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Transplantation of differentiated umbilical cord mesenchymal cells under kidney capsule for control of type I diabetes in rat

机译:肾囊膜下分化脐带间充质细胞移植控制大鼠I型糖尿病

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Nowadays, stem cells have been introduced as an appropriate source of regenerative medicine for treatment of type I diabetes. Human umbilical cord matrix-derived mesenchymal cells (hUCMC) have successfully been differentiated into insulin producing cells. The isolated hUCM cells were characterized by the expression of stem cell surface markers and by differentiation into adipocytes and osteocytes. The hUCMCs were cultured with different concentrations of neural conditional medium (NCM) and were induced to differentiate into insulin producing cells (IPCs). As 60% NCM concentration resulted in higher nestin and PDX1 expression, the cells were first exposed to 60% NCM and were then induced for IPCs differentiation. PDX1 and insulin gene expression was evaluated in the treated cells. Also, the secretion capacity of the IPCs was assessed by glucose challenge test. IPCs were transferred under the rat kidney capsule. Blood glucose level, weight gain and immunohistochemistry assessments were done in the treated animals. hUCMC expressed mesenchymal cell surface markers and successfully differentiated into adipocytes and osteocytes. Higher NCM concentration resulted in higher PDX1 and nestin expression. The IPCs expressed insulin and PDX1. IPCs were detectable under the kidney capsule 2 months after injection. IPCs transplantation resulted in a sharp decline of blood sugar level and less weight loss. Differentiated hUCM cells could alleviate the insulin deprivation in the rat model of type I diabetes. In addition, higher NCM concentration leads to more differentiation into IPCs and more nestin and PDX1 expression. Kidney capsule can serve as a suitable nominee for IPCs transplantation. (C) 2015 Elsevier Ltd. All rights reserved.
机译:如今,干细胞已被引入作为治疗I型糖尿病的合适再生医学来源。人脐带基质来源的间充质细胞(hUCMC)已成功分化为产生胰岛素的细胞。分离的hUCM细胞的特征在于干细胞表面标志物的表达以及分化为脂肪细胞和骨细胞。用不同浓度的神经条件培养基(NCM)培养hUCMC,并诱导其分化为胰岛素产生细胞(IPC)。由于60%NCM浓度会导致较高的巢蛋白和PDX1表达,因此首先将细胞暴露于60%NCM,然后诱导其进行IPC分化。在处理的细胞中评估PDX1和胰岛素基因表达。另外,通过葡萄糖激发试验评估了IPC的分泌能力。将IPC转移到大鼠肾囊下。在治疗的动物中进行血糖水平,体重增加和免疫组织化学评估。 hUCMC表达间充质细胞表面标志物,并成功分化为脂肪细胞和骨细胞。较高的NCM浓度导致较高的PDX1和Nestin表达。 IPC表达胰岛素和PDX1。注射后2个月,在肾囊下可检测到IPC。 IPCs移植导致血糖水平急剧下降且体重减轻较少。分化的hUCM细胞可以减轻I型糖尿病大鼠模型中的胰岛素剥夺。此外,较高的NCM浓度导致更多地分化为IPC,以及更多的Nestin和PDX1表达。肾脏胶囊可以作为IPCs移植的合适候选人。 (C)2015 Elsevier Ltd.保留所有权利。

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