Reversible suppression of autophagy in a mouse model reveals neuronal resilience

T Tomoya Eguchi (Department of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, The University of Tokyo, Tokyo, Japan.) M Manabu Abe (Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.) T Takuya Tomita (Division of Protein Metabolism, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.) H Hideaki Morishita (Department of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, The University of Tokyo, Tokyo, Japan.) Y Yasushi Saeki (Division of Protein Metabolism, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.) K Kenji Sakimura (Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.) K Kenji F. Tanaka (Division of Brain Sciences, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.) N Noboru Mizushima

Abstract

Impairments in intracellular quality-control mechanisms, including autophagy, affect neuronal integrity and function. Despite numerous studies aimed at slowing neuronal deterioration, it remains unclear whether neuronal function and intracellular quality can be restored once impaired. We developed a mouse model in which autophagy could be rapidly and reversibly regulated to investigate the reversibility of such defects. Suppressing autophagy led to proteome and transcriptome changes, inclusion body accumulation, and axonal swelling, all of which were largely ameliorated after autophagy restoration. Consistent with these cellular abnormalities, autophagy suppression induced motor and cognitive dysfunction, which was also reversed on autophagy restoration. Our findings elucidate the potential resilience of neuronal function and quality enabled by intracellular clearance.

Article Details

Journal Science
Volume / Issue Vol. 392, Issue 6805
Published June 25, 2026
Pages 1363-1368
ISSN 0036-8075
Publisher American Association for the Advancement of Science

Journal Info

Science

American Association for the Advancement of Science

ISSN: 0036-8075 Social Sciences

Authors (8)

T

Tomoya Eguchi

Department of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

M

Manabu Abe

Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.

T

Takuya Tomita

Division of Protein Metabolism, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

H

Hideaki Morishita

Department of Biochemistry and Molecular Biology, Graduate School and Faculty of Medicine, The University of Tokyo, Tokyo, Japan.

Y

Yasushi Saeki

Division of Protein Metabolism, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

K

Kenji Sakimura

Department of Cellular Neurobiology, Brain Research Institute, Niigata University, Niigata, Japan.

K

Kenji F. Tanaka

Division of Brain Sciences, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo, Japan.

N

Noboru Mizushima