Sakai, Y., Behrends, C., Cuervo, A. M., Debnath, J., Izumi, M., Jenny, A., Molinari, M., Nakamura, S., Oku, M., Otegui, M. S., Santambrogio, L., Shen, H.-M., Taguchi, T., Thumm, M., Ushimaru, T., Xie, Z.
& Reggiori, F. (2026).
Microautophagy: definition, classification, and the complexity of the underlying mechanisms.
Autophagy,
22(1), 3-9.
https://doi.org/10.1080/15548627.2025.2559687
Sakai, Y., Behrends, C., Debnath, J., Izumi, M., Jenny, A., Molinari, M., Nakamura, S., Oku, M., Otegui, M. S., Santambrogio, L., Shen, H.-M., Taguchi, T., Thumm, M., Ushimaru, T., Xie, Z., Cuervo, A. M.
& Reggiori, F. (2026).
Microautophagy: current understanding of its molecular mechanisms and functions.
Autophagy Reports,
5(1), Article 2626661.
https://doi.org/10.1080/27694127.2026.2626661
Mauthe, M.
, van de Beek, N., Mari, M., Korsten, G., Nobari, P.
, Castelino, K. B., de Mattos, E. P., Ouhida, I., Dijkstra, J. L., Schipper-Krom, S., de la Ballina, L. R.
, Mueller, M. R., Simonsen, A., Hipp, M. S., Kapitein, L. C., Kampinga, H. H.
& Reggiori, F. (2025).
A chaperone-proteasome-based fragmentation machinery is essential for aggrephagy.
Nature Cell Biology,
27(9), 1448-1464.
https://doi.org/10.1038/s41556-025-01747-1
Javed, R.
, Mari, M., Trosdal, E., Lopes Alberto Duque, T., Paddar, M., Allers, L., Akepati, P., Mudd, M. H.
, Reggiori, F. & Deretic, V. (2025).
ATG9A controls all stages of autophagosome biogenesis.
Autophagy,
21(8), 1859-1861.
https://doi.org/10.1080/15548627.2025.2494802
Javed, R.
, Mari, M., Trosdal, E., Duque, T., Paddar, M. A., Allers, L., Mudd, M. H., Claude-Taupin, A., Akepati, P. R., Hendrix, E., He, Y., Salemi, M., Phinney, B., Uchiyama, Y.
, Reggiori, F. & Deretic, V. (2025).
ATG9A facilitates the closure of mammalian autophagosomes.
The Journal of Cell Biology,
224(2), Article e202404047.
https://doi.org/10.1083/jcb.202404047
Münz, C., Campbell, G. R., Esclatine, A., Faure, M., Labonte, P., Lussignol, M., Orvedahl, A., Altan-Bonnet, N., Bartenschlager, R., Beale, R., Cirone, M., Espert, L., Jung, J., Leib, D.
, Reggiori, F., Sanyal, S., Spector, S. A., Thiel, V., Viret, C. ... Wodrich, H. (2025).
Autophagy machinery as exploited by viruses.
Autophagy Reports,
4(1), Article 2464986.
https://doi.org/10.1080/27694127.2025.2464986
Grumati, P., Morozzi, G., Hölper, S.
, Mari, M., Harwardt, M.-L. I. E., Yan, R., Müller, S.
, Reggiori, F., Heilemann, M. & Dikic, I. (2025).
Correction: Full length RTN3 regulates turnover of tubular endoplasmic reticulum via selective autophagy.
eLife,
14.
https://doi.org/10.7554/eLife.107151
Hu, L., van der Sluis, R. M., Castelino, K. B., Zhang, B.-C., Ronit, A.
, Zillinger, T., Werner, M., Jørgensen, S. E., Hansen, A. L., Pedersen, A., Narita, R., Reinert, L. S., Bundgaard, B., Holm, C. K., Cobat, A., Casanova, J.-L.
, Reggiori, F., Mari, M., Paludan, S. R. ... COVID Human Genetic Effort (2025).
Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2.
Nature Communications,
16(1), Article 10618.
https://doi.org/10.1038/s41467-025-65308-8
Gómez-Sánchez, R., Chumpen Ramirez, S.
, Vargas Duarte, P., Hu, Y., Mari, M., Olschewski, K., Hardenberg, R., Fromme, J. C., Ungermann, C.
& Reggiori, F. (2025).
Establishment of the phagophore-ERES membrane contact site initiates phagophore elongation.
Nature Structural & Molecular Biology,
32(11), 2319-2334.
https://doi.org/10.1038/s41594-025-01621-6
Cong, Y., Verlhac, P.
, Green, B. B., de Vries-Idema, J.
, Strauss, L. M., Río-Bergé, C., Etzerodt, A., Nejsum, L. N., Huckriede, A. L. W.
& Reggiori, F. (2025).
Influenza A virus subverts the LC3-pericentrin dynein adaptor complex for host cytoplasm entry.
Science Advances,
11(24), Article eadu7602.
https://doi.org/10.1126/sciadv.adu7602
Zein, L., Dietrich, M., Balta, D., Bader, V., Scheuer, C., Zellner, S., Weinelt, N., Vandrey, J.
, Mari, M. C., Behrends, C., Zunke, F., Winklhofer, K. F. & Van Wijk, S. J. L. (2025).
Linear ubiquitination at damaged lysosomes induces local NFKB activation and controls cell survival.
Autophagy,
21(5), 1075-1095.
https://doi.org/10.1080/15548627.2024.2443945
Wedman, J. J., de Vries, L., van Lingen, B., van der Zwaag, M., Gómez-Sánchez, R., Hardenberg, R., Huibers, W., Permentier, H., Strauss, E., Chang, M.
, Reggiori, F., de Kroon, A. I., Sibon, O. C. M. & Schepers, H. (2025).
Opt1 imports CoA precursors as glutathione mixed disulfides.
The Journal of Biological Chemistry,
301(9), Article 110503.
https://doi.org/10.1016/j.jbc.2025.110503
Thorup, C. V., Jeppesen, C. N. A., Jensen, T. H., Tinggaard, A. B., Hvas, C. L., Rud, C. L., Skou, M. K.
, Mortensen, J. K., Reggiori, F., Dengjel, J.
, Wang, J., Farup, J., Jessen, N., Kim, W. Y. & Wiggers, H. (2025).
POLYamine treatment in elderly patients with Coronary Artery Disease (POLYCAD): study protocol for a Danish randomised, double-blind, placebo-controlled trial of spermidine treatment versus placebo.
Trials,
26(1), Article 452.
https://doi.org/10.1186/s13063-025-09176-z
Zhang, B.-C., Pedersen, A., Reinert, L. S., Li, Y.
, Narita, R., Idorn, M., Hu, L., Skouboe, M. K., Li, S.
, Maimaitili, M., Ding, X., Cong, Y., Zhao, J., Frémond, M.-L.
, Mikkelsen, K., Gao, Z., Huang, J.-R.
, Thomsen, E. A., Mikkelsen, J. H. ... Paludan, S. R. (2025).
STING signals to NF-κB from late endolysosomal compartments using IRF3 as an adaptor.
Nature Immunology,
26(11), 1916-1930.
https://doi.org/10.1038/s41590-025-02283-8
Filali-Mouncef, Y., Leytens, A., Vargas Duarte, P., Zampieri, M., Dengjel, J.
& Reggiori, F. (2024).
An APEX2-based proximity-dependent biotinylation assay with temporal specificity to study protein interactions during autophagy in the yeast Saccharomyces cerevisiae.
Autophagy,
20(10), 2323-2337.
https://doi.org/10.1080/15548627.2024.2366749