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首页> 外文期刊>International journal of hematology >Co-culture of hematopoietic stem cells with mesenchymal stem cells increases VCAM-1-dependent migration of primitive hematopoietic stem cells
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Co-culture of hematopoietic stem cells with mesenchymal stem cells increases VCAM-1-dependent migration of primitive hematopoietic stem cells

机译:造血干细胞与间充质干细胞的共培养增加了原始造血干细胞的VCAM-1依赖性迁移

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Hematopoietic stem cells (HSC) lose their capacity for engraftment during ex vivo cytokine expansion. It has been shown that mesenchymal stem cells (MSC) improve HSC transplantability; however, the molecular mechanisms responsible for this effect have not yet been completely elucidated. This paper reports that expanding HSC in co-culture with MSC enhances a vascular cell adhesion molecule (VCAM-1)-dependent pro-migratory phenotype. MSC did not regulate the HSC expression of CD49d (VCAM-1 counter-receptor molecule), but did decrease the cytokine-induced HSC VCAM-1-mediated pro-adhesive phenotype. Co-culture with MSC reduced the expression of the inactive conformation of lymphocyte function-associated antigen (LFA-1) at the HSC uropod, and induced higher expression of an LFA-1 activation epitope. Interestingly, VCAM-1-dependent HSC migration was modulated by targeting this LFA-1 high affinity form, suggesting integrin cross-regulation. VCAM-1-mediated HSC transmigration appeared to favor the more primitive HSC immunophenotype. Our results suggested that co-culture with MSC improved VCAM-1-dependent migration of primitive HSC, which was affected in ex vivo cytokine-expanded HSCs by a mechanism involving LFA-1 modulation.
机译:造血干细胞(HSC)在离体细胞因子扩增过程中丧失了其植入能力。研究表明,间充质干细胞(MSC)可改善HSC的移植性。但是,尚未完全阐明引起这种作用的分子机制。本文报道了在与MSC共培养中扩展HSC可以增强血管细胞粘附分子(VCAM-1)依赖性的促迁移表型。 MSC不能调节CD49d(VCAM-1反受体分子)的HSC表达,但可以降低细胞因子诱导的HSC VCAM-1介导的前黏附表型。与MSC共培养减少了HSC uropod淋巴细胞功能相关抗原(LFA-1)的失活构象的表达,并诱导了LFA-1激活表位的更高表达。有趣的是,通过靶向该LFA-1高亲和力形式来调节依赖VCAM-1的HSC迁移,表明整联蛋白交叉调控。 VCAM-1介导的HSC迁移似乎倾向于更原始的HSC免疫表型。我们的研究结果表明,与MSC的共培养改善了原始HSC的VCAM-1依赖性迁移,这受涉及LFA-1调节的机制在离体细胞因子扩增的HSC中影响。

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