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人源牙髓间充质基质细胞通过缺血再灌注损伤触发的内分泌机制缓解急性和慢性肾损伤。

The alleviation of acute and chronic kidney injury by human Wharton's jelly-derived mesenchymal stromal cells triggered by ischemia-reperfusion injury via an endocrine mechanism.

机构信息

Department of Urology, Shanghai Jiaotong University School of Medicine, Shanghai, PR China

出版信息

Cytotherapy. 2012 Nov;14(10):1215-27. doi: 10.3109/14653249.2012.711471. Epub 2012 Aug 27.

Abstract

BACKGROUND AIMS

The effects of human Wharton's jelly-derived mesenchymal stromal cells (WJ-MSC) on acute and chronic kidney injury induced by ischemia-reperfusion injury (IRI) were assessed.

METHODS

WJ-MSC were injected intravenously immediately after solitary kidney ischemia for 45 min. Cells were labeled with 5-bromo-2'deoxy-uridine (BrdU) for tracing in vivo. At 48 h post-IRI, serum creatinine and blood urea nitrogen (BUN) were measured. Tubular cell proliferation and apoptosis as well as activation of the Akt signal were identified by immunostaining. Real-time polymerase chain reaction (PCR) was employed to determine gene expression of inflammation-related cytokines and hepatocyte growth factor (HGF). Levels of human HGF were assayed by enzyme-linked immunosorbant assay (ELISA). Twenty-two weeks later, renal fibrosis was assessed by Masson's tri-chrome staining, collagen content and α-smooth muscle actin (α-SMA) staining.

RESULTS

There was no sign of labeled cells residing in the damaged kidney. Acute renal dysfunction elicited by IRI was considerably improved by WJ-MSC, in parallel with a stronger proliferative response and less apoptotic events. Additionally, phosphoAkt staining in injured tubular cells was substantially intensified. Cell treatment also caused a remarkable up-regulation of kidney interleukin (IL)-10, heme oxygenase (HO)-1 and HGF expression. Human HGF was detected in cell supernatants and the serum of cell-infused rats. Moreover, IRI-initiated fibrosis was abrogated by cell therapy, coincident with function amelioration.

CONCLUSIONS

WJ-MSC alleviate acute kidney injury, thereby rescuing the ensuing fibrotic lesions in an endocrine manner. The Akt signal in impaired tubular cells is reinforced by WJ-MSC, facilitating cell resistance to apoptosis and cell proliferation. HGF, either delivered or induced by WJ-MSC, is an important contributor.

摘要

背景目的

评估人沃顿氏胶来源间充质基质细胞(WJ-MSC)对缺血再灌注损伤(IRI)引起的急性和慢性肾损伤的影响。

方法

在单肾缺血 45 分钟后立即静脉注射 WJ-MSC。用 5-溴-2'-脱氧尿苷(BrdU)标记细胞进行体内示踪。在 IRI 后 48 小时,测量血清肌酐和血尿素氮(BUN)。通过免疫染色鉴定肾小管细胞增殖和凋亡以及 Akt 信号的激活。实时聚合酶链反应(PCR)用于确定炎症相关细胞因子和肝细胞生长因子(HGF)的基因表达。通过酶联免疫吸附试验(ELISA)测定人 HGF 的水平。22 周后,通过 Masson 三色染色、胶原含量和α-平滑肌肌动蛋白(α-SMA)染色评估肾纤维化。

结果

没有标记细胞在受损肾脏中存在的迹象。IRI 引起的急性肾功能障碍通过 WJ-MSC 得到显著改善,同时增殖反应增强,凋亡事件减少。此外,受损肾小管细胞中的磷酸化 Akt 染色明显增强。细胞治疗还导致肾脏白细胞介素(IL)-10、血红素加氧酶(HO)-1 和 HGF 的表达显著上调。在细胞上清液和细胞输注大鼠的血清中检测到人 HGF。此外,细胞治疗消除了 IRI 引发的纤维化,同时改善了肾功能。

结论

WJ-MSC 减轻急性肾损伤,从而以内分泌方式挽救随后的纤维化病变。WJ-MSC 增强受损肾小管细胞中的 Akt 信号,促进细胞抵抗凋亡和增殖。HGF 无论是由 WJ-MSC 提供还是诱导,都是一个重要的贡献者。

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