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首页> 外文期刊>Diabetes research and clinical practice >Human umbilical cord blood-derived mesenchymal stem cells prevent diabetic renal injury through paracrine action
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Human umbilical cord blood-derived mesenchymal stem cells prevent diabetic renal injury through paracrine action

机译:人脐带血间充质干细胞通过旁分泌作用预防糖尿病性肾损伤

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Aims: The present study examined renoprotective effect of human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSC) in diabetes. NRK-52E cells were utilized to determine the paracrine effect of hUCB-MSC. Methods: hUCB was harvested with the mother's consent. MSC obtained from the hUCB were injected through the tail vein. Growth arrested and synchronized NRK-52E cells were stimulated with transforming growth factor-β1 (TGF-β1) in the presence of hUCB-MSC conditioned media. Results: At 4 weeks after the streptozotocin (STZ) injection, diabetic rats showed significantly increased urinary protein excretion, renal and glomerular hypertrophy, fractional mesangial area, renal expression of TGF-β1 and α-smooth muscle actin, and collagen accumulation but decreased renal E-cadherin and bone morphogenic protein-7 expression, confirming diabetic renal injury. hUCB-MSC effectively prevented diabetic renal injury except renal and glomerular hypertrophy without a significant effect on blood glucose. CM-DiI-labeled hUCB-MSC and immunostaining of PKcs, a human nuclei antigen, confirmed a few engraftment of hUCB-MSC in diabetic kidneys. hUCB-MSC conditioned media inhibited TGF-β1-induced extracellular matrix upregulation and epithelial-to-mesenchymal transition in NRK-52E cells in a concentration-dependent manner. Conclusions: These results demonstrate the renoprotective effect of hUCB-MSC in STZ-induced diabetic rats possibly through secretion of humoral factors and suggest hUCB-MSC as a possible treatment modality for diabetic renal injury.
机译:目的:本研究研究了人脐带血间充质干细胞(hUCB-MSC)在糖尿病中的肾脏保护作用。 NRK-52E细胞用于确定hUCB-MSC的旁分泌作用。方法:在母亲的同意下收集hUCB。从hUCB获得的MSC通过尾静脉注射。在hUCB-MSC条件培养基存在下,用转化生长因子-β1(TGF-β1)刺激生长停滞和同步的NRK-52E细胞。结果:链脲佐菌素(STZ)注射后4周,糖尿病大鼠的尿蛋白排泄,肾和肾小球肥大,肾小球系膜面积,TGF-β1和α-平滑肌肌动蛋白的肾脏表达显着增加,胶原蛋白积聚但肾脏减少E-cadherin和骨形态发生蛋白7的表达,证实了糖尿病肾损害。 hUCB-MSC可有效预防糖尿病肾损害,但肾和肾小球肥大除外,对血糖无明显影响。 CM-DiI标记的hUCB-MSC和人核抗原PKcs的免疫染色证实了hUCB-MSC在糖尿病肾中的一些移入。 hUCB-MSC条件培养基以浓度依赖性方式抑制NRK-52E细胞中TGF-β1诱导的细胞外基质上调和上皮-间充质转化。结论:这些结果证明了hUCB-MSC在STZ诱导的糖尿病大鼠中的肾脏保护作用可能是通过分泌体液因子而引起的,并提示hUCB-MSC是糖尿病性肾损伤的一种可能的治疗方式。

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