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雷公藤甲素可提高移植到大鼠心肌中的间充质干细胞的早期存活率。

Triptolide improves early survival of mesenchymal stem cells transplanted into rat myocardium.

作者信息

Zhang Changhai, Nong Yaoming, Tong Shifei, Yao Qing, Wen Lei, Zhang Zhihui, Wei Lu, Cheng Jun, Feng Yuanyuan, Song Zhiyuan

机构信息

Department of Cardiology, Southwest Hospital, Third Military Medical University, Chongqing, PR China.

出版信息

Cardiology. 2014;128(2):73-85. doi: 10.1159/000356551. Epub 2014 Feb 18.

DOI:10.1159/000356551
PMID:24557329
Abstract

OBJECTIVE

To investigate whether triptolide can prolong the survival of rat mesenchymal stem cells (MSCs) transfected with the mouse hyperpolarization-activated cyclic nucleotide-gated channel 4 (mHCN4) gene in the myocardium.

METHODS

Grafted cell survival was determined using a sex-mismatched cell transplantation model and analysis of Y chromosome-specific Sry gene expression from hearts harvested at different time points after cell transplantation. ELISA and RT-PCR were used to measure protein and mRNA levels, respectively, of nuclear factor (NF)-κB, IL-1β, IL-6 and TNF-α.

RESULTS

Donor cell numbers decreased over time. Pretreatment with triptolide improved graft survival both 24 (29.3 ± 0.9%) and 72 h (17.5 ± 1.2%) after transplantation of MSCs and resulted in a 2.5-fold increase in the total cell number 72 h after cell transplantation. The mRNA expression and protein content of NF-κB, IL-1β, IL-6 and TNF-α were significantly reduced in the triptolide-treated group compared with the control groups. In addition, triptolide downregulated Bax but upregulated Bcl-2 in the injected region.

CONCLUSIONS

Transient treatment with triptolide may significantly improve the early survival of MSCs in vivo. The mechanism underlying this effect involves attenuating the inflammatory response via inhibition of the NF-κB signaling pathway.

摘要

目的

研究雷公藤甲素是否能延长转染小鼠超极化激活环核苷酸门控通道4(mHCN4)基因的大鼠间充质干细胞(MSCs)在心肌中的存活时间。

方法

采用性别不匹配的细胞移植模型,并分析细胞移植后不同时间点采集的心脏中Y染色体特异性Sry基因表达,以确定移植细胞的存活情况。分别使用ELISA和RT-PCR检测核因子(NF)-κB、白细胞介素-1β(IL-1β)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的蛋白质和mRNA水平。

结果

供体细胞数量随时间减少。雷公藤甲素预处理可提高MSCs移植后24小时(29.3±0.9%)和72小时(17.5±1.2%)的移植物存活率,并使细胞移植后72小时的总细胞数增加2.5倍。与对照组相比,雷公藤甲素治疗组中NF-κB、IL-1β、IL-6和TNF-α的mRNA表达和蛋白质含量显著降低。此外,雷公藤甲素在注射区域下调Bax但上调Bcl-2。

结论

雷公藤甲素短暂治疗可能显著提高体内MSCs的早期存活率。这种作用的潜在机制包括通过抑制NF-κB信号通路减轻炎症反应。

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Triptolide improves early survival of mesenchymal stem cells transplanted into rat myocardium.雷公藤甲素可提高移植到大鼠心肌中的间充质干细胞的早期存活率。
Cardiology. 2014;128(2):73-85. doi: 10.1159/000356551. Epub 2014 Feb 18.
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Triptolide suppresses interleukin-1beta-induced human beta-defensin-2 mRNA expression through inhibition of transcriptional activation of NF-kappaB in A549 cells.雷公藤甲素通过抑制A549细胞中NF-κB的转录激活来抑制白细胞介素-1β诱导的人β-防御素-2 mRNA表达。
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The suppressive effect of triptolide on chronic colitis and TNF-alpha/TNFR2 signal pathway in interleukin-10 deficient mice.雷公藤甲素对白介素-10缺陷小鼠慢性结肠炎及TNF-α/TNFR2信号通路的抑制作用
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Triptolide inhibits tumor promoter-induced uPAR expression via blocking NF-kappaB signaling in human gastric AGS cells.雷公藤甲素通过阻断人胃AGS细胞中的核因子-κB信号通路抑制肿瘤启动子诱导的尿激酶型纤溶酶原激活物受体(uPAR)表达。
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Triptolide impairs dendritic cell migration by inhibiting CCR7 and COX-2 expression through PI3-K/Akt and NF-kappaB pathways.雷公藤甲素通过PI3-K/Akt和NF-κB途径抑制CCR7和COX-2表达,从而损害树突状细胞迁移。
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Triptolide ameliorates autoimmune diabetes and prolongs islet graft survival in nonobese diabetic mice.雷公藤内酯醇改善自身免疫性糖尿病并延长非肥胖型糖尿病小鼠胰岛移植物的存活。
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[Effect of triptolide on airway smooth muscle proliferation and the expression of nuclear factor-kappa B, Bcl-2 in asthmatic rats].雷公藤甲素对哮喘大鼠气道平滑肌增殖及核因子-κB、Bcl-2表达的影响
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Protective effects of triptolide on TLR4 mediated autoimmune and inflammatory response induced myocardial fibrosis in diabetic cardiomyopathy.雷公藤甲素对糖尿病心肌病中Toll样受体4介导的自身免疫和炎症反应诱导的心肌纤维化的保护作用。
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