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Cited by 208Autophagy in Disease and TherapyPI3K/AKT/mTOR signaling in cancerMuscle metabolism and nutrition

The DOI matches its Crossref record; 56 of the 57 references it cites were found in a registry or an index.

Amino Acids and Insulin Control Autophagic Proteolysis through Different Signaling Pathways in Relation to mTOR in Isolated Rat Hepatocytes

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Kanazawa, Takumi, Taneike, Ikue, Akaishi, Ryuichiro, Yoshizawa, Fumiaki, Furuya, Norihiko, Fujimura, Shinobu, Kadowaki, Motoni·2004·Journal of Biological Chemistry
DOI 10.1074/jbc.m306337200
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Abstract

Autophagy, a major bulk proteolytic pathway, contributes to intracellular protein turnover, together with protein synthesis. Both are subject to dynamic control by amino acids and insulin. The mechanisms of signaling and cross-talk of their physiological anabolic effects remain elusive. Recent studies established that amino acids and insulin induce p70 S6 kinase (p70(S6k)) phosphorylation by mTOR, involved in translational control of protein synthesis. Here, the signaling mechanisms of amino acids and insulin in macroautophagy in relation to mTOR were investigated. In isolated rat hepatocytes, both regulatory amino acids (RegAA) and insulin coordinately activated p70(S6k) phosphorylation, which was completely blocked by rapamycin, an mTOR inhibitor. However, rapamycin blocked proteolytic suppression by insulin, but did not block inhibition by RegAA. These contrasting results suggest that insulin controls autophagy through the mTOR pathway, but amino acids do not. Furthermore, micropermeabilization with Saccharomyces aureus alpha-toxin completely deprived hepatocytes of proteolytic responsiveness to RegAA and insulin, but still maintained p70(S6k) phosphorylation by RegAA. In contrast, Leu(8)-MAP, a non-transportable leucine analogue, did not mimic the effect of leucine on p70(S6k) phosphorylation, but maintained the activity on proteolysis. Finally, BCH, a System L-specific amino acid, did not affect proteolytic suppression or mTOR activation by leucine. All the results indicate that mTOR is not common to the signaling mechanisms of amino acids and insulin in autophagy, and that the amino acid signaling starts extracellularly with their "receptor(s)," probably other than transporters, and is mediated through a novel route distinct from the mTOR pathway employed by insulin.

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Research works printed but not linked: 5

  1. Fafournoux, 2000, Biochem. J., 351, 1, 10.1042/bj3510001 · DOI
  2. van Sluijters, 2000, Biochem. J., 351, 545, 10.1042/bj3510545 · DOI
  3. Seglen, 1976, 13, 29
  4. Pacitti, 1993, Am. J. Physiol., 265, G90
  5. Shah, 2000, Am. J. Physiol., 279, E74

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Metadata

Authors
Kanazawa, T., Taneike, I., Akaishi, R., Yoshizawa, F., Furuya, N., Fujimura, S., & Kadowaki, M.
Affiliations
  • Niigata University (JP)
  • Utsunomiya University (JP)
Corresponding author
Kadowaki, Motoni
ORCID
Venue
Journal of Biological Chemistry
Publisher
Elsevier BV
Published
2004-02
Volume
279
Issue
9
Pages
8452-8459
ISSN
0021-9258 (ISSN-L)
DOI
10.1074/jbc.m306337200
OpenAlex
W2054125361
Cited by
208
References
57
Citations by year
2026: 1 · 2025: 2 · 2024: 1 · 2023: 1 · 2022: 5 · 2021: 7 · 2020: 6 · 2019: 13 · 2018: 5 · 2017: 10 · 2016: 7 · 2015: 8 · 2014: 16 · 2013: 12 · 2012: 9
FWCI
12.69
Type
journal article
Language
en
Open access
Licence
Locations
  • Journal of Biological Chemistry (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Autophagy in Disease and Therapy
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
  • Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
Keywords
autophagy, amino acids, insulin, mTOR, p70 S6 kinase, hepatocytes, leucine, rapamycin, protein turnover, amino acid signaling, alpha-toxin, BCH
MeSH terms
Amino Acids, Amino Acids, Cyclic, Animals, Bacterial Toxins, Cell Membrane, Enzyme Inhibitors, Hemolysin Proteins, Insulin, Leucine, Male, Peptide Hydrolases, Phosphorylation, Protein Kinases, Signal Transduction, Rats, Wistar, Sirolimus, Hepatocytes, Ribosomal Protein S6 Kinases, 70-kDa, Protein Kinase Inhibitors, Rats, TOR Serine-Threonine Kinases

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