TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes

Mitochondria, the organelle critical for cell survival and metabolism, are exploited by cancer cells and provide an important therapeutic target in cancers. Mitochondria dynamically undergo fission and fusion to maintain their diverse functions. Proteins controlling mitochondrial fission and fusion...

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Main Authors: Jaeyong Jung, Samantha Gokhale, Ping Xie
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-01-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1081253/full
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author Jaeyong Jung
Jaeyong Jung
Samantha Gokhale
Samantha Gokhale
Ping Xie
Ping Xie
author_facet Jaeyong Jung
Jaeyong Jung
Samantha Gokhale
Samantha Gokhale
Ping Xie
Ping Xie
author_sort Jaeyong Jung
collection DOAJ
description Mitochondria, the organelle critical for cell survival and metabolism, are exploited by cancer cells and provide an important therapeutic target in cancers. Mitochondria dynamically undergo fission and fusion to maintain their diverse functions. Proteins controlling mitochondrial fission and fusion have been recognized as essential regulators of mitochondrial functions, mitochondrial quality control, and cell survival. In a recent proteomic study, we identified the key mitochondrial fission factor, MFF, as a new interacting protein of TRAF3, a known tumor suppressor of multiple myeloma and other B cell malignancies. This interaction recruits the majority of cytoplasmic TRAF3 to mitochondria, allowing TRAF3 to regulate mitochondrial morphology, mitochondrial functions, and mitochondria-dependent apoptosis in resting B lymphocytes. Interestingly, recent transcriptomic, metabolic and lipidomic studies have revealed that TRAF3 also vitally regulates multiple metabolic pathways in B cells, including phospholipid metabolism, glucose metabolism, and ribonucleotide metabolism. Thus, TRAF3 emerges as a novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes and B cell malignancies. Here we review current knowledge in this area and discuss relevant clinical implications.
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spelling doaj.art-2dccde1db6f24d2a89890389d5e1f0b42023-01-27T05:18:02ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-01-011310.3389/fonc.2023.10812531081253TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytesJaeyong Jung0Jaeyong Jung1Samantha Gokhale2Samantha Gokhale3Ping Xie4Ping Xie5Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, United StatesGraduate Program in Cellular and Molecular Pharmacology, Rutgers University, Piscataway, NJ, United StatesDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, United StatesGraduate Program in Cellular and Molecular Pharmacology, Rutgers University, Piscataway, NJ, United StatesDepartment of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ, United StatesRutgers Cancer Institute of New Jersey, New Brunswick, NJ, United StatesMitochondria, the organelle critical for cell survival and metabolism, are exploited by cancer cells and provide an important therapeutic target in cancers. Mitochondria dynamically undergo fission and fusion to maintain their diverse functions. Proteins controlling mitochondrial fission and fusion have been recognized as essential regulators of mitochondrial functions, mitochondrial quality control, and cell survival. In a recent proteomic study, we identified the key mitochondrial fission factor, MFF, as a new interacting protein of TRAF3, a known tumor suppressor of multiple myeloma and other B cell malignancies. This interaction recruits the majority of cytoplasmic TRAF3 to mitochondria, allowing TRAF3 to regulate mitochondrial morphology, mitochondrial functions, and mitochondria-dependent apoptosis in resting B lymphocytes. Interestingly, recent transcriptomic, metabolic and lipidomic studies have revealed that TRAF3 also vitally regulates multiple metabolic pathways in B cells, including phospholipid metabolism, glucose metabolism, and ribonucleotide metabolism. Thus, TRAF3 emerges as a novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes and B cell malignancies. Here we review current knowledge in this area and discuss relevant clinical implications.https://www.frontiersin.org/articles/10.3389/fonc.2023.1081253/fullTRAF3mitochondriametabolismB lymphocyteslymphomas
spellingShingle Jaeyong Jung
Jaeyong Jung
Samantha Gokhale
Samantha Gokhale
Ping Xie
Ping Xie
TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
Frontiers in Oncology
TRAF3
mitochondria
metabolism
B lymphocytes
lymphomas
title TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
title_full TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
title_fullStr TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
title_full_unstemmed TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
title_short TRAF3: A novel regulator of mitochondrial physiology and metabolic pathways in B lymphocytes
title_sort traf3 a novel regulator of mitochondrial physiology and metabolic pathways in b lymphocytes
topic TRAF3
mitochondria
metabolism
B lymphocytes
lymphomas
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1081253/full
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AT samanthagokhale traf3anovelregulatorofmitochondrialphysiologyandmetabolicpathwaysinblymphocytes
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AT pingxie traf3anovelregulatorofmitochondrialphysiologyandmetabolicpathwaysinblymphocytes
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