The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Autophagy: The Last Defense against Cellular Nutritional Stress
Open accessAbstract
Homeostasis of nutrient metabolism is critical for maintenance of the normal physiologic status of the cell and the integral health of humans and mammals. In vivo, there is a highly efficient and precise process involved in nutrient recycling and organelle cleaning. This process is named autophagy, and it can be induced in response to the dynamic change of nutrients. When cells face nutritional stress, such as stress caused by nutrient deficiency or nutrient excess, the autophagy pathway will be activated. Generally, when nutrients are withdrawn, cells will sense the signs of starvation and respond. AMP-activated protein kinase and the mammalian target of rapamycin, two of the major metabolic kinases, are responsible for monitoring cellular energy and the concentration of amino acids, respectively. Nutrient excess also induces autophagy, mainly via the reactive oxygen species and endoplasmic reticulum stress pathway. When nutritional stress activates the autophagy pathway, the nutrients or damaged organelles will be recycled for cell survival. However, if autophagy is overwhelmingly induced, autophagic cell death will possibly occur. The balance of the autophagy induction is the crucial factor for cell survival or death. Herein, we summarize the current knowledge on the induction of autophagy, the autophagy response under nutritional stresses, and autophagic cell death and related diseases, which will highlight the process of nutritional stress-induced autophagy and its important physiologic and/or pathologic roles in cell metabolism and diseases, and shed light on the research into the mechanism and clinical applications of autophagy induced by nutritional stresses.
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Cites
AMPK and mTOR regulate autophagy through direct phosphorylation of Ulk1
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LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing.
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“RagA or RagB can bind to RagC or RagD to form the Rag complex (41), which is located on the lysosome membrane (42).”
BackgroundReactive oxygen species are essential for autophagy and specifically regulate the activity of Atg4
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“One study revealed that ROS accumulation is an essential element of autophagy induced by nutrient deficiency or rapamycin treatment (75).”
BackgroundULK-Atg13-FIP200 Complexes Mediate mTOR Signaling to the Autophagy Machinery
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AMP-activated protein kinase: an energy sensor that regulates all aspects of cell function
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Regulation of TORC1 by Rag GTPases in nutrient response
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Cited by
The Roles of Autophagy in Cancer
Yun, C. W., & Lee, S. H. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19113466 · Cited by 965
The interplay of ROS and the PI3K/Akt pathway in autophagy regulation
Kma, L., & Baruah, T. J. (2022) · Biotechnology and Applied Biochemistry · doi:10.1002/bab.2104 · Cited by 394
Inflammation and nutrition: friend or foe?
Stumpf, F., Keller, B., Gressies, C., & Schuetz, P. (2023) · Nutrients · doi:10.3390/nu15051159 · Cited by 213
Archaeal Histone Contributions to the Origin of Eukaryotes
Brunk, C. F., & Martin, W. F. (2019) · Trends in Microbiology · doi:10.1016/j.tim.2019.04.002 · Cited by 55
Metadata
- Authors
- He, L., Zhang, J., Zhao, J., Ma, N., Kim, S. W., Qiao, S., & Ma, X.
- Venue
- Advances in Nutrition
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 9
- Issue
- 4
- Pages
- 493-504
- ISSN
- 2156-5376 (ISSN-L)
- 2161-8313
- OpenAlex
- W2883479235
- Cited by
- 204
- References
- 27
- FWCI
- 11.93
- Type
- journal article
- Language
- en
- Open access
- bronze
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- He, L., Zhang, J., Zhao, J., Ma, N., Kim, S. W., Qiao, S., & Ma, X. (2018). Autophagy: The Last Defense against Cellular Nutritional Stress. Advances in Nutrition. https://doi.org/10.1093/advances/nmy011
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