Summary

Мультимодальные изображений имплантации стволовых клеток в центральной нервной системе мышей

Published: June 13, 2012
doi:

Summary

В этой статье описываются оптимизированные последовательности событий для мультимодальных изображений клеточных трансплантатов у грызунов мозга с помощью: (I) в естественных условиях биолюминесценции и магнитно-резонансной томографии, и (II) после смерти гистологический анализ. Сочетание этих условий изображение на одного животного позволяет сотовой трансплантата оценки с высоким разрешением, чувствительностью и специфичностью.

Abstract

During the past decade, stem cell transplantation has gained increasing interest as primary or secondary therapeutic modality for a variety of diseases, both in preclinical and clinical studies. However, to date results regarding functional outcome and/or tissue regeneration following stem cell transplantation are quite diverse. Generally, a clinical benefit is observed without profound understanding of the underlying mechanism(s)1. Therefore, multiple efforts have led to the development of different molecular imaging modalities to monitor stem cell grafting with the ultimate aim to accurately evaluate survival, fate and physiology of grafted stem cells and/or their micro-environment. Changes observed in one or more parameters determined by molecular imaging might be related to the observed clinical effect. In this context, our studies focus on the combined use of bioluminescence imaging (BLI), magnetic resonance imaging (MRI) and histological analysis to evaluate stem cell grafting.

BLI is commonly used to non-invasively perform cell tracking and monitor cell survival in time following transplantation2-7, based on a biochemical reaction where cells expressing the Luciferase-reporter gene are able to emit light following interaction with its substrate (e.g. D-luciferin)8, 9. MRI on the other hand is a non-invasive technique which is clinically applicable10 and can be used to precisely locate cellular grafts with very high resolution11-15, although its sensitivity highly depends on the contrast generated after cell labeling with an MRI contrast agent. Finally, post-mortem histological analysis is the method of choice to validate research results obtained with non-invasive techniques with highest resolution and sensitivity. Moreover end-point histological analysis allows us to perform detailed phenotypic analysis of grafted cells and/or the surrounding tissue, based on the use of fluorescent reporter proteins and/or direct cell labeling with specific antibodies.

In summary, we here visually demonstrate the complementarities of BLI, MRI and histology to unravel different stem cell- and/or environment-associated characteristics following stem cell grafting in the CNS of mice. As an example, bone marrow-derived stromal cells, genetically engineered to express the enhanced Green Fluorescent Protein (eGFP) and firefly Luciferase (fLuc), and labeled with blue fluorescent micron-sized iron oxide particles (MPIOs), will be grafted in the CNS of immune-competent mice and outcome will be monitored by BLI, MRI and histology (Figure 1).

Protocol

1. Сотовые подготовка Эксперимент следует начать использование бывших естественных культурных стволовых клеточных популяций генетически модифицированных выразить люциферазы и белков EGFP репортера. Здесь мы используем люциферазы / EGFP экспрессией мышиных костномозгового происх…

Discussion

В этом докладе мы описываем оптимизированный протокол для комбинации из трех дополнительных методов визуализации (BLI, МРТ и гистология) подробные характеристики клеточных имплантантов в ЦНС иммунокомпетентных мышей. Сочетание гена-репортера маркировки клеток, основанный на генетиче…

Divulgations

The authors have nothing to disclose.

Acknowledgements

<p class="jove_content"> Авторы Работа выполнена при поддержке исследовательского гранта ID-конвертерного 2006 году в Университете Антверпена (предоставляется РРО и AVDL), на исследовательский грант G.0136.11 и G.0130.11 (предоставляется AVDL, ZB и ППО) и 1.5.021.09. N.00 (предоставляется РРО) Фонда научных исследований, Фландрии (FWO-Vlaanderen, Бельгия), по SBO грант ИВТ-60838: BRAINSTIM из Фламандского института по науке и технике (предоставляется ZB и AVDL), в частично Methusalem исследовательский грант от правительства Фландрии (предоставляется ZB), в частности, ИС-FP6-NoE Дими (LSHB-CT-2005-512146), EC-FP6-NoE EMIL (LSHC-CT-2004-503569) , а Интер университета Привлечение поляков IUAP-NIMI-P6/38 (предоставляется AVDL). Натали Де Vocht степень доктора наук, стипендия от FWO-Vlaanderen. Петр Ponsaerts это после защиты докторской диссертации в FWO-Vlaanderen.</p>

Materials

Name of the reagent Company Catalogue number Comments
IMDM Lonza BE12-722F Component of the cell growth medium CEM
Fetal bovine serum Gibco 10270-106 Component of the cell growth medium CEM
Horse serum Gibco 1605-122 Component of the cell growth medium CEM
Penicillin-streptomycin Gibco 15140 Component of the cell growth medium CEM
Fungizone Gibco 15290-018 Component of the cell growth medium CEM
PBS Gibco 14190  
Puromycine Invivogen ant-pr-1  
trypsin Gibco 25300  
GB MPIO Bangs Laboratories ME04F/7833  
D-luciferin Promega E1601  
Ketamine (Ketalar) Pfizer    
Xylazine (Rompun) Bayer Health care    
Isoflurane Isoflo 05260-05  
0.9% NaCl solution Baxter    
paraformaldehyde Merck 1.04005.1000  
sucrose Applichem A1125  
Micro-injection pump KD scientific KDS100  
Photon imager Biospace Lab    
9.4T MR scanner Bruker Biospin Biospec 94/20 USR  
BX51 microscope Olympus BX51  
Mycrom HM cryostat Prosan HM525  
syringe Hamilton 7635-01  
30 gauge needle Hamilton 7762-03  
Photo Vision software Biospace Lab    
M3vision software Biospace Lab    
Paravision 5.1 software Bruker Biospin    
Amira 4.0 software Visage Imaging    

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De Vocht, N., Reekmans, K., Bergwerf, I., Praet, J., Hoornaert, C., Le Blon, D., Daans, J., Berneman, Z., Van der Linden, A., Ponsaerts, P. Multimodal Imaging of Stem Cell Implantation in the Central Nervous System of Mice. J. Vis. Exp. (64), e3906, doi:10.3791/3906 (2012).

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