血块变厚:造血干细胞对老年血小板生物学贡献的最新线索提出了新问题。

Advances in geriatric medicine and research Pub Date : 2021-01-01 Epub Date: 2021-10-28 DOI:10.20900/agmr20210019
Donna M Poscablo, E Camilla Forsberg
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引用次数: 0

摘要

血小板能阻止体内外出血,从而起到挽救生命的作用。然而,血小板生物学也有其阴暗面。最近的报告提供了小鼠和人类衰老过程中血小板反应性增加的证据,使血小板成为心血管疾病、中风和癌症等人类最常见的衰老相关病症的主要嫌疑人。是什么导致了衰老过程中血小板的高反应性?在此,我们将讨论造血干细胞分化为血小板系的途径如何为了解年轻和衰老血小板之间的根本差异提供了途径。最近的研究进展开始揭示母体造血干细胞和祖细胞的细胞和分子调控如何可能将衰老特征赋予由此产生的血小板祖细胞。由此产生的对血小板内在反应性的机理认识,将为选择性地针对与年龄有关的途径提供策略。这篇简短的文章重点介绍了目前有关衰老造血的概念以及衰老过程中血小板过度活跃的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Clot Thickens: Recent Clues on Hematopoietic Stem Cell Contribution to Age-Related Platelet Biology Open New Questions.

Platelets provide life-saving functions by halting external and internal bleeding. There is also a dark side to platelet biology, however. Recent reports provide evidence for increased platelet reactivity during aging of mice and humans, making platelets main suspects in the most prevalent aging-related human pathologies, including cardiovascular diseases, stroke, and cancer. What drives this platelet hyperreactivity during aging? Here, we discuss how hematopoietic stem cell differentiation pathways into the platelet lineage offer avenues to understand the fundamental differences between young and old platelets. Recent advances begin to unravel how the cellular and molecular regulation of the parent hematopoietic stem and progenitor cells likely imbue aging characteristics on the resulting Plt progeny. The resulting mechanistic insights into intrinsic platelet reactivity will provide strategies for selectively targeting age-related pathways. This brief viewpoint focuses on current concepts on aging hematopoiesis and the implications for platelet hyperactivity during aging.

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