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磁共振示踪磁标记骨髓间充质干细胞在肝纤维化大鼠中的研究。

MR tracking of magnetically labeled mesenchymal stem cells in rats with liver fibrosis.

机构信息

Department of Radiology, Third Affiliated Hospital of Sun Yat-sen University, Guangzhou 510630, China.

出版信息

Magn Reson Imaging. 2010 Apr;28(3):394-9. doi: 10.1016/j.mri.2009.12.005. Epub 2010 Jan 21.


DOI:10.1016/j.mri.2009.12.005
PMID:20096523
Abstract

PURPOSE: In vivo magnetic resonance (MR) tracking of magnetically labeled bone marrow mesenchymal stem cells (BMSCs) administered via the mesenteric vein to rats with liver fibrosis. MATERIALS AND METHODS: Rat BMSCs were labeled with superparamagnetic iron oxide (SPIO) and the characteristics of the BMSCs after labeling were investigated. Eighteen rats with CCL4-induced liver fibrosis were randomized to three groups to receive SPIO-labeled BMSCs (BMSC-labeled group), cell-free SPIO (SPIO group), or unlabeled BMSCs (control group). MR imaging of the liver was performed at different time points, and signal-to-noise ratio (SNR) of the liver was measured. In vivo distribution of delivered BMSCs was assessed by histological analysis. RESULTS: Labeling of BMSCs with SPIO did not significantly alter cell viability and proliferation activity. In BMSC-labeled group, the liver SNR immediately decreased from 8.56+/-0.26 to 3.53+/-0.41 at 1 h post injection and remained at a significantly lower level till 12 days (P<.05 versus the level before). By contrast, the liver SNR of the SPIO group almost recovered to the preinjection level (P=.125) at 3 days after a transient decrease. In control group, the liver SNR demonstrated no significant difference at the tested time points. Additionally, Prussian blue-positive cells were mainly distributed in the liver parenchyma, especially in injured areas. CONCLUSION: The magnetically labeled BMSCs infused through the mesenteric vein can be detected in the fibrotic liver of rats using in vivo MR imaging up to 12 days after injection.

摘要

目的:经肠系膜静脉向肝纤维化大鼠体内输注磁性标记骨髓间充质干细胞(BMSCs),并进行活体磁共振(MR)追踪。

材料与方法:将超顺磁氧化铁(SPIO)标记大鼠 BMSCs,观察标记后 BMSCs 的特性。将 18 只 CCL4 诱导的肝纤维化大鼠随机分为 3 组,分别接受 SPIO 标记的 BMSCs(BMSC 标记组)、无细胞 SPIO(SPIO 组)或未标记的 BMSCs(对照组)。分别于不同时间点行肝脏 MR 成像,测量肝脏的信噪比(SNR)。采用组织学分析评估移植 BMSCs 的体内分布。

结果:SPIO 标记 BMSCs 不显著改变细胞活力和增殖活性。BMSC 标记组,肝 SNR 于注射后 1 h 即刻从 8.56±0.26 降至 3.53±0.41,且在 12 天内一直维持在显著较低水平(P<0.05 与注射前水平相比)。相比之下,SPIO 组的肝 SNR 在短暂降低后于 3 天几乎恢复到注射前水平(P=.125)。对照组在测试时间点的肝 SNR 无显著差异。此外,普鲁士蓝阳性细胞主要分布在肝实质内,尤其是在损伤区域。

结论:经肠系膜静脉输注的磁性标记 BMSCs 可在注射后 12 天内通过活体 MR 成像在大鼠纤维化肝脏中检测到。

相似文献

[1]
MR tracking of magnetically labeled mesenchymal stem cells in rats with liver fibrosis.

Magn Reson Imaging. 2010-1-21

[2]
MR tracking of SPIO-labeled mesenchymal stem cells in rats with liver fibrosis could not monitor the cells accurately.

Contrast Media Mol Imaging. 2015

[3]
In vivo MR imaging of magnetically labeled mesenchymal stem cells transplanted into rat liver through hepatic arterial injection.

Contrast Media Mol Imaging. 2008

[4]
[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

[5]
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

[6]
Superparamagnetic iron oxide magnetic nanomaterial-labeled bone marrow mesenchymal stem cells for rat liver repair after hepatectomy.

J Surg Res. 2014-3-27

[7]
In vivo MR imaging of intravascularly injected magnetically labeled mesenchymal stem cells in rat kidney and liver.

Radiology. 2004-12

[8]
In vivo magnetic resonance imaging of iron oxide-labeled, arterially-injected mesenchymal stem cells in kidneys of rats with acute ischemic kidney injury: detection and monitoring at 3T.

J Magn Reson Imaging. 2007-6

[9]
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Asian J Androl. 2007-5

[10]
Transplantation of MSCs Overexpressing HGF into a Rat Model of Liver Fibrosis.

Mol Imaging Biol. 2016-2

引用本文的文献

[1]
Tracking of Stem Cells in Chronic Liver Diseases: Current Trends and Developments.

Stem Cell Rev Rep. 2024-2

[2]
Magnetic Nanostructures and Stem Cells for Regenerative Medicine, Application in Liver Diseases.

Int J Mol Sci. 2023-5-26

[3]
Bone Marrow-Derived Mesenchymal Stem Cell Potential Regression of Dysplasia Associating Experimental Liver Fibrosis in Albino Rats.

Biomed Res Int. 2019-11-6

[4]
Mesenchymal stem cell transplantation improves chronic colitis-associated complications through inhibiting the activity of toll-like receptor-4 in mice.

BMC Gastroenterol. 2018-8-13

[5]
Homing and Tracking of Iron Oxide Labelled Mesenchymal Stem Cells After Infusion in Traumatic Brain Injury Mice: a Longitudinal In Vivo MRI Study.

Stem Cell Rev Rep. 2018-12

[6]
Noninvasive in-vivo tracing and imaging of transplanted stem cells for liver regeneration.

Stem Cell Res Ther. 2016-9-23

[7]
Probe-Based Confocal Laser Endomicroscopy for Imaging TRAIL-Expressing Mesenchymal Stem Cells to Monitor Colon Xenograft Tumors In Vivo.

PLoS One. 2016-9-12

[8]
Transplantation of MSCs Overexpressing HGF into a Rat Model of Liver Fibrosis.

Mol Imaging Biol. 2016-2

[9]
Effects of bone marrow-derived mesenchymal stem cells transplanted via the portal vein or tail vein on liver injury in rats with liver cirrhosis.

Exp Ther Med. 2015-4

[10]
Optimization of mesenchymal stem cells (MSCs) delivery dose and route in mice with acute liver injury by bioluminescence imaging.

Mol Imaging Biol. 2015-4

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