Blin Antoine, Le Goff Anne, Magniez Aurélie, Poirault-Chassac Sonia, Teste Bruno, Sicot Géraldine, Nguyen Kim Anh, Hamdi Feriel S, Reyssat Mathilde, Baruch Dominique
PlatOD, Paris, France.
MMN, UMR CNRS 7083 Gulliver, ESPCI Paris, PSL Research University, 10 rue Vauquelin, 75005 Paris, France.
Sci Rep. 2016 Feb 22;6:21700. doi: 10.1038/srep21700.
We present a new, rapid method for producing blood platelets in vitro from cultured megakaryocytes based on a microfluidic device. This device consists in a wide array of VWF-coated micropillars. Such pillars act as anchors on megakaryocytes, allowing them to remain trapped in the device and subjected to hydrodynamic shear. The combined effect of anchoring and shear induces the elongation of megakaryocytes and finally their rupture into platelets and proplatelets. This process was observed with megakaryocytes from different origins and found to be robust. This original bioreactor design allows to process megakaryocytes at high throughput (millions per hour). Since platelets are produced in such a large amount, their extensive biological characterisation is possible and shows that platelets produced in this bioreactor are functional.
我们展示了一种基于微流控装置从培养的巨核细胞体外快速生产血小板的新方法。该装置由大量涂有血管性血友病因子(VWF)的微柱组成。这些微柱可作为巨核细胞的锚定物,使它们被困在装置中并受到流体动力剪切力作用。锚定和剪切的联合作用会诱导巨核细胞伸长,最终使其破裂形成血小板和前血小板。在来自不同来源的巨核细胞上观察到了这一过程,并且发现该过程具有稳定性。这种独特的生物反应器设计能够以高通量(每小时数百万个)处理巨核细胞。由于能产生大量血小板,因此可以对其进行广泛的生物学特性表征,结果表明在这种生物反应器中产生的血小板具有功能。