Ruffinatto Lucas, Groult Yann, Iacono Johanna, Sarrazin Sandrine, de Laval Bérengère
Aix Marseille University, Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Centre d'Immunologie de Marseille-Luminy (CIML), Marseille, France.
Front Immunol. 2024 Dec 10;15:1491729. doi: 10.3389/fimmu.2024.1491729. eCollection 2024.
Hematopoietic stem cells (HSCs) are a rare, long-lived and multipotent population that give rise to majority of blood cells and some tissue-resident immune cells. There is growing evidence that inflammatory stimuli can trigger persistent reprogramming in HSCs that enhances or inhibits the cellular functions of these HSCs and their progeny in response to subsequent infections. This newly discovered property makes HSCs a reservoir for innate immune memory. The molecular mechanisms underlying innate immune memory in HSCs are similar to those observed in innate immune cells, although their full elucidation is still pending. In this review, we examine the current state of knowledge on how an inflammatory response leads to reprogramming of HSCs. Understanding the full spectrum of consequences of reshaping early hematopoiesis is critical for assessing the potential benefits and risks under physiological and pathological conditions.
造血干细胞(HSCs)是一种罕见、长寿且具有多能性的细胞群体,可产生大多数血细胞和一些组织驻留免疫细胞。越来越多的证据表明,炎症刺激可触发造血干细胞的持续性重编程,从而增强或抑制这些造血干细胞及其子代细胞在应对后续感染时的细胞功能。这一最新发现的特性使造血干细胞成为先天性免疫记忆的储存库。造血干细胞中先天性免疫记忆的分子机制与先天性免疫细胞中观察到的机制相似,尽管其全面阐释仍有待完成。在这篇综述中,我们研究了关于炎症反应如何导致造血干细胞重编程的当前知识状态。了解重塑早期造血过程的全部后果对于评估生理和病理条件下的潜在益处和风险至关重要。