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The Mechanisms of M-cell Differentiation

机译:M细胞分化的机制

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摘要

Intestinal M (microfold or membranous) cells are an enigmatic lineage of intestinal epithelial cells that initiate mucosal immune responses through the uptake and transcytosis of luminal antigens. Due to their rarity, the mechanisms of M-cell function and differentiation are poorly understood. To overcome this problem, experimental strategies to enrich for M-cells have been established. Transcriptome analyses have provided valuable insight, especially on the receptors for antigen uptake, and such studies have broadened our knowledge of M-cell function. In another line of investigation, we and others have begun to dissect the molecular pathways of M-cell differentiation. Among them, receptor activator of NF-κB ligand (RANKL) has been identified as an essential factor for M-cell differentiation. We have focused on the M-cell inducible activity of RANKL and have been able to observe temporal transitions during M-cell differentiation by using in vivo ectopic M-cell differentiation induced by exogenous RANKL treatment. We have found that the ets-family transcription factor Spi-B is essential for functional maturation of M cells. In the absence of Spi-B, the immune response to Salmonella Typhimurium is severely impaired, suggesting that M cells are important for maintaining intestinal homeostasis.
机译:肠M(微折叠或膜性)细胞是肠上皮细胞的神秘谱系,其通过腔内抗原的摄取和胞吞作用启动粘膜免疫反应。由于它们的稀有性,人们对M细胞功能和分化的机制知之甚少。为了克服该问题,已经建立了富集M细胞的实验策略。转录组分析提供了宝贵的见解,尤其是在抗原摄取受体方面,这些研究拓宽了我们对M细胞功能的了解。在另一研究领域,我们和其他人已开始剖析M细胞分化的分子途径。其中,NF-κB配体的受体激活剂(RANKL)已被确定为M细胞分化的重要因素。我们专注于RANKL的M细胞诱导活性,并能够通过使用由外源性RANKL治疗诱导的体内异位M细胞分化来观察M细胞分化过程中的时间变化。我们发现,ets家族转录因子Spi-B对于M细胞的功能成熟至关重要。在没有Spi-B的情况下,对鼠伤寒沙门氏菌的免疫反应会严重受损,这表明M细胞对于维持肠道稳态非常重要。

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