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[骨髓间充质干细胞移植治疗急性心肌梗死:多模态分子成像的体内示踪]

[Bone mesenchymal stem cell transplantation for acute myocardial infarction: in vivo tracing with multi-modality molecular imaging].

作者信息

Chen Hui-zhu, Xia Rui, Guo Ying-kun, Hou Jiang-long, Li Zhen-lin, Ai Hua, Ning Gang, Gao Fa-bao

机构信息

Department of Radiology, West China Second University Hospital, Sichuan University, Chengdu, China.

出版信息

Sichuan Da Xue Xue Bao Yi Xue Ban. 2014 Nov;45(6):898-902.


DOI:
PMID:25571711
Abstract

OBJECTIVE: To investigate the feasibility of tracking bone mesenchymal stem cell (BMSCs) dual- labeled with polyethylenimine 2k-superparamagnetic iron oxide (PEI2k-SPIO) and Luciferase transplantation for acute myocardial infarction in vivo by using magnetic resonance imaging (MRI) and fluorescence imaging. METHODS: BMSCs/Luciferase was incubated with culture medium containing PEI2k-SPIO for 24 h. Prussian-blue staining and MTT were used to assess the efficacy and safety of labeling with PEI2k-SPIO. Guided with echocardiography, the dual-labeled BMSCs were injected into the margin of infarction myocardium. MRI and fluorescence imaging were performed to monitor the cells in vivo at different times (1,2,3,7 d). RESULTS: As demonstrated by MTT, there was no significant difference in survival rate between the labeled and unlabeled cells (P>0. 05). Within a week after transplantation, all PEI2k-SPIO-labeled BMSCs showed a significant decreased signal on MRI. Dual-labeled BMSCs were detected bioluminescence with fluorescence imaging, but disappeared after one week. CONCLUSION: Multi- modality imaging can not only trace the location of labeled BMSCs but also demonstrate the survival of labeled BMSCs in vivo.

摘要

目的:探讨使用磁共振成像(MRI)和荧光成像技术追踪经聚乙烯亚胺2k-超顺磁性氧化铁(PEI2k-SPIO)和荧光素酶双重标记的骨髓间充质干细胞(BMSCs)移植治疗急性心肌梗死的可行性。 方法:将BMSCs/荧光素酶与含PEI2k-SPIO的培养基孵育24小时。采用普鲁士蓝染色和MTT法评估PEI2k-SPIO标记的有效性和安全性。在超声心动图引导下,将双重标记的BMSCs注入梗死心肌边缘。在不同时间点(1、2、3、7天)进行MRI和荧光成像以监测体内细胞。 结果:MTT结果显示,标记细胞与未标记细胞的存活率无显著差异(P>0.05)。移植后一周内,所有PEI2k-SPIO标记的BMSCs在MRI上信号显著降低。双重标记的BMSCs在荧光成像中可检测到生物发光,但一周后消失。 结论:多模态成像不仅可以追踪标记的BMSCs的位置,还可以证明标记的BMSCs在体内的存活情况。

相似文献

[1]
[Bone mesenchymal stem cell transplantation for acute myocardial infarction: in vivo tracing with multi-modality molecular imaging].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2014-11

[2]
In vivo and in vitro imaging tracing of dual-labeled bone mesenchymal stem cells transplanted into myocardium of F344 rats.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2012-10

[3]
[MR imaging of polyethylenimine-superparamagnetic iron oxide nanoparticle labeled bone marrow mesenchymal stem cells in vitro].

Sichuan Da Xue Xue Bao Yi Xue Ban. 2012-7

[4]
In vivo tracing of superparamagnetic iron oxide-labeled bone marrow mesenchymal stem cells transplanted for traumatic brain injury by susceptibility weighted imaging in a rat model.

Chin J Traumatol. 2010-6-1

[5]
[In vivo tracking of bone marrow mesenchymal stem cells labeled with superparamagnetic iron oxide after cerebral ischemia in rats by magnetic resonance imaging].

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2007-2

[6]
In vivo magnetic resonance imaging tracking of transplanted superparamagnetic iron oxide-labeled bone marrow mesenchymal stem cells in rats with myocardial infarction.

Mol Med Rep. 2015-1

[7]
Dual-modular molecular imaging to trace transplanted bone mesenchymal stromal cells in an acute myocardial infarction model.

Cytotherapy. 2015-10

[8]
Superparamagnetic iron oxide magnetic nanomaterial-labeled bone marrow mesenchymal stem cells for rat liver repair after hepatectomy.

J Surg Res. 2014-3-27

[9]
MR tracking of SPIO-labeled mesenchymal stem cells in rats with liver fibrosis could not monitor the cells accurately.

Contrast Media Mol Imaging. 2015

[10]
Treatment of rat with traumatic brain injury and MR tracing in vivo via combined transplantation of bone marrow stromal cells labeled with superparamagnetic iron oxide and Schwann cells.

J Biomed Nanotechnol. 2014-2

引用本文的文献

[1]
Bone marrow mesenchymal stromal cells with CD47 high expression via the signal transducer and activators of transcription signaling pathway preventing myocardial fibrosis.

Int J Clin Exp Pathol. 2015-9-1

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