脂质和脂蛋白对动脉粥样硬化中造血细胞代谢和功能的影响。

Andrea Baragetti, Fabrizia Bonacina, Alberico Luigi Catapano, Giuseppe Danilo Norata
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引用次数: 15

摘要

造血是导致骨髓内产生多种白细胞谱系的过程。由于造血干细胞(hsc)的非随机分裂,这一过程在整个生命过程中得以维持,在每次分裂过程中,一个子细胞保持多能性,而另一个子细胞分化为一个受限的多能祖细胞(MPP),后者转化为成熟的循环细胞。这一过程在细胞代谢水平上受到严格调控,从静止HSC的典型厌氧糖酵解到氧化代谢的转变促进了HSC的增殖和承诺。影响代谢的全身和局部因素在病理条件下改变造血干细胞的平衡,慢性代谢和炎症性疾病驱使造血干细胞向活化的血液免疫细胞亚群转移。这就是动脉粥样硬化的情况,在动脉粥样硬化中,受损的全身脂质代谢影响hsc的表观遗传学,反映为向活化的循环亚群分化增加。本文就脂质和脂蛋白对造血干细胞病理生理的影响进行综述,重点讨论影响细胞代谢的分子机制。更好地了解这些方面将有助于制定针对动脉粥样硬化相关炎症的创新策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of Lipids and Lipoproteins on Hematopoietic Cell Metabolism and Commitment in Atherosclerosis.

Effect of Lipids and Lipoproteins on Hematopoietic Cell Metabolism and Commitment in Atherosclerosis.

Effect of Lipids and Lipoproteins on Hematopoietic Cell Metabolism and Commitment in Atherosclerosis.

Effect of Lipids and Lipoproteins on Hematopoietic Cell Metabolism and Commitment in Atherosclerosis.

Hematopoiesis is the process that leads to multiple leukocyte lineage generation within the bone marrow. This process is maintained throughout life thanks to a nonstochastic division of hematopoietic stem cells (HSCs), where during each division, one daughter cell retains pluripotency while the other differentiates into a restricted multipotent progenitor (MPP) that converts into mature, committed circulating cell. This process is tightly regulated at the level of cellular metabolism and the shift from anaerobic glycolysis, typical of quiescent HSC, to oxidative metabolism fosters HSCs proliferation and commitment. Systemic and local factors influencing metabolism alter HSCs balance under pathological conditions, with chronic metabolic and inflammatory diseases driving HSCs commitment toward activated blood immune cell subsets. This is the case of atherosclerosis, where impaired systemic lipid metabolism affects HSCs epigenetics that reflects into increased differentiation toward activated circulating subsets. Aim of this review is to discuss the impact of lipids and lipoproteins on HSCs pathophysiology, with a focus on the molecular mechanisms influencing cellular metabolism. A better understanding of these aspects will shed light on innovative strategies to target atherosclerosis-associated inflammation.

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