Autophagy‐based unconventional secretory pathway for extracellular delivery of IL‐1β

Repertoires of Autophagy in the Pathogenesis of Ocular Diseases

Li, Y., Jiang, Q. L., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,351

AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1

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Autophagy fights disease through cellular self-digestion

Mizushima, N., Levine, B., Cuervo, A. M., & Klionsky, D. J. (2008) · Nature · doi:10.1038/nature06639 · Cited by 6,452

A role for mitochondria in nlrp3 inflammasome activation

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Gout-associated uric acid crystals activate the NALP3 inflammasome

Martinon, F., Pétrilli, V., Mayor, A., Tardivel, A., & Tschopp, J. (2006) · Nature · doi:10.1038/nature04516 · Cited by 5,326

Methods in Mammalian Autophagy Research

Mizushima, N., Yoshimori, T., & Levine, B. (2010) · Cell · doi:10.1016/j.cell.2010.01.028 · Cited by 4,497

Antimicrobial Autophagy: A Conserved Innate Immune Response in Drosophila

Moy, R. H., & Cherry, S. R. (2013) · Journal of Innate Immunity · doi:10.1159/000350326 · Cited by 3,551

Autophagy and the Integrated Stress Response

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Autophagy in immunity and inflammation

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Mechanisms of mitophagy

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Enhanced Therapeutic Efficacy in Cancer Patients by Short-term Fasting: The Autophagy Connection

van Niekerk, G., Hattingh, S. M., & Engelbrecht, A. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00242 · Cited by 29

Early endosome autoantigen 1 regulates IL-1β release upon caspase-1 activation independently of gasdermin D membrane permeabilization

Baroja‐Mazo, A., Compan, V., Martín‐Sánchez, F., Tapia‐Abellán, A., Couillin, I., & Pelegrı́n, P. (2019) · Scientific Reports · doi:10.1038/s41598-019-42298-4 · Cited by 30

Extracellular HSPs: The Potential Target for Human Disease Therapy

Li, D.-Y., Liang, S., Wen, J.-H., Tang, J., Deng, S., & Liu, Y. (2022) · Molecules · doi:10.3390/molecules27072361 · Cited by 30

Autophagy-Related Pathways in Vesicular Unconventional Protein Secretion

Noh, S. H., Kim, Y. J., & Lee, M. G. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.892450 · Cited by 29

Diverse Control Mechanisms of the Interleukin-1 Cytokine Family

Evavold, C. L., & Kagan, J. C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.910983 · Cited by 34

TBK1 phosphorylation activates LIR-dependent degradation of the inflammation repressor TNIP1

Zhou, J., Rasmussen, N. L., Olsvik, H. L., Akimov, V., Hu, Z., Evjen, G., Kaeser-Pebernard, S., Sankar, D. S., Roubaty, C., Verlhac, P., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202108144 · Cited by 28

Crosstalk Between Cell Death and Spinal Cord Injury: Neurology and Therapy

Song, Q., Cui, Q., Sun, S., Wang, Y., Yin, Y., & Zhang, L. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04188-3 · Cited by 30

Tissue‐Adaptive BSA Hydrogel with Dual Release of PTX and bFGF Promotes Spinal Cord Injury Repair via Glial Scar Inhibition and Axon Regeneration

Zhu, S., Wu, Q., Ying, Y., Mao, Y., Lu, W., Xu, J., Cai, X., He, H., & Wu, J. (2024) · Small · doi:10.1002/smll.202401407 · Cited by 31

Aged kidney: can we protect it? Autophagy, mitochondria and mechanisms of ischemic preconditioning

Jankauskas, S. S., Silachev, D. N., Andrianova, N. V., Pevzner, I. B., Zorova, L. D., Popkov, V. A., Plotnikov, E. Y., & Zorov, D. B. (2018) · Cell Cycle · doi:10.1080/15384101.2018.1482149 · Cited by 28

Proteasome 19S RP and translation preinitiation complexes are secreted within exosomes upon serum starvation

Bec, N., Bonhoure, A., Henry, L., Berry, L., Larroque, C., Coux, O., Stoebner, P., & Vidal, M. (2019) · Traffic · doi:10.1111/tra.12653 · Cited by 28

Autophagy in the HTR‐8/SVneo Cell Oxidative Stress Model Is Associated with the NLRP1 Inflammasome

Li, M., Sun, T., Wu, X., An, P., Wu, X., & Dang, H. (2021) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2021/2353504 · Cited by 28

Nrf2 Pathway and Autophagy Crosstalk: New Insights into Therapeutic Strategies for Ischemic Cerebral Vascular Diseases

Hu, Y. H., Luo, Y., & Zheng, Y. (2022) · Antioxidants · doi:10.3390/antiox11091747 · Cited by 29

Emerging roles of mitochondria and autophagy in liver injury during sepsis

Aki, T., Unuma, K., & Uemura, K. (2017) · Cell Stress · doi:10.15698/cst2017.11.110 · Cited by 28

Differential Radiation Sensitivity in p53 Wild-Type and p53-Deficient Tumor Cells Associated with Senescence but not Apoptosis or (Nonprotective) Autophagy

Xu, J., Patel, N. H., Saleh, T., Cudjoe, E. K., Alotaibi, M. R., Wu, Y., Lima, S., Hawkridge, A. M., & Gewirtz, D. A. (2018) · Radiation Research · doi:10.1667/rr15099.1 · Cited by 28

Secretory autophagy holds the key to lysozyme secretion during bacterial infection of the intestine

Delorme‐Axford, E., & Klionsky, D. J. (2017) · Autophagy · doi:10.1080/15548627.2017.1401425 · Cited by 28

Autophagy and Inflammation: Regulatory Roles in Viral Infections

Chen, L., Yang, L., Li, Y., Liu, T., Yang, B., Liu, L., & Wu, R. (2023) · Biomolecules · doi:10.3390/biom13101454 · Cited by 29

Extracellular vesicles: biogenesis mechanism and impacts on tumor immune microenvironment

Yeat, N. Y., & Chen, R. (2025) · Journal of Biomedical Science · doi:10.1186/s12929-025-01182-2 · Cited by 32

Autophagy: Basic Principles and Relevance to Transplant Immunity

Bizargity, P., & Schröppel, B. (2014) · American Journal of Transplantation · doi:10.1111/ajt.12743 · Cited by 27

Endothelial acid ceramidase in exosome-mediated release of NLRP3 inflammasome products during hyperglycemia: Evidence from endothelium-specific deletion of Asah1 gene

Yuan, X., Bhat, O. M., Lohner, H., Zhang, Y., & Li, P. (2019) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2019.158532 · Cited by 27

Vying for the control of inflammasomes: The cytosolic frontier of enteric bacterial pathogen–host interactions

Sanchez‐Garrido, J., Slater, S. L., Clements, A., Shenoy, A. R., & Frankel, G. M. (2020) · Cellular Microbiology · doi:10.1111/cmi.13184 · Cited by 24

Secretory function of autophagy in innate immune cells

Bhattacharya, A., Prakash, Y. S., & Eissa, N. T. (2014) · Cellular Microbiology · doi:10.1111/cmi.12365 · Cited by 27

Tumor necrosis factor receptor-associated periodic syndrome as a model linking autophagy and inflammation in protein aggregation diseases

Bachetti, T., & Ceccherini, I. (2014) · Journal of Molecular Medicine · doi:10.1007/s00109-014-1150-5 · Cited by 27

How to use a multipurpose SNARE: The emerging role of Snap29 in cellular health

Mastrodonato, V., Morelli, E., & Vaccari, T. (2018) · Cell Stress · doi:10.15698/cst2018.04.130 · Cited by 27

Grasp55−/− mice display impaired fat absorption and resistance to high-fat diet-induced obesity

Kim, J., Kim, H., Noh, S. H., Jang, D. G., Park, S., Min, D., Kim, H., Kweon, H., Kim, H., Aum, S., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14912-x · Cited by 27

Prelysosomal Compartments in the Unconventional Secretion of Amyloidogenic Seeds

Madsen, H. B., & Vilhardt, F. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010227 · Cited by 26

Beyond Self-Recycling: Cell-Specific Role of Autophagy in Atherosclerosis

Henderson, J. M., Weber, C., & Santovito, D. (2021) · Cells · doi:10.3390/cells10030625 · Cited by 27

Selective autophagy against membranous compartments

Pimentel‐Muiños, F. X., & Boada-Romero, E. (2014) · Autophagy · doi:10.4161/auto.27244 · Cited by 26

Canonical autophagy does not contribute to cellular radioresistance

Schaaf, M. B. E., Jutten, B., Keulers, T. G., Savelkouls, K. G. M., Peeters, H. J. M., van den Beucken, T., van Schooten, F., Godschalk, R., Vooijs, M., & Rouschop, K. M. A. (2015) · Radiotherapy and Oncology · doi:10.1016/j.radonc.2015.02.019 · Cited by 26

The Unfolded Protein Response Regulates an Angiogenic Response by the Kidney Epithelium during Ischemic Stress

Bouvier, N., Fougeray, S., Beaune, P. H., Thervet, É., & Pallet, N. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.340570 · Cited by 30

The unconventional secretion of ARMS2

Körtvely, E., Hauck, S. M., Behler, J., Ho, N., & Ueffing, M. (2016) · Human Molecular Genetics · doi:10.1093/hmg/ddw162 · Cited by 26

Homeostatic Role of Autophagy in Hepatocytes

Khambu, B., Yan, S., Huda, N., Liu, G., & Yin, X. (2018) · Seminars in Liver Disease · doi:10.1055/s-0038-1669939 · Cited by 28

Purple sweet potato color attenuated NLRP3 inflammasome by inducing autophagy to delay endothelial senescence

Sun, C., Diao, Q., Lü, J., Zhang, Z., Wu, D., Wang, X., Xie, J., Zheng, G., Shan, Q., Fan, S., et al. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.28003 · Cited by 25

Induction of autophagy protects human dental pulp cells from lipopolysaccharide‑induced pyroptotic cell death

Gao, Y., You, X., Liu, Y., Gao, F., Zhang, Y., Yang, J., & Yang, C. G. (2020) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2020.8475 · Cited by 25

Facets of Autophagy Based Unconventional Protein Secretion–The Road Less Traveled

Padmanabhan, S., & Manjithaya, R. R. (2020) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2020.586483 · Cited by 25

The physiological and pathophysiological roles of the autophagy lysosomal system in the conventional aqueous humor outflow pathway: More than cellular clean up

Shim, M. S., & Liton, P. B. (2022) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2022.101064 · Cited by 27

Cytosolic HMGB1 Mediates LPS-Induced Autophagy in Microglia by Interacting with NOD2 and Suppresses Its Proinflammatory Function

Kim, S., Oh, S.-A., Seol, S.-I., Davaanyam, D., & Lee, J.-K. (2022) · Cells · doi:10.3390/cells11152410 · Cited by 25

New iron export pathways acting via holo-ferritin secretion

Yanatori, I., Kishi, F., & Toyokuni, S. (2023) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2023.109737 · Cited by 28

Neuronal activity promotes secretory autophagy for the extracellular release of α-synuclein

Nakamura, Y., Sawai, T., Kakiuchi, K., & Arawaka, S. (2024) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2024.107419 · Cited by 25

Variants of Porphyromonas gingivalis lipopolysaccharide alter lipidation of autophagic protein, microtubule‐associated protein 1 light chain 3, LC3

Blasi, I., Korostoff, J. M., Dhingra, A., Reyes-Reveles, J., Shenker, B. J., Shahabuddin, N., Alexander, D., Lally, E. T., Bragin, A., & Boesze‐Battaglia, K. (2015) · Molecular Oral Microbiology · doi:10.1111/omi.12141 · Cited by 26

High Serum HDGF Levels Are Predictive of Bone Metastasis and Unfavorable Prognosis in Non-Small Cell Lung Cancer

Zhang, G., Liu, Z., Chen, Y., & Zhang, Y. (2017) · The Tohoku Journal of Experimental Medicine · doi:10.1620/tjem.242.101 · Cited by 25

An Amish founder mutation disrupts a PI(3)P-WHAMM-Arp2/3 complex–driven autophagosomal remodeling pathway

Mathiowetz, A. J., Baple, E., Russo, A. J., Coulter, A. M., Carrano, E., Brown, J. D., Jinks, R. N., Crosby, A. H., & Campellone, K. G. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e17-01-0022 · Cited by 29

Autophagy dysfunction in autoinflammatory diseases

Hua, Y., Shen, M., McDonald, C., & Yao, Q. (2017) · Journal of Autoimmunity · doi:10.1016/j.jaut.2017.10.012 · Cited by 24

BRF1 ameliorates LPS-induced inflammation through autophagy crosstalking with MAPK/ERK signaling

Xie, W., Zheng, W., Liu, M., Qin, Q., Zhao, Y., Cheng, Z., & Guo, F. (2018) · Genes & Diseases · doi:10.1016/j.gendis.2018.04.004 · Cited by 24

Effects of mineral trioxide aggregate and bioceramics on macrophage differentiation and polarization in vitro

Tu, M., Sun, K.-T., Wang, T., He, Y.-Z., Hsia, S., Tsai, B.-H., Shih, Y.-H., & Shieh, T. (2019) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2019.07.010 · Cited by 26

Efferocytosis Drives Myeloid NLRP3 Dependent Inflammasome Signaling and Gasdermin D Independent Secretion of IL-1β to Promote Tumor Growth

Lang, C., Roy, S., Wang, Y., Graves, D. K., Xu, Y., Serezani, C. H., Korrer, M. J., & Kim, Y. J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.993771 · Cited by 24

Coronavirus envelope protein activates TMED10-mediated unconventional secretion of inflammatory factors

Liu, L., Zhang, L., Hao, X., Wang, Y., Zhang, X., Ge, L., Wang, P., Tian, B., & Zhang, M. (2024) · Nature Communications · doi:10.1038/s41467-024-52818-0 · Cited by 26

MERTK-Mediated LC3-Associated Phagocytosis (LAP) of Apoptotic Substrates in Blood-Separated Tissues: Retina, Testis, Ovarian Follicles

Yéfimova, M., Ravel, C., Rolland, A. D., Bourmeyster, N., & Jégou, B. (2021) · Cells · doi:10.3390/cells10061443 · Cited by 24

Osteocytes Enhance Osteogenesis by Autophagy-Mediated FGF23 Secretion Under Mechanical Tension

Xu, H., Xia, M., Sun, L., Wang, H., & Zhang, W. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.782736 · Cited by 26

Canonical and Non-Canonical Functions of the Autophagy Machinery in MHC Restricted Antigen Presentation

Münz, C. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.868888 · Cited by 26

Targeting autophagy regulation in NLRP3 inflammasome-mediated lung inflammation in COVID-19

Yong, Y.-Y., Zhang, L., Hu, Y.-J., Wu, J., Yan, L., Pan, Y., Tang, Y., Yu, L., Law, B. Y. K., Yu, C., et al. (2022) · Clinical Immunology · doi:10.1016/j.clim.2022.109093 · Cited by 25

S100A10 Regulates ULK1 Localization to ER–Mitochondria Contact Sites in IFN-γ-Triggered Autophagy

Chen, Y.-D., Fang, Y.-T., Chang, C., Lin, C., Hsu, L., Wu, S.-R., Chiu, Y., Anderson, R., & Lin, Y.-S. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.11.009 · Cited by 23

A Vibrio vulnificus VvpM Induces IL-1β Production Coupled with Necrotic Macrophage Death via Distinct Spatial Targeting by ANXA2

Lee, S., Jung, Y. H., Kim, J. S., Lee, H. J., Lee, S. H., Lee, K., Jang, K. K., Choi, S. H., & Han, H. J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00352 · Cited by 24

Provocative decompression causes diffuse vascular injury in mice mediated by microparticles containing interleukin-1β

Thom, S. R., Bhopale, V. M., Yu, K., & Yang, M. (2018) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00620.2018 · Cited by 25

Unconventional secretion factor GRASP55 is increased by pharmacological unfolded protein response inducers in neurons

van Ziel, A. M., Largo‐Barrientos, P., Wolzak, K., Verhage, M., & Scheper, W. (2019) · Scientific Reports · doi:10.1038/s41598-018-38146-6 · Cited by 24

Autophagy, innate immunity, and cardiac disease

Santovito, D., Steffens, S., Barachini, S., & Madonna, R. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1149409 · Cited by 25

Granzyme B degrades extracellular matrix and promotes inflammation and choroidal neovascularization

Obasanmi, G., Uppal, M., Cui, J. Z., Xi, J., Ju, M. J., Song, J. L., To, E. C., Li, S., Khan, W., Cheng, D., et al. (2024) · Angiogenesis · doi:10.1007/s10456-024-09909-9 · Cited by 25

Targeting secretory autophagy in solid cancers: mechanisms, immune regulation and clinical insights

Li, X., & Zhao, H. (2025) · Experimental Hematology and Oncology · doi:10.1186/s40164-025-00603-0 · Cited by 25

Soybean Peptide QRPR Activates Autophagy and Attenuates the Inflammatory Response in the RAW264.7 Cell Model

Pan, F., Wang, L., Cai, Z., Wang, Y., Wang, Y., Guo, J., Xu, X., & Zhang, X. (2019) · Protein and Peptide Letters · doi:10.2174/0929866526666190124150555 · Cited by 23

MEHP induces pyroptosis and autophagy alternation by cathepsin B activation in INS-1 cells

Jiang, L., Qiu, T., Yao, X., Chen, H., Yao, K., Sun, X., Yang, G., Jiang, L., Zhang, C., Wang, N., et al. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-14997-x · Cited by 23

Ubiquitination-Dependent Regulation of Small GTPases in Membrane Trafficking: From Cell Biology to Human Diseases

Lei, Z., Wang, J., Zhang, L., & Liu, C. H. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.688352 · Cited by 22

New insights into the role of the Golgi apparatus in the pathogenesis and therapeutics of human diseases

Choi, W., Kang, S., & Kim, J. (2022) · Archives of Pharmacal Research · doi:10.1007/s12272-022-01408-z · Cited by 24

Regulation of innate immunity by the molecular machinery of macroautophagy

Münz, C. (2014) · Cellular Microbiology · doi:10.1111/cmi.12358 · Cited by 23

Clinical application: Restoration of immune homeostasis by autophagy as a potential therapeutic target in sepsis

Zhang, L., Ai, Y., & Tsung, A. (2016) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2016.3071 · Cited by 23

Reflections on the role of senescence during development and aging

Triana-Martínez, F., Pedraza-Vázquez, G., Maciel-Barón, L. Á., & Königsberg, M. (2016) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2016.04.004 · Cited by 23

The unconventional secretion of PepN is independent of a functional autophagy machinery in the filamentous fungusAspergillus niger

Burggraaf, A., Punt, P. J., & Ram, A. F. J. (2016) · FEMS Microbiology Letters · doi:10.1093/femsle/fnw152 · Cited by 23

Role of Autophagy in HIV-1 Matrix Protein p17-Driven Lymphangiogenesis

Mazzuca, P., Marsico, S., Schulze, K., Mitola, S. M. F., Pils, M. C., Giagulli, C., Guzmán, C. A., Caruso, A., & Caccuri, F. (2017) · Journal of Virology · doi:10.1128/jvi.00801-17 · Cited by 23

Autophagy Proteins in Viral Exocytosis and Anti-Viral Immune Responses

Münz, C. (2017) · Viruses · doi:10.3390/v9100288 · Cited by 23

Post-translational modifications of ATG8 proteins – an emerging mechanism of autophagy control

Nieto-Torres, J. L., Zaretski, S., Liu, T., Adams, P. D., & Hansen, M. (2023) · Journal of Cell Science · doi:10.1242/jcs.259725 · Cited by 23

Application of Gaussia luciferase in bicistronic and non-conventional secretion reporter constructs

Luft, C., Freeman, J., Elliott, D. J. S., Al‐Tamimi, N., Kriston-Vizi, J., Heintze, J., Lindenschmidt, I., Seed, B., & Ketteler, R. (2014) · BMC Biochemistry · doi:10.1186/1471-2091-15-14 · Cited by 23

Basal Autophagy Is Altered in Lagotto Romagnolo Dogs with an ATG4D Mutation

Syrjä, P., Anwar, T., Jokinen, T. S., Kyöstilä, K., Jäderlund, K. H., Cozzi, F., Rohdin, C., Hahn, K., Wohlsein, P., Baumgärtner, W., et al. (2017) · Veterinary Pathology · doi:10.1177/0300985817712793 · Cited by 21

Autophagy in immunity

Münz, C. (2020) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2020.03.005 · Cited by 23

Pik3c3 deficiency in myeloid cells imparts partial resistance to experimental autoimmune encephalomyelitis associated with reduced IL-1β production

Yang, G., Song, W., Xu, J., Postoak, J. L., Cheng, F., Martinez, J., Zhang, J., Wu, L., & Kaer, L. V. (2020) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-00589-1 · Cited by 23

Kir6.2 knockout aggravates lipopolysaccharide-induced mouse liver injury via enhancing NLRP3 inflammasome activation

Du, R., Tan, J., Yan, N., Wang, X., Qiao, C., Ding, J., Lu, M., & Hu, G. (2013) · Journal of Gastroenterology · doi:10.1007/s00535-013-0823-0 · Cited by 22

The impact of macroautophagy on CD 8+ T‐cell‐mediated antiviral immunity

Pérot, B. P., Ingersoll, M. A., & Albert, M. L. (2013) · Immunological Reviews · doi:10.1111/imr.12096 · Cited by 23

Regulation of inflammatory processes by caspases

Beltrán‐Visiedo, M., Soler-Agesta, R., Sarosiek, K. A., Green, D. R., & Galluzzi, L. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00869-6 · Cited by 23

The Macroautophagy Machinery in Endo- and Exocytosis

Münz, C. (2016) · Journal of Molecular Biology · doi:10.1016/j.jmb.2016.11.028 · Cited by 20

Autonomous Non Antioxidant Roles for Fasciola hepatica Secreted Thioredoxin-1 and Peroxiredoxin-1

Dorey, A., Cwiklinski, K., Rooney, J., Veríssimo, C. D. M., Corrales, J. L., Jewhurst, H., Fazekas, B., Calvani, N. E. D., Hamon, S., Gaughan, S., et al. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.667272 · Cited by 19

The ATG5 interactome links clathrin-mediated vesicular trafficking with the autophagosome assembly machinery

Baines, K., Yoshioka, K., Takuwa, Y., & Lane, J. D. (2022) · Autophagy Reports · doi:10.1080/27694127.2022.2042054 · Cited by 24

mTOR-Mediated Autophagy Regulates Fumonisin B1-Induced Intestinal Inflammation via Pyroptosis In Vivo and In Vitro

Mao, X., Liu, S., Ge, L., Du, H., Yue, D., Hou, L., Huang, K., & Chen, X. (2022) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.2c03025 · Cited by 21

A noncanonical function of SKP1 regulates the switch between autophagy and unconventional secretion

Li, J., Krause, G. J., Gui, Q., Kaushik, S., Róna, G., Zhang, Q., Liang, F., Dhabaria, A., Anerillas, C., Martindale, J. L., et al. (2023) · Science Advances · doi:10.1126/sciadv.adh1134 · Cited by 21

Algal oil rich in n-3 polyunsaturated fatty acids suppresses B16F10 melanoma lung metastasis by autophagy induction

Tan, R.-H., Wang, F., Fan, C., Zhang, X., Zhao, J., Zhang, J., Yang, Y., Yang, X., Zou, Z., & Bu, S. (2018) · Food & Function · doi:10.1039/c8fo01617h · Cited by 23

Heparanase Involvement in Exosome Formation

David, G., & Zimmermann, P. (2020) · Advances in experimental medicine and biology · doi:10.1007/978-3-030-34521-1_10 · Cited by 21

The Autophagosomes Containing Dengue Virus Proteins and Full-Length Genomic RNA Are Infectious

Wu, S., Chen, Y., Lee, Y., Lin, C., Lan, S., Lan, K.-Y., Chu, M., Lin, P., Yang, Z.-L., Chen, Y., et al. (2021) · Viruses · doi:10.3390/v13102034 · Cited by 22

Energetic Stress‐Induced Metabolic Regulation by Extracellular Vesicles

Crewe, C. (2023) · Comprehensive physiology · doi:10.1002/cphy.c230001 · Cited by 48

Salicylic acid is a key player of Arabidopsis autophagy mutant susceptibility to the necrotrophic bacterium Dickeya dadantii

Rigault, M., Citerne, S., Masclaux‐Daubresse, C., & Dellagi, A. (2021) · Scientific Reports · doi:10.1038/s41598-021-83067-6 · Cited by 20

Non-autophagy Role of Atg5 and NBR1 in Unconventional Secretion of IL-12 Prevents Gut Dysbiosis and Inflammation

Merkley, S. D., Goodfellow, S. M., Guo, Y. P., Wilton, Z. E. R., Byrum, J. R., Schwalm, K. C., Dinwiddie, D. L., Gullapalli, R. R., Deretic, V. P., Hernández, A. J., et al. (2021) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjab144 · Cited by 20

Complexities of JC Polyomavirus Receptor-Dependent and -Independent Mechanisms of Infection

Morris‐Love, J., & Atwood, W. J. (2022) · Viruses · doi:10.3390/v14061130 · Cited by 21

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