Cargando…

Autophagosome formation in relation to the endoplasmic reticulum

Autophagy is a process in which a myriad membrane structures called autophagosomes are formed de novo in a single cell, which deliver the engulfed substrates into lysosomes for degradation. The size of the autophagosomes is relatively uniform in non-selective autophagy and variable in selective auto...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamamoto, Yo-hei, Noda, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579975/
https://www.ncbi.nlm.nih.gov/pubmed/33087127
http://dx.doi.org/10.1186/s12929-020-00691-6
_version_ 1783598703100035072
author Yamamoto, Yo-hei
Noda, Takeshi
author_facet Yamamoto, Yo-hei
Noda, Takeshi
author_sort Yamamoto, Yo-hei
collection PubMed
description Autophagy is a process in which a myriad membrane structures called autophagosomes are formed de novo in a single cell, which deliver the engulfed substrates into lysosomes for degradation. The size of the autophagosomes is relatively uniform in non-selective autophagy and variable in selective autophagy. It has been recently established that autophagosome formation occurs near the endoplasmic reticulum (ER). In this review, we have discussed recent advances in the relationship between autophagosome formation and endoplasmic reticulum. Autophagosome formation occurs near the ER subdomain enriched with phospholipid synthesizing enzymes like phosphatidylinositol synthase (PIS)/CDP-diacylglycerol-inositol 3-phosphatidyltransferase (CDIPT) and choline/ethanolamine phosphotransferase 1 (CEPT1). Autophagy-related protein 2 (Atg2), which is involved in autophagosome formation has a lipid transfer capacity and is proposed to directly transfer the lipid molecules from the ER to form autophagosomes. Vacuole membrane protein 1 (VMP1) and transmembrane protein 41b (TMEM41b) are ER membrane proteins that are associated with the formation of the subdomain. Recently, we have reported that an uncharacterized ER membrane protein possessing the DNAJ domain, called ERdj8/DNAJC16, is associated with the regulation of the size of autophagosomes. The localization of ERdj8/DNAJC16 partially overlaps with the PIS-enriched ER subdomain, thereby implying its association with autophagosome size determination.
format Online
Article
Text
id pubmed-7579975
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-75799752020-10-22 Autophagosome formation in relation to the endoplasmic reticulum Yamamoto, Yo-hei Noda, Takeshi J Biomed Sci Review Autophagy is a process in which a myriad membrane structures called autophagosomes are formed de novo in a single cell, which deliver the engulfed substrates into lysosomes for degradation. The size of the autophagosomes is relatively uniform in non-selective autophagy and variable in selective autophagy. It has been recently established that autophagosome formation occurs near the endoplasmic reticulum (ER). In this review, we have discussed recent advances in the relationship between autophagosome formation and endoplasmic reticulum. Autophagosome formation occurs near the ER subdomain enriched with phospholipid synthesizing enzymes like phosphatidylinositol synthase (PIS)/CDP-diacylglycerol-inositol 3-phosphatidyltransferase (CDIPT) and choline/ethanolamine phosphotransferase 1 (CEPT1). Autophagy-related protein 2 (Atg2), which is involved in autophagosome formation has a lipid transfer capacity and is proposed to directly transfer the lipid molecules from the ER to form autophagosomes. Vacuole membrane protein 1 (VMP1) and transmembrane protein 41b (TMEM41b) are ER membrane proteins that are associated with the formation of the subdomain. Recently, we have reported that an uncharacterized ER membrane protein possessing the DNAJ domain, called ERdj8/DNAJC16, is associated with the regulation of the size of autophagosomes. The localization of ERdj8/DNAJC16 partially overlaps with the PIS-enriched ER subdomain, thereby implying its association with autophagosome size determination. BioMed Central 2020-10-22 /pmc/articles/PMC7579975/ /pubmed/33087127 http://dx.doi.org/10.1186/s12929-020-00691-6 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Yamamoto, Yo-hei
Noda, Takeshi
Autophagosome formation in relation to the endoplasmic reticulum
title Autophagosome formation in relation to the endoplasmic reticulum
title_full Autophagosome formation in relation to the endoplasmic reticulum
title_fullStr Autophagosome formation in relation to the endoplasmic reticulum
title_full_unstemmed Autophagosome formation in relation to the endoplasmic reticulum
title_short Autophagosome formation in relation to the endoplasmic reticulum
title_sort autophagosome formation in relation to the endoplasmic reticulum
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7579975/
https://www.ncbi.nlm.nih.gov/pubmed/33087127
http://dx.doi.org/10.1186/s12929-020-00691-6
work_keys_str_mv AT yamamotoyohei autophagosomeformationinrelationtotheendoplasmicreticulum
AT nodatakeshi autophagosomeformationinrelationtotheendoplasmicreticulum