Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]

Publication Date:
2018-03-06
Publisher:
The Company of Biologists
Print ISSN:
0950-1991
Electronic ISSN:
1477-9129
Topics:
Biology
Published by:
_version_ 1836398818366586880
autor Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
beschreibung Takayuki Tatsumi, Kaori Takayama, Shunsuke Ishii, Atsushi Yamamoto, Taichi Hara, Naojiro Minami, Naoyuki Miyasaka, Toshiro Kubota, Akira Matsuura, Eisuke Itakura, and Satoshi Tsukamoto Although autophagy is classically viewed as a non-selective degradation system, recent studies have revealed that various forms of selective autophagy also play crucial physiological roles. However, the induction of selective autophagy is not well understood. In this study, we established a forced selective autophagy system using a fusion of an autophagy adaptor and a substrate-binding protein. In both mammalian cells and fertilized mouse embryos, efficient forced lipophagy was induced by expression of a fusion of p62 (Sqstm1) and a lipid droplet (LD)-binding domain. In mouse embryos, induction of forced lipophagy caused a reduction in LD size and number, and decreased the triglyceride level throughout embryonic development, resulting in developmental retardation. Furthermore, lipophagy-induced embryos could eliminate excess LDs and were tolerant of lipotoxicity. Thus, by inducing forced lipophagy, expression of the p62 fusion protein generated LD-depleted cells, revealing an unexpected role of LD during preimplantation development.
citation_standardnr 6183466
datenlieferant ipn_articles
feed_id 1748
feed_publisher The Company of Biologists
feed_publisher_url http://www.biologists.com/
insertion_date 2018-03-06
journaleissn 1477-9129
journalissn 0950-1991
publikationsjahr_anzeige 2018
publikationsjahr_facette 2018
publikationsjahr_intervall 7984:2015-2019
publikationsjahr_sort 2018
publisher The Company of Biologists
quelle Development
relation http://dev.biologists.org/cgi/content/short/145/4/dev161893?rss=1
search_space articles
shingle_author_1 Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
shingle_author_2 Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
shingle_author_3 Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
shingle_author_4 Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
shingle_catch_all_1 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
Takayuki Tatsumi, Kaori Takayama, Shunsuke Ishii, Atsushi Yamamoto, Taichi Hara, Naojiro Minami, Naoyuki Miyasaka, Toshiro Kubota, Akira Matsuura, Eisuke Itakura, and Satoshi Tsukamoto Although autophagy is classically viewed as a non-selective degradation system, recent studies have revealed that various forms of selective autophagy also play crucial physiological roles. However, the induction of selective autophagy is not well understood. In this study, we established a forced selective autophagy system using a fusion of an autophagy adaptor and a substrate-binding protein. In both mammalian cells and fertilized mouse embryos, efficient forced lipophagy was induced by expression of a fusion of p62 (Sqstm1) and a lipid droplet (LD)-binding domain. In mouse embryos, induction of forced lipophagy caused a reduction in LD size and number, and decreased the triglyceride level throughout embryonic development, resulting in developmental retardation. Furthermore, lipophagy-induced embryos could eliminate excess LDs and were tolerant of lipotoxicity. Thus, by inducing forced lipophagy, expression of the p62 fusion protein generated LD-depleted cells, revealing an unexpected role of LD during preimplantation development.
Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
The Company of Biologists
0950-1991
09501991
1477-9129
14779129
shingle_catch_all_2 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
Takayuki Tatsumi, Kaori Takayama, Shunsuke Ishii, Atsushi Yamamoto, Taichi Hara, Naojiro Minami, Naoyuki Miyasaka, Toshiro Kubota, Akira Matsuura, Eisuke Itakura, and Satoshi Tsukamoto Although autophagy is classically viewed as a non-selective degradation system, recent studies have revealed that various forms of selective autophagy also play crucial physiological roles. However, the induction of selective autophagy is not well understood. In this study, we established a forced selective autophagy system using a fusion of an autophagy adaptor and a substrate-binding protein. In both mammalian cells and fertilized mouse embryos, efficient forced lipophagy was induced by expression of a fusion of p62 (Sqstm1) and a lipid droplet (LD)-binding domain. In mouse embryos, induction of forced lipophagy caused a reduction in LD size and number, and decreased the triglyceride level throughout embryonic development, resulting in developmental retardation. Furthermore, lipophagy-induced embryos could eliminate excess LDs and were tolerant of lipotoxicity. Thus, by inducing forced lipophagy, expression of the p62 fusion protein generated LD-depleted cells, revealing an unexpected role of LD during preimplantation development.
Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
The Company of Biologists
0950-1991
09501991
1477-9129
14779129
shingle_catch_all_3 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
Takayuki Tatsumi, Kaori Takayama, Shunsuke Ishii, Atsushi Yamamoto, Taichi Hara, Naojiro Minami, Naoyuki Miyasaka, Toshiro Kubota, Akira Matsuura, Eisuke Itakura, and Satoshi Tsukamoto Although autophagy is classically viewed as a non-selective degradation system, recent studies have revealed that various forms of selective autophagy also play crucial physiological roles. However, the induction of selective autophagy is not well understood. In this study, we established a forced selective autophagy system using a fusion of an autophagy adaptor and a substrate-binding protein. In both mammalian cells and fertilized mouse embryos, efficient forced lipophagy was induced by expression of a fusion of p62 (Sqstm1) and a lipid droplet (LD)-binding domain. In mouse embryos, induction of forced lipophagy caused a reduction in LD size and number, and decreased the triglyceride level throughout embryonic development, resulting in developmental retardation. Furthermore, lipophagy-induced embryos could eliminate excess LDs and were tolerant of lipotoxicity. Thus, by inducing forced lipophagy, expression of the p62 fusion protein generated LD-depleted cells, revealing an unexpected role of LD during preimplantation development.
Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
The Company of Biologists
0950-1991
09501991
1477-9129
14779129
shingle_catch_all_4 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
Takayuki Tatsumi, Kaori Takayama, Shunsuke Ishii, Atsushi Yamamoto, Taichi Hara, Naojiro Minami, Naoyuki Miyasaka, Toshiro Kubota, Akira Matsuura, Eisuke Itakura, and Satoshi Tsukamoto Although autophagy is classically viewed as a non-selective degradation system, recent studies have revealed that various forms of selective autophagy also play crucial physiological roles. However, the induction of selective autophagy is not well understood. In this study, we established a forced selective autophagy system using a fusion of an autophagy adaptor and a substrate-binding protein. In both mammalian cells and fertilized mouse embryos, efficient forced lipophagy was induced by expression of a fusion of p62 (Sqstm1) and a lipid droplet (LD)-binding domain. In mouse embryos, induction of forced lipophagy caused a reduction in LD size and number, and decreased the triglyceride level throughout embryonic development, resulting in developmental retardation. Furthermore, lipophagy-induced embryos could eliminate excess LDs and were tolerant of lipotoxicity. Thus, by inducing forced lipophagy, expression of the p62 fusion protein generated LD-depleted cells, revealing an unexpected role of LD during preimplantation development.
Tatsumi, T., Takayama, K., Ishii, S., Yamamoto, A., Hara, T., Minami, N., Miyasaka, N., Kubota, T., Matsuura, A., Itakura, E., Tsukamoto, S.
The Company of Biologists
0950-1991
09501991
1477-9129
14779129
shingle_title_1 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
shingle_title_2 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
shingle_title_3 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
shingle_title_4 Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
timestamp 2025-06-30T23:33:07.637Z
titel Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
titel_suche Forced lipophagy reveals that lipid droplets are required for early embryonic development in mouse [RESEARCH ARTICLE]
topic W
uid ipn_articles_6183466