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Chemically primed bone-marrow derived mesenchymal stem cells show enhanced expression of chemokine receptors contributed to their migration capability

机译:化学启动的骨髓来源的间充质干细胞显示趋化因子受体的表达增强有助于其迁移能力

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摘要

Objective(s):The limited homing potential of bone-marrow-derived mesenchymal stem cells (BM-MSC) is the key obstacle in MSC-based therapy. It is believed that chemokines and chemokine receptor interactions play key roles in cellular processes associated with migration. Meanwhile, MSCs express a low level of distinct chemokine receptors and they even lose these receptors on their surface after a few passages which influence their therapeutic applications negatively. This study investigated whether treatment of BM-MSCs with hypoxia-mimicking agents would increase expression of some chemokine receptors and cell migration.
机译:目的:骨髓间充质干细胞(BM-MSC)的归巢潜力有限是基于MSC的治疗的主要障碍。据信趋化因子和趋化因子受体相互作用在与迁移相关的细胞过程中起关键作用。同时,MSC表达低水平的不同趋化因子受体,甚至经过数次传代后它们甚至在表面上丢失这些受体,从而不利地影响了它们的治疗应用。这项研究调查了用缺氧模拟剂治疗BM-MSC是否会增加某些趋化因子受体的表达和细胞迁移。

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