首页> 外文期刊>Basic Research in Cardiology: Official Journal of the German Association of Cardiovascular Research >Time course of myocardial stromal cell-derived factor 1 expression and beneficial effects of intravenously administered bone marrow stem cells in rats with experimental myocardial infarction.
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Time course of myocardial stromal cell-derived factor 1 expression and beneficial effects of intravenously administered bone marrow stem cells in rats with experimental myocardial infarction.

机译:心肌基质细胞衍生因子1表达的时程以及静脉注射骨髓干细胞对实验性心肌梗死大鼠的有益作用。

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OBJECTIVE: The chemokine stromal cell-derived factor-1 (SDF-1) has been implicated in homing of bone marrow cells to sites of injury. We investigated the time course of myocardial SDF-1 expression and effects of intravenously administered bone marrow mesenchymal stem cells (MSC) in rats with myocardial infarction (MI). METHODS: SDF-1 expression was measured by RT-PCR and Western blot in sham operated or infarcted hearts at 1/2, 1, 2, 4, 8 and 16 days post operation. MSCs from donor rats were labeled with BrdU. A total of 5 x 10(6) cells in 2.5 mL of PBS or equal volume PBS alone were injected through the tail vein at above mentioned time points. The number of the labeled MSCs in the infarcted hearts was counted 3 days post injection. Cardiac function and vessel numbers were assessed 28 days post injection. RESULTS: Myocardial SDF-1 expression increased and peaked at the first day and decreased thereafter post MI and remained unchanged in sham operated hearts. The MSCs enrichment and angiogenesis in thehost hearts were more abundant in the 1 day transplantation group than in the other groups (P < 0.01). Cardiac function was only improved in rats received intravenous MSCs injection within 4 days post MI and not affected by PBS injection. CONCLUSIONS: Myocardial SDF-1 expression was increased only in the early phase post MI. MSCs intravenous infused at the early phase of MI were recruited to injured heart, enhanced angiogenesis and improved cardiac function.
机译:目的:趋化因子基质细胞衍生因子1(SDF-1)与骨髓细胞归巢到损伤部位有关。我们调查了心肌梗死(MI)大鼠心肌SDF-1表达的时程和静脉给药骨髓间充质干细胞(MSC)的影响。方法:通过RT-PCR和Western blot检测假手术或梗死后心脏在手术后1 / 2、1、2、4、8和16天的SDF-1表达。用BrdU标记来自供体大鼠的MSC。在上述时间点通过尾静脉注射仅2.5 mL PBS或等体积PBS中的总共5 x 10(6)细胞。注射后3天计数梗死心脏中标记的MSC的数量。注射后28天评估心脏功能和血管数目。结果:心肌梗死后第一天,心肌SDF-1表达增加并达到峰值,此后下降,并且在假手术心脏中保持不变。在第1天移植组中,宿主心脏中MSC的富集和血管生成比其他组更丰富(P <0.01)。心功能仅在心肌梗死后4天内接受静脉MSCs注射的大鼠中有所改善,而不受PBS注射的影响。结论:心肌梗死后早期,心肌SDF-1表达增加。在心肌梗死早期静脉输注的MSCs被募集到受伤的心脏,增强血管生成和改善心脏功能。

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