Phagophore Ceramide Promotes <scp>LC3</scp> Lipidation and Autophagy in T‐Lymphoid Cell Death

The bioactive sphingolipid ceramide induces various types of cell death, including autophagy-dependent cell death (ADCD). However, its role in autophagy and ADCD is not fully understood. Here, we demonstrated that amino acid deprivation (AA[-]) in murine lymphoid WR19L cells promoted the accumulation of ceramide at phagophores and autophagy, resulting in ADCD. Control of ceramide production by sphingomyelin synthase 1 and neutral sphingomyelinase 2 altered cell fate by regulating AA(-)-induced autophagy and ADCD. In vitro reconstruction analysis of phosphatidylethanolamine (PE) binding to microtubule-associated protein-1 light chain-3 (LC3), a key step in phagophore formation leading to autophagic flux, revealed that ceramide promoted the PE lipidation of LC3. These results suggest that ceramide promotes autophagosome formation by enhancing PE lipidation of LC3, leading to excess autophagy and ADCD. This study highlights novel insights into the ceramide/sphingomyelin balance at autophagy-related membranes, which controls the switch on autophagy and ADCD through enhanced lipidation of LC3.

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Publication Details

Journal
The FASEB Journal
Published
2025-05-26
DOI
https://doi.org/10.1096/fj.202500348r
Citations
2
Primary Topic
Sphingolipid Metabolism and Signaling
Type
article
Field-Weighted Citation Impact
1.61

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article

Phagophore Ceramide Promotes LC3 Lipidation and Autophagy in T‐Lymphoid Cell Death

Hiromi Kirisako, Shingo Nagaya, Yoshinori Ohsumi, Hitoshi Nakatogawa et al.
2 citations
The FASEB Journal
Sphingolipid Metabolism and Signaling
1.61
article

Phagophore Ceramide Promotes LC3 Lipidation and Autophagy in T‐Lymphoid Cell Death

Hiromi Kirisako, Shingo Nagaya, Yoshinori Ohsumi, Hitoshi Nakatogawa, Makoto Taniguchi, Toshiro Okazaki
article en
2 citations

Abstract

The bioactive sphingolipid ceramide induces various types of cell death, including autophagy-dependent cell death (ADCD). However, its role in autophagy and ADCD is not fully understood. Here, we demonstrated that amino acid deprivation (AA[-]) in murine lymphoid WR19L cells promoted the accumulation of ceramide at phagophores and autophagy, resulting in ADCD. Control of ceramide production by sphingomyelin synthase 1 and neutral sphingomyelinase 2 altered cell fate by regulating AA(-)-induced autophagy and ADCD. In vitro reconstruction analysis of phosphatidylethanolamine (PE) binding to microtubule-associated protein-1 light chain-3 (LC3), a key step in phagophore formation leading to autophagic flux, revealed that ceramide promoted the PE lipidation of LC3. These results suggest that ceramide promotes autophagosome formation by enhancing PE lipidation of LC3, leading to excess autophagy and ADCD. This study highlights novel insights into the ceramide/sphingomyelin balance at autophagy-related membranes, which controls the switch on autophagy and ADCD through enhanced lipidation of LC3.

The FASEB JournalVol. 39(11)
Tokyo Institute of Technology (JP), Kanazawa Medical University (JP), Ishikawa Prefectural University (JP), University of Yamanashi (JP)
Takeda Science Foundation, Ministry of Education, Culture, Sports, Science and Technology, Kanazawa Medical University, Japan Society for the Promotion of Science
Openalex Percentile: Top 17%
Sphingolipid Metabolism and Signaling
1.61
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Phagophore Ceramide Promotes <scp>LC3</scp> Lipidation and Autophagy in T‐Lymphoid Cell Death — Hiromi Kirisako, Shingo Nagaya, et al. · The FASEB Journal (2025) | TGRS Research Map | TGRS