 30 678 688 18570871 PMC2478643
- Zhang Y Goldman S Baerga R Zhao Y Komatsu M Jin S Adipose-specific deletion of autophagy-related gene 7 (atg7) in mice reveals a role in adipogenesis Proc Natl Acad Sci U S A 2009 106 19860 19865 19910529 PMC2785257
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- Authors
- Singh, R., & Cuervo, A. M.
- Affiliations
- Albert Einstein College of Medicine (US)
- Corresponding author
- Singh, Rajat
- ORCID
- Singh, Rajat
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2011-05
- Volume
- 13
- Issue
- 5
- Pages
- 495-504
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC3099265
- OpenAlex
- W2004325124
- Cited by
- 788
- References
- 11
- Citations by year
- 2026: 21 · 2025: 40 · 2024: 39 · 2023: 37 · 2022: 58 · 2021: 62 · 2020: 78 · 2019: 62 · 2018: 60 · 2017: 48 · 2016: 61 · 2015: 63 · 2014: 44 · 2013: 59 · 2012: 43
- FWCI
- 5.96
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 844 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (AG021904, AG031782, DK041918, DK087776, NS038370)
- Topics
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- autophagy, starvation, lysosomal degradation, protein turnover, organelle turnover, lipid metabolism, carbohydrate metabolism, energy stores, nutrient scarcity
- MeSH terms
- Animals, Autophagy, Cell Membrane, Energy Metabolism, Humans
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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