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The machinery of macroautophagy
Open accessAbstract
Autophagy is a primarily degradative pathway that takes place in all eukaryotic cells. It is used for recycling cytoplasm to generate macromolecular building blocks and energy under stress conditions, to remove superfluous and damaged organelles to adapt to changing nutrient conditions and to maintain cellular homeostasis. In addition, autophagy plays a critical role in cytoprotection by preventing the accumulation of toxic proteins and through its action in various aspects of immunity including the elimination of invasive microbes and its participation in antigen presentation. The most prevalent form of autophagy is macroautophagy, and during this process, the cell forms a double-membrane sequestering compartment termed the phagophore, which matures into an autophagosome. Following delivery to the vacuole or lysosome, the cargo is degraded and the resulting macromolecules are released back into the cytosol for reuse. The past two decades have resulted in a tremendous increase with regard to the molecular studies of autophagy being carried out in yeast and other eukaryotes. Part of the surge in interest in this topic is due to the connection of autophagy with a wide range of human pathophysiologies including cancer, myopathies, diabetes and neurodegenerative disease. However, there are still many aspects of autophagy that remain unclear, including the process of phagophore formation, the regulatory mechanisms that control its induction and the function of most of the autophagy-related proteins. In this review, we focus on macroautophagy, briefly describing the discovery of this process in mammalian cells, discussing the current views concerning the donor membrane that forms the phagophore, and characterizing the autophagy machinery including the available structural information.
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“ATG7 is strictly required for autophagosome formation; it is an E1-like activating enzyme present in ubiquitin-like conjugation systems that promotes both cleavage and lipidation of LC3 and GABARAP [43].”
From A gene toolbox for monitoring autophagy transcription (2021) · cites this paper as [43]
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“ULK1 is considered as the master regulator of autophagy induction, triggering a cascade of signals, through direct phosphorylation of ATG proteins, that culminate in autophagosome formation [3, 43].”
From A gene toolbox for monitoring autophagy transcription (2021) · cites this paper as [43]
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“Indeed, autophagy functions as a quality control mechanism, maintaining cellular homeostasis by destroying aggregate-prone proteins and damaged organelles [45].”
From Unlocking the Therapeutic Potential of Medicinal Plants for Alzheimer’s Disease: Preclinical to Clinical Trial Insights (2023) · cites this paper as [45]
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Cites
AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1
Kim, J., Kundu, M., Viollet, B., & Guan, K.-L. (2011) · Nature Cell Biology · doi:10.1038/ncb2152 · Cited by 7,227
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
Kitada, T., Asakawa, S., Hattori, N., Matsumine, H., Yamamura, Y., Minoshima, S., Yokochi, M., Mizuno, Y., & Shimizu, N. (1998) · Nature · doi:10.1038/33416 · Cited by 5,227
Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue
Duve, C. D., Pressman, B. C., Gianetto, R., Wattiaux, R., & Appelmans, F. (1955) · Biochemical Journal · doi:10.1042/bj0600604 · Cited by 4,176
Autophagy: process and functionPreprint
Mizushima, N. (2007) · Genes & Development · doi:10.1101/gad.1599207 · Cited by 4,104
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Valente, E. M., Abou-Sleiman, P. M., Caputo, V., Muqit, M. M. K., Harvey, K., Gispert, S., Ali, Z., Del Turco, D., Bentivoglio, A. R., Healy, D. G., et al. (2004) · Science · doi:10.1126/science.1096284 · Cited by 3,481
Induction of autophagy and inhibition of tumorigenesis by beclin 1
Liang, X. H., Jackson, S., Seaman, M., Brown, K., Kempkes, B., Hibshoosh, H., & Levine, B. (1999) · Nature · doi:10.1038/45257 · Cited by 3,347
Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273
de Duve, C., & Wattiaux, R. (1966) · Annual Review of Physiology · doi:10.1146/annurev.ph.28.030166.002251 · Cited by 3,033
The Role of Atg Proteins in Autophagosome Formation
Mizushima, N., Yoshimori, T., & Ohsumi, Y. (2011) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-092910-154005 · Cited by 2,978
Autophagy in Health and Disease: A Double-Edged Sword
Shintani, T., & Klionsky, D. J. (2004) · Science · doi:10.1126/science.1099993 · Cited by 2,559
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Yan, S., Wei, X., Xu, S., Sun, H., Wang, W., Liu, L., Jiang, X., Zhang, Y., & Che, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.20757 · Cited by 36
Differential activation of eMI by distinct forms of cellular stress
Mesquita, A., Glenn, J., & Jenny, A. (2020) · Autophagy · doi:10.1080/15548627.2020.1783833 · Cited by 38
Yin, R., Liu, X., Yu, J., Ji, Y., Liu, J., Cheng, L., & Zhou, J. M. (2020) · Scientific Reports · doi:10.1038/s41598-020-68484-3 · Cited by 35
Diceglie, C., Anelli, G. M., Martelli, C., Serati, A., Dico, A. L., Lisso, F., Parisi, F., Novielli, C., Paleari, R., Cetin, I., et al. (2021) · Nutrients · doi:10.3390/nu13041303 · Cited by 37
VHL suppresses RAPTOR and inhibits mTORC1 signaling in clear cell renal cell carcinoma
Ganner, A., Gehrke, C., Klein, M., Thegtmeier, L., Matulenski, T., Wingendorf, L., Wang, L., Pilz, F., Greidl, L., Meid, L., et al. (2021) · Scientific Reports · doi:10.1038/s41598-021-94132-5 · Cited by 39
Gcn5-mediated Rph1 acetylation regulates its autophagic degradation under DNA damage stress
Li, F., Zheng, L., Chen, X., Zhao, X., Briggs, S. D., & Du, H. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx129 · Cited by 35
Crystal structure of NDP52 SKICH region
Pan, L., Fu, T., Liu, J. P., & Xie, X. (2018) · Worldwide Protein Data Bank · doi:10.2210/pdb5z7a/pdb · Cited by 34
Nutrient‐dependent signaling pathways that control autophagy in yeast
Metur, S. P., & Klionsky, D. J. (2023) · FEBS Letters · doi:10.1002/1873-3468.14741 · Cited by 38
Contrasting views on the role of AMPK in autophagy
Kim, D. (2024) · BioEssays · doi:10.1002/bies.202300211 · Cited by 46
Proteostasis in neurodegenerative diseases
Kinger, S., Jagtap, Y. A., Kumar, P., Choudhary, A., Prasad, A., Prajapati, V. K., Kumar, A., Mehta, G., & Mishra, A. (2024) · Advances in clinical chemistry · doi:10.1016/bs.acc.2024.04.002 · Cited by 34
Nicu, C., Hardman, J. A., Pople, J., & Paus, R. (2019) · Experimental Dermatology · doi:10.1111/exd.13904 · Cited by 34
Nettesheim, A., Shim, M. S., Hirt, J., & Liton, P. B. (2019) · Scientific Reports · doi:10.1038/s41598-019-52627-2 · Cited by 34
Gatica, D., Wen, X., Cheong, H., & Klionsky, D. J. (2020) · Autophagy · doi:10.1080/15548627.2020.1776474 · Cited by 34
Nanochaperone‐Based Strategies to Control Protein Aggregation Linked to Conformational Diseases
Caballero, A. B., & Gámez, P. (2020) · Angewandte Chemie International Edition · doi:10.1002/anie.202007924 · Cited by 35
The ATG4 protease integrates redox and stress signals to regulate autophagy
Pérez‐Pérez, M. E., Lemaire, S. D., & Crespo, J. L. (2021) · Journal of Experimental Botany · doi:10.1093/jxb/erab063 · Cited by 34
The Role of Autophagy in Eye Diseases
Fernández‐Albarral, J. A., de Julián-López, E., Soler-Domínguez, C., de Hoz, R., López‐Cuenca, I., Salobrar‐García, E., Ramirez, J. M., Pinazo-Duran, M. D., Salazar, J. J., & Ramirez, A. I. (2021) · Life · doi:10.3390/life11030189 · Cited by 34
H2O2-mediated autophagy during ethanol metabolism
Chen, C., Wang, S., Yu, L., Mueller, J. H., Fortunato, F., Rausch, V., & Mueller, S. (2021) · Redox Biology · doi:10.1016/j.redox.2021.102081 · Cited by 35
Molecular mechanisms of mammalian autophagy
Trelford, C. B., & Guglielmo, G. M. D. (2021) · Biochemical Journal · doi:10.1042/bcj20210314 · Cited by 35
Expanding the view of the molecular mechanisms of autophagy pathway
Majeed, S. T., Majeed, R., & Andrabi, K. I. (2022) · Journal of Cellular Physiology · doi:10.1002/jcp.30819 · Cited by 36
Autophagy/Mitophagy Regulated by Ubiquitination: A Promising Pathway in Cancer Therapeutics
Jee, S.-C., & Cheong, H. (2023) · Cancers · doi:10.3390/cancers15041112 · Cited by 34
Mechanisms of the JNK/p38 MAPK signaling pathway in drug resistance in ovarian cancer
Ma, Y., Li, C., Shen, Y., Wan-hui, Y., Han, M.-X., Mu, Y.-F., & Han, F. (2025) · Frontiers in Oncology · doi:10.3389/fonc.2025.1533352 · Cited by 38
Progressing neurobiological strategies against proteostasis failure: Challenges in neurodegeneration
Amanullah, A., Upadhyay, A., Joshi, V., Mishra, R., Jana, N. R., & Mishra, A. (2017) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2017.08.005 · Cited by 34
Cysteamine-mediated clearance of antibiotic-resistant pathogens in human cystic fibrosis macrophages
Shrestha, C. L., Assani, K. D., Rinehardt, H., Albastroiu, F., Zhang, S., SHELL, R. D., Amer, A. O., Schlesinger, L. S., & Kopp, B. T. (2017) · PLoS ONE · doi:10.1371/journal.pone.0186169 · Cited by 33
Zientara‐Rytter, K., Ozeki, K. A., Nazarko, T. Y., & Subramani, S. E. (2017) · Autophagy · doi:10.1080/15548627.2017.1413521 · Cited by 33
Autophagy in turnover of lipid stores: trans-kingdom comparison
Elander, P. H., Minina, E. A., & Bozhkov, P. V. (2017) · Journal of Experimental Botany · doi:10.1093/jxb/erx433 · Cited by 34
Therapeutic Potential of Autophagy Modulation in Cholangiocarcinoma
Perez‐Montoyo, H. (2020) · Cells · doi:10.3390/cells9030614 · Cited by 35
How Can Malnutrition Affect Autophagy in Chronic Heart Failure? Focus and Perspectives
Corsetti, G., Pasini, E., Romano, C., Chen-Scarabelli, C. A., Scarabelli, T. M., Flati, V., Saravolatz, L. I. I., & Dioguardi, F. S. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073332 · Cited by 33
Xu, C., Zang, Y., Zhao, Y., Cui, W., Zhang, H., Zhu, Y., & Xu, M. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.652211 · Cited by 34
Autophagy and senescence in cancer therapy
Patel, N. H., Bloukh, S., Alwohosh, E., Alhesa, A., Saleh, T., & Gewirtz, D. A. (2021) · Advances in cancer research · doi:10.1016/bs.acr.2021.01.002 · Cited by 36
The Impact of Aging on Macroautophagy in the Pre-ovulatory Mouse Oocyte
Peters, A. E., Caban, S., McLaughlin, E. A., Roman, S. D., Bromfield, E. G., Nixon, B., & Sutherland, J. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.691826 · Cited by 33
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Hung, S. W., Li, Y., Chen, X., Chu, K. O., Zhao, Y., Liu, Y., Guo, X. W., Man, G. C. W., & Wang, C. C. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.906746 · Cited by 33
Xie, X., Hu, L., Mi, B., Xue, H., Xiong, Y., Hu, Y., Panayi, A. C., Endo, Y., Chen, L., Yan, C., et al. (2022) · Cell Communication and Signaling · doi:10.1186/s12964-022-00966-5 · Cited by 35
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Al‐Odat, O. S., Guirguis, D. A., Schmalbach, N. K., Yao, G., Budak-Alpdoǧan, T., Jonnalagadda, S. C., & Pandey, M. K. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010644 · Cited by 34
Kumar, A., Girisa, S., Alqahtani, M. S., Abbas, M. A. E., Hegde, M., Sethi, G., & Kunnumakkara, A. B. (2023) · Cells · doi:10.3390/cells12050810 · Cited by 34
Molecular regulation and therapeutic implications of cell death in pulmonary hypertension
Wang, E., Zhou, S., Zeng, D., & Wang, R. (2023) · Cell Death Discovery · doi:10.1038/s41420-023-01535-6 · Cited by 33
Lamacchia, M., Dyrka, W., Breton, A. M., Saupe, S. J., & Paoletti, M. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00471 · Cited by 33
Raffa, S., Forte, M., Gallo, G., Ranieri, D., Marchitti, S., Magrì, D., Testa, M., Stanzione, R., Bianchi, F., Cotugno, M., et al. (2023) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-04777-w · Cited by 33
Role of Macroautophagy in Mammalian Male Reproductive Physiology
Kirat, D., Alahwany, A. M., Arisha, A. H., Abdelkhalek, A., & Miyasho, T. (2023) · Cells · doi:10.3390/cells12091322 · Cited by 34
Autophagy orchestrates the crosstalk between cells and organs
Piletič, K., Alsaleh, G., & Simon, A. K. (2023) · EMBO Reports · doi:10.15252/embr.202357289 · Cited by 31
Lin, J., Chen, R., Yang, L., Gong, M., Du, M.-Y., Mu, S.-Q., Jiang, Z.-A., Li, H., Yang, Y., Wang, X., et al. (2023) · Journal of Advanced Research · doi:10.1016/j.jare.2023.07.010 · Cited by 31
An, F., Zhang, J., Gao, P., Xiao, Z., Chang, W., Song, J., Wang, Y., Ma, H., Zhang, R., Chen, Z., et al. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1297024 · Cited by 34
Accumulation of F-actin drives brain aging and limits healthspan in Drosophila
Schmid, E. T., Schinaman, J. M., Liu-Abramowicz, N., Williams, K. S., & Walker, D. W. (2024) · Nature Communications · doi:10.1038/s41467-024-53389-w · Cited by 35
Insulin Regulation of Myocardial Autophagy
Riehle, C., & Abel, E. D. (2014) · Circulation Journal · doi:10.1253/circj.cj-14-1080 · Cited by 32
The carbon starvation response of the ectomycorrhizal fungus Paxillus involutus
Ellström, M., Shah, F., Johansson, T., Ahrén, D., Persson, P., & Tunlid, A. (2015) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiv027 · Cited by 32
Shi, Q., Zhang, Q., Peng, Y., Zhang, X., Wang, Y., & Shi, L. (2019) · Journal of Pharmacy and Pharmacology · doi:10.1111/jphp.13096 · Cited by 32
Pan, X., Neufeld, T. P., & O’Connor, M. B. (2019) · Current Biology · doi:10.1016/j.cub.2019.07.027 · Cited by 32
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Shi, R., Fu, Y., Zhao, D., Boczek, T., Wang, W., & Guo, F. (2021) · Biochemical Pharmacology · doi:10.1016/j.bcp.2021.114664 · Cited by 35
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Fruiting-Body Development in Ascomycetes
Pöggeler, S., Nowrousian, M., Teichert, I., Beier, A., & Kück, U. (2018) · Springer eBooks · doi:10.1007/978-3-319-71740-1_1 · Cited by 37
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Zhu, Z., Liu, L., Su, C.-F., Liu, J., Tong, B. C., Iyaswamy, A., Krishnamoorthi, S., Sreenivasmurthy, S. G., Guan, X.-J., Kan, Y., et al. (2022) · Acta Pharmacologica Sinica · doi:10.1038/s41401-022-00871-0 · Cited by 33
Khan, S., Mentrup, H. L., Novak, E. A., Siow, V. S., Wang, Q., Crawford, E. C., Schneider, C., Comerford, T. E., Firek, B., Rogers, M. B., et al. (2022) · The FASEB Journal · doi:10.1096/fj.202200138r · Cited by 32
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Titone, R., Morani, F., Follo, C., Vidoni, C., Mezzanzanica, D., & Isidoro, C. (2014) · BioMed Research International · doi:10.1155/2014/343542 · Cited by 33
Upadhyay, A. (2021) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2021.01.006 · Cited by 31
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Chang, L., Chiang, S.-K., Chen, S., & Hung, M. (2024) · Journal of Biomedical Science · doi:10.1186/s12929-024-01089-4 · Cited by 36
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Bellelli, F., Angioni, D., Arosio, B., Vellas, B. J., & Barreto, P. D. S. (2025) · Ageing Research Reviews · doi:10.1016/j.arr.2025.102699 · Cited by 34
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Zhen, X., Xu, F., Zhang, W., Li, N., & Li, X. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223011 · Cited by 31
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Mu, W., Rezek, V. K., Martin, H. A., Carrillo, M. A., Tomer, S., Hamid, P., Lizarraga, M. A., Tibbe, T. D., Yang, O. O., Jamieson, B. D., et al. (2021) · JCI Insight · doi:10.1172/jci.insight.159136 · Cited by 31
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Xiang, H., Zhou, M., Li, Y., Zhou, L., & Wang, R. (2023) · Acta Pharmaceutica Sinica B · doi:10.1016/j.apsb.2023.07.016 · Cited by 31
Tan, T., Zimmermann, M., & Reichert, A. S. (2016) · Biological Chemistry · doi:10.1515/hsz-2016-0125 · Cited by 33
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Loos, B., Klionsky, D. J., du Toit, A., & Hofmeyr, J. S. (2019) · Autophagy · doi:10.1080/15548627.2019.1687211 · Cited by 32
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Liu, Y., Luo, X., Shan, H., Fu, Y., Gu, Q., Zheng, X., Dai, Q., Xia, F., Zheng, Z., Liu, P., et al. (2019) · Cells · doi:10.3390/cells8030248 · Cited by 30
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Metadata
- Authors
- Feng, Y., He, D., Yao, Z., & Klionsky, D. J.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Klionsky, Daniel J
- Venue
- Cell Research
- Published
- 2013-12-24
- Volume
- 24
- Issue
- 1
- Pages
- 24-41
- ISSN
- 1001-0602 (ISSN-L)
- 1748-7838
- PMC
- PMC3879710
- OpenAlex
- W2044621729
- Cited by
- 2,083
- References
- 180
- Citations by year
- 2026: 84 · 2025: 130 · 2024: 193 · 2023: 180 · 2022: 238 · 2021: 215 · 2020: 200 · 2019: 185 · 2018: 177 · 2017: 161 · 2016: 161 · 2015: 109 · 2014: 45 · 2013: 3
- FWCI
- 12.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Cell Research (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of General Medical Sciences (R01GM053396)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- macroautophagy, autophagy machinery, phagophore formation, autophagosomes, autophagy-related proteins, autophagy regulation, lysosomes, cellular homeostasis, cytoprotection, neurodegenerative diseases, cancer, yeast autophagy
- MeSH terms
- Animals, Autophagy, Homeostasis, Humans, Lysosomes, Phagosomes, Pichia, Saccharomyces cerevisiae, Vacuoles, Protein Serine-Threonine Kinases
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