微rna调控的B细胞与肥胖有关。

Immunometabolism (Cobham (Surrey, England)) Pub Date : 2022-08-05 eCollection Date: 2022-07-01 DOI:10.1097/IN9.0000000000000005
Alyssa J Matz, Lili Qu, Keaton Karlinsey, Beiyan Zhou
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引用次数: 0

摘要

肥胖是一种普遍存在的健康风险,它会诱发慢性、低度炎症和胰岛素抵抗,部分原因是由激活的B细胞和其他常驻免疫细胞造成的脂肪组织炎症。然而,控制脂肪组织中b细胞活动的调节机制仍然知之甚少,限制了治疗创新。microrna是免疫细胞动力学的有效调节剂,通过在多个信号通路中微调下游基因网络。特别是,miR-150对b细胞发育至关重要,并通过调节脂肪组织b细胞功能抑制肥胖相关炎症。在此,我们回顾了microrna对b细胞发育、激活和功能的影响,并强调了mir -150调节的b细胞在肥胖过程中调节全身炎症和胰岛素抵抗的作用。通过这种方式,我们希望通过靶向microrna调节的b细胞行为来促进减轻肥胖引起的健康风险的转化发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MicroRNA-regulated B cells in obesity.

MicroRNA-regulated B cells in obesity.

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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