SLC7 transporters at the crossroads of amino acid metabolism and diabetes pathophysiology: insights and therapeutic perspectives

被引:0
作者
Xu, Tingting [1 ]
Zhang, Xiaoshi [1 ]
Chen, Qingqing [1 ]
Yang, Cheng [1 ]
Deng, Bo [1 ]
Armstrong, David G. [2 ]
Rui, Shunli [1 ]
Zhou, Yueqin [1 ]
Deng, Wuquan [1 ]
机构
[1] Chongqing Univ, Cent Hosp, Chongqing Emergency Med Ctr, Dept Endocrinol & Metab,Sch Med, Chongqing, Peoples R China
[2] Univ Southern Calif, Keck Sch Med, Dept Surg, Los Angeles, CA USA
关键词
SLC7; diabetes mellitus; amino acid transporters; metabolism; mechanisms; STIMULATED INSULIN-SECRETION; GLUCOSE-METABOLISM; SKELETAL-MUSCLE; IN-VITRO; MAGNETIC-RESONANCE; MASS-SPECTROMETRY; OXIDATIVE STRESS; BCAA CATABOLISM; LEUCINE; OBESITY;
D O I
10.3389/fnut.2025.1467057
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Amino acids are fundamental components of all living cells, serving not only as the building blocks of proteins but also as crucial sources of energy and precursors to key metabolites and signaling molecules. Amino acid transporters, specialized membrane proteins, facilitate the movement of amino acids across plasma membranes and between various cells and organ compartments. The malfunction, absence, or overexpression of specific amino acid transporters is linked to several human diseases. Among the extensive family of solute carrier proteins (SLCs), which comprises 458 transporters, the SLC7 transporter family, inclusive of CATs (Cationic Amino Acid Transporters) and LATs (L-type Amino Acid Transporters), is particularly instrumental in cellular amino acid uptake. Disruptions in amino acid transport can lead to significant metabolic abnormalities in diabetes, characterized by impaired insulin signaling and altered glucose metabolism. A deeper understanding of amino acid transporters' roles in metabolic processes and insulin signaling could shed light on the pathogenesis of diabetes and unveil novel therapeutic targets for this pervasive metabolic syndrome.
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页数:11
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共 182 条
[91]   Transporters Involved in Metformin Pharmacokinetics and Treatment Response [J].
Liang, Xiaomin ;
Giacomini, Kathleen M. .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2017, 106 (09) :2245-2250
[92]  
Liu GY, 2020, NAT REV MOL CELL BIO, V21, P183, DOI 10.1038/s41580-019-0199-y
[93]   Oxidative stress suppresses PHB2-mediated mitophagy in β-cells via the Nrf2/PHB2 pathway [J].
Liu, Shan ;
Zhang, Rui ;
Zhang, Lan ;
Yang, Aige ;
Guo, Yuqing ;
Jiang, Lei ;
Wang, Huijuan ;
Xu, Shunjiang ;
Zhou, Huimin .
JOURNAL OF DIABETES INVESTIGATION, 2024, 15 (05) :559-571
[94]   Reactive Oxygen and Nitrogen Species (RONS) and Cytokines-Myokines Involved in Glucose Uptake and Insulin Resistance in Skeletal Muscle [J].
Llanos, Paola ;
Palomero, Jesus .
CELLS, 2022, 11 (24)
[95]   Culture-induced changes in blood-brain barrier transcriptome: implications for amino-acid transporters in vivo [J].
Lyck, Ruth ;
Ruderisch, Nadine ;
Moll, Anton G. ;
Steiner, Oliver ;
Cohen, Clemens D. ;
Engelhardt, Britta ;
Makrides, Victoria ;
Verrey, Francois .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2009, 29 (09) :1491-1502
[96]   Branched-chain amino acids in metabolic signalling and insulin resistance [J].
Lynch, Christopher J. ;
Adams, Sean H. .
NATURE REVIEWS ENDOCRINOLOGY, 2014, 10 (12) :723-736
[97]   Skeletal Muscle Metabolism in the Pathology and Treatment of Type 1 Diabetes [J].
Mann, C. J. ;
Ayuso, E. ;
Anguela, X. M. ;
Bosch, F. .
CURRENT PHARMACEUTICAL DESIGN, 2010, 16 (08) :1002-1020
[98]   Role of mTOR in Glucose and Lipid Metabolism [J].
Mao, Zhuo ;
Zhang, Weizhen .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2018, 19 (07)
[99]   Hemocompatible LAT1-inhibitor can induce apoptosis in cancer cells without affecting brain amino acid homeostasis [J].
Markowicz-Piasecka, Magdalena ;
Huttunen, Johanna ;
Montaser, Ahmed ;
Huttunen, Kristiina M. .
APOPTOSIS, 2020, 25 (5-6) :426-440
[100]   Beyond the paradigm: Combining mass spectrometry and nuclear magnetic resonance for metabolomics [J].
Marshall, Darrell D. ;
Powers, Robert .
PROGRESS IN NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY, 2017, 100 :1-16