血小板生成素配体:生物活性。

F Wendling, K Cohen-Solal, J L Villeval, N Debili, W Vainchenker
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引用次数: 2

摘要

血小板生成素(TPO)或Mpl配体是血小板产生的主要生理调节剂。该细胞因子是体外培养MK祖细胞和前体细胞增殖和分化的最有效刺激物。它还与几种细胞因子一起作用于各种造血谱系的祖细胞,包括原始干细胞。当给药于正常动物时,该因子是一种非常有效的血小板生成剂,在几种骨髓抑制模型中,它可以加速血小板和红细胞生成的恢复。I/II期临床试验正在进行中,未发现不良反应。Mpl配体不诱导血小板聚集,但降低血小板对激动剂生理剂量的敏感性。在实验小鼠模型中,高剂量和慢性剂量的Mpl配体导致骨髓纤维化。TPO不断由肝脏和肾脏产生;它通过与巨核细胞和血小板上表达的受体结合而在血浆中清除。然而,这种新的细胞因子的全部生物学效应尚未完全了解,特别是它在血小板产生的终末阶段的作用。在不久的将来,可能会在人类异常血小板产生的生理病理机制方面获得新的见解。
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Mpl ligand or thrombopoietin: biological activities.

Thrombopoietin (TPO) or Mpl ligand is the primary physiological regulator of platelet production. This cytokine is the most potent stimulator of the proliferation and differentiation of MK progenitor and precursor cells in vitro. It also acts additively or synergistically with several cytokines on progenitor cells from various hematopoietic lineages, including the primitive stem cells. The factor is an extremely potent thrombocytopoietic agent when administrated to normal animals, and it accelerates platelet and erythropoietic recovery in several models of myelosuppression. Phase I/II clinical trials are ongoing with no detectable adverse effects. Mpl ligand does not induce platelet aggregation, but it lowers the platelet sensitivity to physiological dose of agonists. In experimental mouse models, high and chronic dose of Mpl ligand results in myelofibrosis. TPO is constantly produced by the liver and the kidney; its plasmatic clearance occurs by binding to its receptor expressed on megakaryocytes and platelets. However, the full spectrum of the biological effects of this new cytokine is not fully understood, in particular its the role in the terminal stage of platelet production. In the near future, it is likely that new insights will be obtained in the physiopathological mechanisms underlying abnormal platelet production in human.

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