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W tym Artykule

  • Podsumowanie
  • Streszczenie
  • Wprowadzenie
  • Protokół
  • Wyniki
  • Dyskusje
  • Ujawnienia
  • Podziękowania
  • Materiały
  • Odniesienia
  • Przedruki i uprawnienia

Podsumowanie

Monocytes are important mediators of arteriogenesis in the context of peripheral arterial disease. Using a basement membrane-like matrix and intravital microscopy, this protocol investigates monocyte homing and tumor-related angiogenesis after monocyte injection in the femoral artery ligation murine model.

Streszczenie

The therapeutic goal for peripheral arterial disease and ischemic heart disease is to increase blood flow to ischemic areas caused by hemodynamic stenosis. Vascular surgery is a viable option in selected cases, but for patients without indications for surgery such as progression to rest pain, critical limb ischemia, or major disruptions to life or work, there are few possibilities for mitigating their disease. Cell therapy via monocyte-enhanced perfusion through the stimulation of collateral formation is one of a few non-invasive options.

Our group examines arteriogenesis after monocyte transplantation into mice using the hindlimb ischemia model. Previously, we have demonstrated improvement in hindlimb perfusion using tetanus-stimulated syngeneic monocyte transplantation. In addition to the effects on the collateral formation, tumor growth could be affected by this therapy as well. To investigate these effects, we use a basement membrane-like matrix mouse model by injecting the extracellular matrix of the Engelbreth-Holm-Swarm sarcoma into the flank of the mouse, after occlusion of the femoral artery.

After the artificial tumor studies, we use intravital microscopy to study in vivo tumor-angiogenesis and monocyte homing within collateral arteries. Previous studies have described the histological examination of animal models, which presupposes subsequent analysis to post-mortem artifacts. Our approach visualizes monocyte homing to areas of collateralization in real time sequences, is easy to perform, and investigates the process of arteriogenesis and tumor angiogenesis in vivo.

Wprowadzenie

Cardiovascular diseases, including coronary heart disease or peripheral arterial disease, are the most common causes of death globally1. Cell therapy is a promising approach to treat cardiovascular disease, particularly for people who are not able to undergo surgical interventions. There are several approaches to use cells or their secreted substances as a therapeutic tool2,3, with the overall goal to improve the perfusion and maintain function of ischemic and underperfused tissue. One attempt to achieve this goal is to improve arteriogenesis, which enhances the development of collatera

Protokół

Our study was performed with permission of the state of Saxony-Anhalt, Landesverwaltungsamt Halle, according to section 8 of the German law for animal protection. (§ 8, paragraph 1 of the German law for animal protection from 18.05.2016 - BGBI. I S. 1206, 1313, § 31 TierSchVersV from 13.08.2013).

NOTE: For the experiments here, 8 to 12 week old male BALB/c mice were used, and human monocytes from blood donors were used for the visualization of monocytes via intravital microscopy.

1. Cell Preparation

NOTE: For the isolation of monocytes, please see our previous published

Wyniki

Intravital microscopy for the examination of tumor and collateral vessel growth triggered by monocytes can help reveal new aspects in the molecular mechanisms of tumor angiogenesis and arteriogenesis. Cells must be prepared and injected carefully using the steps of the protocol. Differences can lead to variations between single experiments. The monocytes must be injected into the venous system (Figure 1) to maintain systemic effects and avoid emboli, which ca...

Dyskusje

The method described here sheds light on the development of collateral arteries, the behavior of monocytes in these vessels, and the process of arteriogenesis. The steps for applying this protocol are easy to learn and can be used in other fields of science. Despite these advantages, there are some disadvantages. For instance, microscopic equipment is required to execute the described techniques. Obtaining equipment for one experiment is unsustainable, so it is important to collaborate with other institutions to share th...

Ujawnienia

The authors declare that they have no competing financial interests.

Podziękowania

This work was supported by the ELSE-Kröner-Stiftung and the DFG (Deutsche Forschungsgemeinschaft, German Research Foundation) SFB 854 (Sonderforschungsbereich, collaborative research center). Special thanks to Hans-Holger Gärtner, Audiovisuelles Medienzentrum, Otto-von-Guericke University Magdeburg, Magdeburg, Germany, for technical support.

Materiały

NameCompanyCatalog NumberComments
10% fetal calf serum (FCS)Sigma Aldrich, Hamburg, Germany
1% penicillin/streptomycinSigma Aldrich, Hamburg, Germany
1mL Omnifix -F insuline syringeB. Braun, Melsungen AG, Melsungen, Germany
50 ml syringe Fresenius Kabi AG, Bad Homburg, GermanyInjectomat- syringe 50 ml with canule
6-well-ultra-low-attachement-platesCorning Incorporated, NY, USA
8- 12 week old, male, C57BL/6, BalbC mice Charles River, Sulzfeld, Germany
Adhesive tapeTESA SE, Hamburg, Germany
Acquisition SoftwareLeica, Wetzlar, Deutschland Leica Application Suite Advanced Fluorescence (LAS AF); Version: 2.7.3.9723
CanulesB. Braun, Melsungen AG, Melsungen, Germany29G, 30G
Cell culture dishGreiner Bio-One GmbH, Frickenhausen, Germany
Cell culture mediumManufactured by our group with single componentsMedium199, 10% Fetal calf serum, 1% Antibiotic (penicillin/streptomycin)
CentrifugeBeckman Coulter GmbH, Krefeld, GermanyAllegra X-15R centrifuge
Depilatory creamVeet, Mannheim, Germany
DiOInvitrogen Eugene, Oregon, USA
Disinfection agentSchülke&Mayr GmbH, Norderstedt, Germany
Disposable scalpel No.10 Feather safety razor Co.Ltd, Osaka, Japan 
EDTASigma Aldrich, Hamburg, Germany
Erlenmeyer flaskGVB, Herzogenrath, Germany
Ethanol 70%Otto Fischar GmbH und Co KG, Saarbrücken, Germany
Fetal Calf SerumSigma Aldrich, Hamburg, Germany
Fine ForcepsRubis, Stabio, Switzerland
Flurophor/RhodamindextranThermo Fischer Scientific, Waltham, MA USAKatalognummer: D-1819
GlovesRösner-Matby Meditrade GmbH, Kiefersfelden, Germany
Heating pad Labotect GmbH, Göttingen, Germany Hot Plate 062
Human macrophage-colony stimulating factorSigma Aldrich, Hamburg, GermanySRP3110 
Humane leucocyte filtersBlood preservation
IncubatorEwald Innovationstechnik GmbH, Bad Nenndorf, Germany
IsofluraneBaxter Deutschland GmbH, Unterschleißheim, Germany
Ketamine (10%)Ketavet, Pfizer Deutschland GmbH, Berlin , Germany
Leukocyte separation tubes (tubes with filter) Bio one GmbH, Frickenhausen, Germany
Light microscope Carl Zeiss SMT GmbH, Oberkochen, GermanyAxiovert 40 C
Lymphocyte separation medium LSM1077GE Healthcare, Pasching, Austria
Matrigel Becton, Dickinson and Company, Franklyn Lakes, New Jersey, USA
Medium M199 PAA Laboratories GmbH, Pasching, Austria
Microbiological work benchThermo Electron, LED GmbH, Langenselbold, GermanyHera safe
Microscope slideCarl Roth GmbH + Co. KG, KarlsruheArt. Nr. 1879
Microscope stand with incubator and heating unit Leica DMI 6000, Pecon, Germany
Monocyte wash bufferManufactured by our group with single componentsPBS, 0,5% BSA, 2mM EDTA
Mouse restrainerVarious
Multi-photon microscope Leica, Wetzlar, Deutschland Leica SP5 Confocal microscope, Cameleon, Coherent
NaCl (0,9%)Berlin Chemie AG, Berlin, Germany
Neubauer counting chamber Paul Marienfeld GmbH und Co.KG, Lauda-Königshofen, Germany
ObjectiveLeica, Wetzlar, Deutschland Leica HC PL APO 10x/0.4 CS
PBSLife technologies GmbH, Darmstadt, Germanyph 7,4 sterile
Penicillin/StreptomycinSigma Aldrich, Hamburg, Germany
PercollManufactured by our group with single components90 % Percoll, 10% 1,5M NaCl, ρ= 1,064 g cm-3
Percoll solutionGE Healthcare, Bio-Science AB, Uppsala, Sweden
PipettesEppendorf AG, Hamburg, Germany10µL/100µL/200µL/1000µL
Pipettes serologicalGreiner Bio-One GmbH, Frickenhausen, Germany Cellstar2ml, 5ml, 10ml
Pipetting headsEppendorf AG, Hamburg, Germany
PipetusEppendorf AG, Hamburg, Germany
Polystyrol tubeCellstar, Greiner Bio-One GmbH, Frickenhausen, Germany
ScissorWord Precision Instruments, Inc., Sarasota, USA
ScaleMettler PM4800 Delta Range, Mettler-Toledo GmbH, Gießen, Germany
Suction unitIntegra bioscience, Fernwald, GermanyVacusafe comfort
Surgical scissorsWord Precision Instruments, Inc., Sarasota, USA
Trypan blue solution 0,4 %Sigma Aldrich, Hamburg, Germany
Tubes with capGreiner Bio-One GmbH, Frickenhausen, Germany15ml, 50ml Cellstar
Xylazine (2 %)Ceva Tiergesundheit GmbH, Düsseldorf, Germany

Odniesienia

  1. Volz, K. S., Miljan, E., Khoo, A., Cooke, J. P. Development of pluripotent stem cells for vascular therapy. Vascular pharmacology. 56 (5-6), 288-296 (2012).
  2. Henry, T. D., et al. The VIVA trial: Vascular en

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Keywords Intravital MicroscopyMonocyte HomingTumor related AngiogenesisPeripheral Arterial DiseaseCell LabelingMatrigelVEGFBFGFHeparinSubcutaneous InjectionSystemic Cell Application

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