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A global view of T cell metabolism in systemic lupus erythematosus.
Goetz, Andrew; Cagmat, Joy; Brusko, Maigan; Brusko, Todd M; Rushin, Anna; Merritt, Matthew; Garrett, Timothy; Morel, Laurence; Dixit, Purushottam.
Afiliação
  • Goetz A; Department of Biomedical Engineering, Yale University, New Haven, CT, United States.
  • Cagmat J; Department of Pathology, University of Florida, Gainesville, FL, United States.
  • Brusko M; Department of Pathology, University of Florida, Gainesville, FL, United States.
  • Brusko TM; Department of Pathology, University of Florida, Gainesville, FL, United States.
  • Rushin A; Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States.
  • Merritt M; Department of Biochemistry and Molecular Biology, University of Florida, Gainesville, FL, United States.
  • Garrett T; Department of Pathology, University of Florida, Gainesville, FL, United States.
  • Morel L; Department of Microbiology, Immunology & Molecular Genetics, University of Texas (UT) Health San Antonio, TX, United States.
  • Dixit P; Department of Biomedical Engineering, Yale University, New Haven, CT, United States.
Front Immunol ; 15: 1371708, 2024.
Article em En | MEDLINE | ID: mdl-38756769
ABSTRACT
Impaired metabolism is recognized as an important contributor to pathogenicity of T cells in Systemic Lupus Erythematosus (SLE). Over the last two decades, we have acquired significant knowledge about the signaling and transcriptomic programs related to metabolic rewiring in healthy and SLE T cells. However, our understanding of metabolic network activity derives largely from studying metabolic pathways in isolation. Here, we argue that enzymatic activities are necessarily coupled through mass and energy balance constraints with in-built network-wide dependencies and compensation mechanisms. Therefore, metabolic rewiring of T cells in SLE must be understood in the context of the entire network, including changes in metabolic demands such as shifts in biomass composition and cytokine secretion rates as well as changes in uptake/excretion rates of multiple nutrients and waste products. As a way forward, we suggest cell physiology experiments and integration of orthogonal metabolic measurements through computational modeling towards a comprehensive understanding of T cell metabolism in lupus.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Lúpus Eritematoso Sistêmico Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Linfócitos T / Lúpus Eritematoso Sistêmico Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article