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MicroRNA-regulated B cells in obesity.
Matz, Alyssa J; Qu, Lili; Karlinsey, Keaton; Zhou, Beiyan.
Afiliação
  • Matz AJ; Department of Immunology, School of Medicine, University of Connecticut, Farmington, CT, USA.
  • Qu L; Department of Immunology, School of Medicine, University of Connecticut, Farmington, CT, USA.
  • Karlinsey K; Department of Immunology, School of Medicine, University of Connecticut, Farmington, CT, USA.
  • Zhou B; Department of Immunology, School of Medicine, University of Connecticut, Farmington, CT, USA.
Immunometabolism (Cobham) ; 4(3): e00005, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35966635
ABSTRACT
Obesity is a prevalent health risk by inducing chronic, low-grade inflammation and insulin resistance, in part from adipose tissue inflammation perpetuated by activated B cells and other resident immune cells. However, regulatory mechanisms controlling B-cell actions in adipose tissue remain poorly understood, limiting therapeutic innovations. MicroRNAs are potent regulators of immune cell dynamics through fine-tuning a network of downstream genes in multiple signaling pathways. In particular, miR-150 is crucial to B-cell development and suppresses obesity-associated inflammation via regulating adipose tissue B-cell function. Herein, we review the effect of microRNAs on B-cell development, activation, and function and highlight miR-150-regulated B-cell actions during obesity which modulate systemic inflammation and insulin resistance. In this way, we hope to promote translational discoveries that mitigate obesity-induced health risks by targeting microRNA-regulated B-cell actions.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article