Larson Mark K, Watson Steve P
Centre for Cardiovascular Sciences, Institute for Biomedical Research, University of Birmingham, United Kingdom.
Blood. 2006 Sep 1;108(5):1509-14. doi: 10.1182/blood-2005-11-011957. Epub 2006 May 2.
Mature megakaryocytes form structures called proplatelets that serve as conduits for platelet packaging and release at vascular sinusoids. Since the megakaryocyte expresses abundant levels of integrin alpha IIb beta3, we have examined a role for fibrinogen in proplatelet development and platelet release alongside that of other matrices. Primary mature murine megakaryocytes from bone marrow aspirates readily formed proplatelets when plated on fibrinogen at a degree that was significantly higher than that seen on other matrices. In addition, alpha IIb beta3 was essential for proplatelet formation on fibrinogen, as megakaryocytes failed to develop proplatelets in the presence of alpha IIb beta3 antagonists. Interestingly, inhibition of Src kinases or Ca2+ release did not inhibit proplatelet formation, indicating that alpha IIb beta3-mediated outside-in signals are not required for this response. Immunohistochemical studies demonstrated that fibrinogen is localized to the bone marrow sinusoids, a location that would allow it to readily influence platelet release. Further, thrombopoietin-stimulated alpha IIb-/- mice had a reduced increase in platelet number relative to controls. A similar observation was not observed for platelet recovery in alpha IIb-/- mice in response to antibody-induced thrombocytopenia, indicating the existence of additional pathways of regulation of proplatelet formation. These results demonstrate that fibrinogen is able to regulate proplatelet formation via integrin alpha IIb beta3.
成熟的巨核细胞形成称为前血小板的结构,这些结构作为血小板包装和在血管血窦处释放的通道。由于巨核细胞表达大量的整合素αIIbβ3,我们研究了纤维蛋白原在与其他基质一起的前血小板发育和血小板释放中的作用。当接种在纤维蛋白原上时,来自骨髓抽吸物的原代成熟小鼠巨核细胞很容易形成前血小板,其程度明显高于在其他基质上观察到的程度。此外,αIIbβ3对于在纤维蛋白原上形成前血小板至关重要,因为在存在αIIbβ3拮抗剂的情况下巨核细胞无法形成前血小板。有趣的是,抑制Src激酶或Ca2+释放并不抑制前血小板形成,这表明这种反应不需要αIIbβ3介导的由外向内信号。免疫组织化学研究表明纤维蛋白原定位于骨髓血窦,这一位置使其能够很容易地影响血小板释放。此外,血小板生成素刺激的αIIb-/-小鼠相对于对照的血小板数量增加减少。对于αIIb-/-小鼠对抗体诱导的血小板减少症的血小板恢复,未观察到类似的现象,这表明存在调节前血小板形成的其他途径。这些结果表明纤维蛋白原能够通过整合素αIIbβ3调节前血小板形成。