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

Kim, J., Kundu, M., Viollet, B., & Guan, K.-L. (2011) · Nature Cell Biology · doi:10.1038/ncb2152 · Cited by 7,227

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

Zhou, R., Yazdi, A. S., Menu, P., & Tschopp, J. (2011) · Nature · doi:10.1038/nature09663 · Cited by 5,602

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

Kroemer, G., Mariño, G., & Levine, B. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.09.023 · Cited by 3,506

Autophagy in immunity and inflammation

Levine, B., Mizushima, N., & Virgin, H. W. (2011) · Nature · doi:10.1038/nature09782 · Cited by 3,289

Mechanisms of mitophagy

Youle, R. J., & Narendra, D. P. (2011) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3028 · Cited by 3,273

Autophagy induced by Helicobacter Pylori infection can lead to gastric cancer dormancy, metastasis, and recurrence: new insights

Akbari, A., Varnosfaderani, S. M. N., Haeri, M. S., Fathi, Z., Aziziyan, F., Rad, A. Y., Zalpoor, H., Nabi‐Afjadi, M., & Malekzadegan, Y. (2023) · Human Cell · doi:10.1007/s13577-023-00996-2 · Cited by 18

The role of high‐mobility group protein box 1 in lung cancer

Wu, X., Chen, Y., Gong, C., & Pei, D. (2018) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26837 · Cited by 18

Identification of Rabbit Oviductal Fluid Proteins Involved in Pre‐Fertilization Processes by Quantitative Proteomics

Yu, H., Hackenbroch, L., Meyer, F. R. L., Reiser, J., Razzazi‐Fazeli, E., Nöbauer, K., Besenfelder, U., Vogl, C., Brem, G., & Mayrhofer, C. (2019) · PROTEOMICS · doi:10.1002/pmic.201800319 · Cited by 18

Non-canonical functions of autophagy proteins in immunity and infection

Münz, C. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.100987 · Cited by 18

Biogenesis of JC polyomavirus associated extracellular vesicles

Morris‐Love, J., O’Hara, B. A., Gee, G. V., Dugan, A. S., O’Rourke, R., Armstead, B. E., Assetta, B., Haley, S. A., & Atwood, W. J. (2022) · Journal of Extracellular Biology · doi:10.1002/jex2.43 · Cited by 16

The autophagy-senescence axis as a threshold model of aging and therapeutic targeting

Bahar, M. E., Hwang, J. S., Lai, T. H., Akter, K.-M., Maulidi, R. F., & Kim, D. R. (2026) · Redox Biology · doi:10.1016/j.redox.2026.104079 · Cited by 20

Vibrio cholerae cytotoxin MakA induces noncanonical autophagy resulting in the spatial inhibition of canonical autophagy

Corkery, D., Nadeem, A., Aung, K. M., Hassan, A., Liu, T., Cervantes-Rivera, R., Lystad, A. H., Wang, H., Persson, K., Puhar, A., et al. (2020) · Journal of Cell Science · doi:10.1242/jcs.252015 · Cited by 16

Post-Transcriptional Control of mRNA Metabolism and Protein Secretion: The Third Level of Regulation within the NF-κB System

Priester, J., Dreute, J., Kracht, M., & Schmitz, M. L. (2022) · Biomedicines · doi:10.3390/biomedicines10092108 · Cited by 19

Ghost messages: cell death signals spread

Zhang, M., Lin, Y., Chen, R., Yu, H., Li, Y., Chen, M., Dou, C., Yin, P., Zhang, L., & Tang, P. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-01004-0 · Cited by 18

Roles for Autophagy Proteins in Immunity and Host Defense

Kinsella, R. L., Nehls, E. M., & Stallings, C. L. (2018) · Veterinary Pathology · doi:10.1177/0300985818754967 · Cited by 18

Autophagy mediates the secretion of macrophage migration inhibitory factor from cardiomyocytes upon serum-starvation

Wu, J., Deng, X., Gao, J., Gao, W. D., Xiao, H., Wang, X., & Zhang, Y. (2019) · Science China Life Sciences · doi:10.1007/s11427-019-9567-1 · Cited by 17

A switch from lysosomal degradation to secretory autophagy initiates osteogenic bone metastasis in prostate cancer

Wei, X., Liang, M., Deng, M., Zheng, J., Luo, F., & Ma, Q. (2024) · Journal of Extracellular Vesicles · doi:10.1002/jev2.70002 · Cited by 15

Autophagy Pathways in CNS Myeloid Cell Immune Functions

Keller, C. W., Münz, C., & Lünemann, J. D. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.09.003 · Cited by 17

Lysosomal cathepsins act in concert with Gasdermin-D during NAIP/NLRC4-dependent IL-1β secretion

Branco, L. M., Amaral, M. P., Boekhoff, H., de Lima, A. B. F., de Farias, I. S., Lage, S. L., Pereira, G. J. S., Franklin, B. S., & Bortoluci, K. R. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05476-3 · Cited by 16

Autophagy in Inflammatory Response against SARS-CoV-2

Resnik, R., Mingorance, F. L., Rivera, F., Mitchell, F., González, C. D., & Vaccaro, M. I. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054928 · Cited by 17

The role of interleukin -1 family in fibrotic diseases

Wang, H., Wu, J., Li, M., Bai, Y., & Liu, J. (2023) · Cytokine · doi:10.1016/j.cyto.2023.156161 · Cited by 16

Distinct surveillance pathway for immunopathology during acute infection via autophagy and SR-BI

Pfeiler, S., Khandagale, A. B., Magenau, A., Nichols, M., Heijnen, H. F. G., Rinninger, F., Ziegler, T., Seveau, S. M., Schubert, S., Zahler, S., et al. (2016) · Scientific Reports · doi:10.1038/srep34440 · Cited by 18

The flavonoids of Sophora flavescens exerts anti-inflammatory activity via promoting autophagy of Bacillus Calmette-Guérin-stimulated macrophages

Kan, L. L., Liu, D., Chan, B. C.-L., Tsang, M. S., Hou, T., Leung, P., Lam, C. W.-K., & Wong, C. K. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ma0720-682rr · Cited by 16

IIIM-941, a Stilbene Derivative Inhibits NLRP3 Inflammasome Activation by Inducing Autophagy

Ali, M., Gupta, M., Wani, A., Sharma, A., Abdullaha, M., Kour, D., Choudhary, S., Bharate, S. B., Singh, G., & Kumar, A. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.695712 · Cited by 16

Maintaining Golgi Homeostasis: A Balancing Act of Two Proteolytic Pathways

Benyair, R., Eisenberg‐Lerner, A., & Merbl, Y. (2022) · Cells · doi:10.3390/cells11050780 · Cited by 16

Mycobacterium tuberculosisRv1265 promotes mycobacterial intracellular survival and alters cytokine profile of the infected macrophage

Luo, H., Zeng, J., Huang, Q., Liu, M., Abdalla, A. E., Xie, L., Wang, H., & Xie, J. (2015) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2015.1046935 · Cited by 15

Sec16 in conventional and unconventional exocytosis: Working at the interface of membrane traffic and secretory autophagy?

Tang, B. L. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25842 · Cited by 15

GRASP55: A Multifunctional Protein

Wu, H., Li, T., & Zhao, J. (2020) · Current Protein and Peptide Science · doi:10.2174/1389203721666200218105302 · Cited by 16

An unconventional autophagic pathway that inhibits ATP secretion during apoptotic cell death

Terraza-Silvestre, E., Villamuera, R., Bandera-Linero, J., Letek, M., Oña-Sánchez, D., Ramón-Barros, C., Moyano-Jimeno, C., & Pimentel‐Muiños, F. X. (2025) · Nature Communications · doi:10.1038/s41467-025-58619-3 · Cited by 18

Autophagy-independent role of ATG9A vesicles as carriers for galectin-9 secretion

Zhang, W., Ji, C., Li, X., He, T., Jiang, W., Liu, Y., Wu, M., Zhao, Y., Chen, X., Wang, X., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-59605-5 · Cited by 16

Extracellular Vesicles in the Crosstalk of Autophagy and Apoptosis: A Role for Lipid Rafts

Longo, A., Manganelli, V., Misasi, R., Riitano, G., Çağlar, T. R., Fasciolo, E., Recalchi, S., Sorice, M., & Garofalo, T. (2025) · Cells · doi:10.3390/cells14100749 · Cited by 15

Selective Secretion of KDEL-Bearing Proteins: Mechanisms and Functions

Palazzo, F. C., Sitia, R., & Tempio, T. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.967875 · Cited by 15

Perspectives of autophagy-tethering compounds (ATTECs) in drug discovery

Ding, Y., Xing, D., Fei, Y., Luo, S., & Lu, B. (2024) · Medicine Plus · doi:10.1016/j.medp.2023.100004 · Cited by 16

Autophagy: a necessary evil in cancer and inflammation

Mathur, A., Ritu, R., Chandra, P., & Das, A. (2024) · 3 Biotech · doi:10.1007/s13205-023-03864-w · Cited by 16

ESCRT-III: a versatile membrane remodeling machinery and its implications in cellular processes and diseases

Park, J., Kim, J., Park, H., Kim, T., & Lee, S. (2024) · Animal Cells and Systems · doi:10.1080/19768354.2024.2380294 · Cited by 18

Canonical and noncanonical autophagy: involvement in Parkinson’s disease

Sakurai, M., & Kuwahara, T. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1518991 · Cited by 16

Mapping autophagosome contents identifies interleukin-7 receptor-α as a key cargo modulating CD4+ T cell proliferation

Zhou, D., Borsa, M., Puleston, D. J., Zellner, S., Capera, J., Sanderson, S., Schifferer, M., Hester, S. S., Ge, X., Fischer, R., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-32718-x · Cited by 15

Rab-dependent cellular trafficking and amyotrophic lateral sclerosis

Parakh, S., Perri, E. R., Jagaraj, C. J., Ragagnin, A., & Atkin, J. D. (2018) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2018.1553926 · Cited by 15

The novel interplay between CD44 standard isoform and the caspase-1/IL1B pathway to induce hepatocellular carcinoma progression

Li, J., Zhang, Y., Ruan, R., He, W., & Qian, Y. (2020) · Cell Death and Disease · doi:10.1038/s41419-020-03158-6 · Cited by 18

Degradative and Non-Degradative Roles of Autophagy Proteins in Metabolism and Metabolic Diseases

Kuramoto, K., & He, C. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.844481 · Cited by 16

Japanese Flounder HMGB1: A DAMP Molecule That Promotes Antimicrobial Immunity by Interacting with Immune Cells and Bacterial Pathogen

Chen, Y., Yu, C., Jiang, S., & Sun, L. (2022) · Genes · doi:10.3390/genes13091509 · Cited by 14

Role of adiponectin in osteoarthritis

Feng, X., Xiao, J., & Bai, L. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.992764 · Cited by 15

Non-canonical autophagy in aging and age-related diseases

Kumar, A. V., & Mills, J. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1137870 · Cited by 15

Early signs of neurodegenerative diseases: Possible mechanisms and targets for Golgi stress

Liu, M., Duan, Y., Dong, J., Zhang, K., Jin, X., Gao, M., Jia, H., Chen, J., Liu, M., Wei, M., et al. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116646 · Cited by 14

Folding of Fibroblast Growth Factor 1 Is Critical for Its Nonclassical Release

Prudovsky, I. A., Kacer, D., Davis, J., Shah, V., Jayanthi, S., Huber, I., Rajalingam, D., Ganter, O., Soldi, R., Neivandt, D. J., et al. (2016) · Biochemistry · doi:10.1021/acs.biochem.5b01341 · Cited by 14

Secretory Autophagosomes from Alveolar Macrophages Exacerbate Acute Respiratory Distress Syndrome by Releasing IL-1β

Xu, X., Liu, X., Dong, X., Qiu, H., Yang, Y., & Liu, L. (2022) · Journal of Inflammation Research · doi:10.2147/jir.s344857 · Cited by 14

Crosstalk between exosomes and autophagy in spinal cord injury: fresh positive target for therapeutic application

Li, R., Hu, Q., Shi, X., Luo, Z., & Dong-hua, S. (2022) · Cell and Tissue Research · doi:10.1007/s00441-022-03699-6 · Cited by 15

Secretory autophagy: a turn key for understanding AMD pathology and developing new therapeutic targets?

Błasiak, J., & Kaarniranta, K. (2022) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2022.2157260 · Cited by 16

Identification of Proteins Interacting with Cytoplasmic High-Mobility Group Box 1 during the Hepatocellular Response to Ischemia Reperfusion Injury

Zhang, T., Wei, W., Dirsch, O., Krüger, T., Kan, C., Xie, C., Kniemeyer, O., Fang, H., Settmacher, U., & Dahmen, U. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18010167 · Cited by 14

TMEDs mediate versatile cargo transport in vesicle-dependent unconventional secretion

Zheng, J., Wang, H., Sun, Y., Chang, P., Deng, X., Zhang, L., Zhu, L., Zhu, K., Peng, D., Deng, H., et al. (2025) · The Journal of Cell Biology · doi:10.1083/jcb.202503075 · Cited by 13

Resurrecting Golgi proteins to grasp Golgi ribbon formation and self-association under stress

Mendes, L. F. S., Batista, M. R. B., Kava, E., Bleicher, L., Micheletto, M. C., & Costa-Filho, A. J. (2022) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2021.11.173 · Cited by 13

Evasion of oncogene-induced senescence by gammaherpesviruses

Leidal, A. M., Pringle, E. S., & McCormick, C. (2012) · Current Opinion in Virology · doi:10.1016/j.coviro.2012.09.009 · Cited by 13

Tp47 induces cell death involving autophagy and mTOR in human microglial HMO6 cells

Liu, W.-N., Jiang, X., JunRen, Zhuang, J., Chen, M., Zhu, S.-G., Yang, T., Yan, J., & Liu, L. (2019) · International Immunopharmacology · doi:10.1016/j.intimp.2019.04.013 · Cited by 13

Unconventional secretion: cargo channeling by TMED10

Nguyen, T. A., & Debnath, J. (2020) · Cell Research · doi:10.1038/s41422-020-0382-x · Cited by 13

Rab8 Promotes Mutant HTT Aggregation, Reduces Neurodegeneration, and Ameliorates Behavioural Alterations in a Drosophila Model of Huntington’s Disease

Delfino, L., Mason, R. P., Kyriacou, C. P., Giorgini, F., & Rosato, E. (2020) · Journal of Huntington s Disease · doi:10.3233/jhd-200411 · Cited by 13

Autophagy and Extracellular Vesicles in Colorectal Cancer: Interactions and Common Actors?

Auger, C., Christou, N., Brunel, A., Perraud, A., & Verdier, M. (2021) · Cancers · doi:10.3390/cancers13051039 · Cited by 14

To be or not to be cell autonomous? Autophagy says both

Fenouille, N., Nascimbeni, A. C., Botti, J., Dupont, N., Morel, É., & Codogno, P. (2017) · Essays in Biochemistry · doi:10.1042/ebc20170025 · Cited by 15

Autophagy induced by avian reovirus enhances viral replication in chickens at the early stage of infection

Niu, X., Zhang, C., Wang, Y., Guo, M., Ruan, B., Wang, X., Wu, T., Zhang, X., & Wu, Y. (2019) · BMC Veterinary Research · doi:10.1186/s12917-019-1926-5 · Cited by 13

No evidence for cell‐to‐cell transmission of the unfolded protein response in cell culture

van Ziel, A. M., Wolzak, K., Nölle, A., Hoetjes, P. J., Berenjeno‐Correa, E., van Anken, E., Struys, E. A., & Scheper, W. (2019) · Journal of Neurochemistry · doi:10.1111/jnc.14856 · Cited by 13

Klotho-mediated changes in the expression of Atg13 alter formation of ULK1 complex and thus initiation of ER- and Golgi-stress response mediated autophagy

Mytych, J., Sołek, P., Będzińska, A., Rusinek, K., Warzybok, A., Tabęcka-Łonczyńska, A., & Koziorowski, M. (2019) · APOPTOSIS · doi:10.1007/s10495-019-01579-z · Cited by 13

Molecular and subcellular mechanisms of vital macrophage extracellular trap formation

Lee, Y., Brenner, M., Aziz, M., & Wang, P. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1608428 · Cited by 13

GRASP55 restricts early-stage autophagy and regulates spatial organization of the early secretory network

Liu, J. Y., Lin, Y.-H. T., Leidal, A. M., Huang, H. H., Ye, J., Wiita, A. P., & Debnath, J. (2021) · Biology Open · doi:10.1242/bio.058736 · Cited by 12

Desferrioxamine Ameliorates Lipopolysaccharide-Induced Lipocalin-2 Upregulation via Autophagy Activation in Primary Astrocytes

Cui, J., Yu, Y., Wang, J., Song, N., & Xie, J. (2022) · Molecular Neurobiology · doi:10.1007/s12035-021-02687-1 · Cited by 12

Atg8/LC3 controls systemic nutrient surplus signaling in flies and humans

Madan, A., Kelly, K., Bahk, P., Sullivan, C. E., Poling, M. E., Brent, A. E., Alassaf, M., Dubrulle, J., & Rajan, A. (2024) · Current Biology · doi:10.1016/j.cub.2024.06.005 · Cited by 12

Unconventional secretion of PARK7 requires lysosomal delivery via chaperone-mediated autophagy and specialized SNARE complex

Dash, B. K., Urano, Y., Mita, Y., Ashida, Y., Hirose, R., & Noguchi, N. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2414790122 · Cited by 12

Up-regulation of the active form of small GTPase Rab13 promotes macroautophagy in vascular endothelial cells

Zhang, L., Dai, F., Cui, L., Zhou, B., & Guo, Y. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2017.01.003 · Cited by 12

Role of Autophagy in Von Willebrand Factor Secretion by Endothelial Cells and in the In Vivo Thrombin-Antithrombin Complex Formation Promoted by the HIV-1 Matrix Protein p17

Bugatti, A., Marsico, S., Mazzuca, P., Schulze, K., Ebensen, T., Giagulli, C., Peña, E., Badimón, L., SLEVIN, M. A., Caruso, A., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21062022 · Cited by 12

Diverse cellular strategies for the export of leaderless proteins

Zheng, J., & Ge, L. (2022) · National Science Open · doi:10.1360/nso/20220018 · Cited by 12

Domain architecture of vasohibins required for their chaperone‐dependent unconventional extracellular release

Kadonosono, T., Yimchuen, W., tsubaki, T., Shiozawa, T., Suzuki, Y., Kuchimaru, T., Sato, Y., & Kizaka‐Kondoh, S. (2016) · Protein Science · doi:10.1002/pro.3089 · Cited by 12

Optimized protocols for studying the NLRP3 inflammasome and assessment of potential targets of CP-453,773 in undifferentiated THP1 cells

Guzova, J. A., Primiano, M. J., Jiao, A., Stock, J. L., Lee, C., Winkler, A. R., & Hall, J. P. (2019) · Journal of Immunological Methods · doi:10.1016/j.jim.2019.02.002 · Cited by 12

Autophagy and Bacterial infections

Cadwell, K., Abraham, C., Bel, S., Chauhan, S., Coers, J., Colombo, M. I., Davis, J. R., Hofius, D., Nguyen, H. T. T., Ogawa, M., et al. (2025) · Autophagy Reports · doi:10.1080/27694127.2025.2542904 · Cited by 12

Enhancing Immunogenicity in Metastatic Melanoma: Adjuvant Therapies to Promote the Anti-Tumor Immune Response

Pelka, S., & Guha, C. (2023) · Biomedicines · doi:10.3390/biomedicines11082245 · Cited by 11

The molecular mechanism of MiR-26a-5p regulates autophagy and activates NLRP3 inflammasome to mediate cardiomyocyte hypertrophy

Tang, L., Wang, W., Tang, Q.-F., & Wang, L. (2024) · BMC Cardiovascular Disorders · doi:10.1186/s12872-023-03695-w · Cited by 11

Autophagy Promotes Enrichment of Raft Components within Extracellular Vesicles Secreted by Human 2FTGH Cells

Manganelli, V., Dini, L., Tacconi, S., Dinarelli, S., Capozzi, A., Riitano, G., Recalchi, S., Çağlar, T. R., Fratini, F., Misasi, R., et al. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25116175 · Cited by 11

Role of canonical and noncanonical autophagy pathways in shaping the life journey of B cells

Wang, Y., Wu, L., & Kaer, L. V. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1426204 · Cited by 13

Presenilins as hub proteins controlling the endocytic and autophagic pathways and small extracellular vesicle secretion

Lauritzen, I., Bini, A., Bécot, A., Gay, A.-S., Badot, C., Pagnotta, S., Chami, M., & Checler, F. (2025) · Journal of Extracellular Vesicles · doi:10.1002/jev2.70019 · Cited by 12

In situ architecture of the intercellular organelle reservoir between epididymal epithelial cells by volume electron microscopy

Li, X., Qiao, F., Guo, J., Jiang, T., Lou, H., Li, H., Xie, G., Wu, H., Wang, W., Pei, R., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56807-9 · Cited by 11

Dexmedetomidine protects against high mobility group box 1‐induced cellular injury by inhibiting pyroptosis

Ji, X., Guo, Y., Zhou, G., Wang, Y., Zhang, J., Wang, Z., & Wang, Q. (2019) · Cell Biology International · doi:10.1002/cbin.11140 · Cited by 11

Secretory Autophagosomes from Alveolar Macrophages Exacerbate Acute Respiratory Distress Syndrome by Releasing IL-1β

Xu, X., Liu, X., Dong, X., Qiu, H., Yang, Y., & Liu, L. (2022) · Dove Medical Press (Taylor and Francis Group) · Cited by 11

Coordination of RAB-8 and RAB-11 during unconventional protein secretion

Li, X., Liu, B., Wen, Y., Wang, J., Guo, Y. R., Shi, A., & Lin, L. (2023) · The Journal of Cell Biology · doi:10.1083/jcb.202306107 · Cited by 11

Cellular repressor of E1A-stimulated genes inhibits inflammation to decrease atherosclerosis in ApoE−/− mice

Sun, M., Tian, X., Liu, Y., Zhu, N., Yang, L., Yang, G., Peng, C., Yan, C., & Han, Y. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.07.001 · Cited by 11

Role of Alarmins in the Pathogenesis of Systemic Sclerosis

Giovannetti, A., Straface, E., Rosato, E., Casciaro, M., Pioggia, G., & Gangemi, S. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21144985 · Cited by 12

Host Cell Signatures of the Envelopment Site within Beta-Herpes Virions

Lučin, H. M., Zagorac, G. B., Marcelić, M., & Lučin, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23179994 · Cited by 11

Autophagy and Crohn’s Disease

Nys, K., Vermeire, S., & Agostinis, P. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-405530-8.00005-4 · Cited by 11

Disulfide bridge-dependent dimerization triggers FGF2 membrane translocation into the extracellular space

Lolicato, F., Steringer, J. P., Saleppico, R., Beyer, D., Fernandez-Sobaberas, J., Unger, S., Klein, S., Riegerová, P., Wegehingel, S., Müller, H.-M., et al. (2024) · eLife · doi:10.7554/elife.88579 · Cited by 9

Alzheimer's disease-associated mutant ubiquitin (UBB+1) is secreted through an autophagosome-like vesicle-mediated unconventional pathway

Wagh, A. R., Sulakshane, P., & Glickman, M. H. (2023) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2023.194936 · Cited by 11

Klotho-beta attenuates Rab8a-mediated exosome regulation and promotes prostate cancer progression

Wu, T., Zhang, Y., Han, Q., Lü, X., Cheng, Y., Chen, J., Sha, J., & Xia, W. (2023) · Oncogene · doi:10.1038/s41388-023-02807-2 · Cited by 10

Picornavirus security proteins promote the release of extracellular vesicle enclosed viruses via the modulation of host kinases

Defourny, K. A. Y., Pei, X., van Kuppeveld, F. J. M., & Hoen, E. N. M. N. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012133 · Cited by 10

Potential of autophagy in subretinal fibrosis in neovascular age-related macular degeneration

Błasiak, J., Pawłowska, E., Heloterä, H., Йонов, М., Derwich, M., & Kaarniranta, K. (2025) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00732-8 · Cited by 10

Nonclassically Secreted Regulators of Angiogenesis

Prudovsky, I. A. (2013) · Angiology Open Access · doi:10.4172/2329-9495.1000101 · Cited by 11

Induction of Autophagy to Achieve a Human Immunodeficiency Virus Type 1 Cure

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