Amino acids-Rab1A-mTORC1 signaling controls whole-body glucose homeostasis.
Amino Acids
/ metabolism
Animals
Cell Nucleus
/ metabolism
Diabetes Mellitus, Type 2
/ metabolism
Down-Regulation
Glucose
/ metabolism
Glucose Intolerance
/ complications
Homeodomain Proteins
/ metabolism
Homeostasis
Hyperglycemia
/ metabolism
Insulin
/ genetics
Insulin Secretion
Islets of Langerhans
/ metabolism
Mechanistic Target of Rapamycin Complex 1
/ metabolism
Mice, Inbred C57BL
Models, Biological
Organ Specificity
Protein Stability
Protein Transport
Signal Transduction
Trans-Activators
/ metabolism
Transcription, Genetic
rab1 GTP-Binding Proteins
/ metabolism
PDX1
Rab1A
alpha-cell
amino acids
beta-cell
diabetes
glucose homeostasis
insulin
mTOR
trans-differentiation
Journal
Cell reports
ISSN: 2211-1247
Titre abrégé: Cell Rep
Pays: United States
ID NLM: 101573691
Informations de publication
Date de publication:
16 03 2021
16 03 2021
Historique:
received:
01
09
2020
revised:
28
12
2020
accepted:
16
02
2021
entrez:
17
3
2021
pubmed:
18
3
2021
medline:
27
1
2022
Statut:
ppublish
Résumé
Rab1A is a small GTPase known for its role in vesicular trafficking. Recent evidence indicates that Rab1A is essential for amino acids (aas) sensing and signaling to regulate mTORC1 in normal and cancer cells. However, Rab1A's in vivo function in mammals is not known. Here, we report the generation of tamoxifen (TAM)-induced whole body Rab1A knockout (Rab1A
Identifiants
pubmed: 33730578
pii: S2211-1247(21)00144-3
doi: 10.1016/j.celrep.2021.108830
pmc: PMC8062038
mid: NIHMS1684385
pii:
doi:
Substances chimiques
Amino Acids
0
Homeodomain Proteins
0
Insulin
0
Trans-Activators
0
pancreatic and duodenal homeobox 1 protein
0
Mechanistic Target of Rapamycin Complex 1
EC 2.7.11.1
rab1 GTP-Binding Proteins
EC 3.6.5.2
Glucose
IY9XDZ35W2
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
108830Subventions
Organisme : NCI NIH HHS
ID : R01 CA173519
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK124897
Pays : United States
Informations de copyright
Copyright © 2021 The Author(s). Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests The authors declare no competing interests.
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