Hematopoietic stem cells derived from human umbilical cord ameliorate cisplatin-induced acute renal failure in rats.

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2014-09-05 eCollection Date: 2014-01-01
Rokaya H Shalaby, Laila A Rashed, Alaa E Ismaail, Naglaa K Madkour, Sherien H Elwakeel
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Abstract

Injury to a target organ can be sensed by bone marrow stem cells that migrate to the site of damage, undergo differentiation, and promote structural and functional repair. This remarkable stem cell capacity prompted an investigation of the potential of mesenchymal and hematopoietic stem cells to cure acute renal failure. On the basis of the recent demonstration that hematopoietic stem cells (HSCs) can differentiate into renal cells, the current study tested the hypothesis that HSCs can contribute to the regeneration of renal tubular epithelial cells after renal injury. HSCs from human umbilical cord blood which isolated and purified by magnetic activated cell sorting were transplanted intraperitoneal into acute renal failure (ARF) rats which was established by a single dose of cisplatin 5 mg/kg for five days. The Study was carried on 48 male white albino rats, of average weight 120-150 gm. The animals were divided into 4 groups, Group one Served as control and received normal saline throughout the experiments. Group two (model control) received a single dose of cisplatin. Group three and four male-albino rats with induced ARF received interapritoneally (HSCs) at two week and four week respectively. Injection of a single dose of cisplatin resulted in a significant increase in serum creatinine and urea levels, histo-pathological examination of kidney tissue from cisplatin showed severe nephrotoxicity in which 50-75% of glomeruli and renal tubules exhibited massive degenerative change. Four weeks after HSC transplantation, Serum creatinine and urea nitrogen decreased 3.5 times and 2.1 times as well as HGF, IGF-1, VEGF and P53 using quantitative real-time PCR increased 4.3 times, 3.2, 2.4 and 4.2 times compared to ARF groups, respectively. The proliferation of cell nuclear antigen (PCNA)-positive cells (500.083±35.167) was higher than that in the cisplatin groups (58.612±15.743). In addition, the transplanted umbilical cord hematopoietic stem cells UC-HSCs could reside in local injury sites, leading to the relief of hyperemia and inflammation, but no obvious transdifferentiation into renal-like cells. The results lay the foundation for further study on the potential application of UC-HSCs in human disease and Because of their availability; HSC may be useful for cell replacement therapy of acute renal failure.

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源自人类脐带的造血干细胞可改善顺铂诱发的大鼠急性肾衰竭。
骨髓干细胞可感知目标器官的损伤,并迁移到损伤部位,进行分化,促进结构和功能修复。干细胞的这种非凡能力促使人们研究间充质干细胞和造血干细胞治疗急性肾衰竭的潜力。在最近证明造血干细胞可分化为肾脏细胞的基础上,本研究对造血干细胞可促进肾损伤后肾小管上皮细胞再生的假设进行了测试。研究人员将通过磁活化细胞分拣技术分离纯化的人脐带血造血干细胞腹腔移植到急性肾衰竭(ARF)大鼠体内。研究对象为 48 只雄性白化大鼠,平均体重 120-150 克。动物被分为 4 组,第一组作为对照组,在整个实验过程中接受生理盐水。第二组(模型对照组)接受单剂量顺铂。第三组和第四组为诱发 ARF 的雄性纯合子大鼠,分别在两周和四周时接受腹腔注射(造血干细胞)。注射单剂量顺铂后,大鼠血清肌酐和尿素水平显著升高,顺铂肾组织病理学检查显示,50%-75%的肾小球和肾小管出现大量退行性病变,肾毒性严重。移植造血干细胞四周后,血清肌酐和尿素氮分别下降了3.5倍和2.1倍,HGF、IGF-1、VEGF和P53的实时定量PCR检测结果分别是ARF组的4.3倍、3.2倍、2.4倍和4.2倍。细胞核抗原(PCNA)阳性细胞的增殖(500.083±35.167)高于顺铂组(58.612±15.743)。此外,移植的脐带造血干细胞UC-HSCs可驻留在局部损伤部位,使充血和炎症得到缓解,但无明显的肾样细胞转分化。这些结果为进一步研究脐带造血干细胞在人类疾病中的潜在应用奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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