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Method Article

In Vivo Study of Human Endothelial-Pericyte Interaction Using the Matrix Gel Plug Assay in Mouse

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DOI:

10.3791/54617

December 19th, 2016

In This Article

Summary

We present a protocol to study human endothelial-pericyte interactions in mouse using a variation of the matrix gel plug angiogenesis assay.

Abstract

Angiogenesis is the process by which new blood vessels are formed from existing vessels. New vessel growth requires coordinated endothelial cell proliferation, migration, and alignment to form tubular structures followed by recruitment of pericytes to provide mural support and facilitate vessel maturation. Current in vitro cell culture approaches cannot fully reproduce the complex biological environment where endothelial cells and pericytes interact to produce functional vessels. We present a novel application of the in vivo matrix gel plug assay to study endothelial-pericyte interactions and formation of functional blood vessels using severe combined immune deficiency mutation (SCID) mice. Briefly, matrix gel is mixed with a solution containing endothelial cells with or without pericytes followed by injection into the back of anesthetized SCID mice. After 14 days, the matrix gel plugs are removed, fixed and sectioned for histological analysis. The length, number, size and extent of pericyte coverage of mature vessels (defined by the presence of red blood cells in the lumen) can be quantified and compared between experimental groups using commercial statistical platforms. Beyond its use as an angiogenesis assay, this matrix gel plug assay can be used to conduct genetic studies and as a platform for drug discovery. In conclusion, this protocol will allow researchers to complement available in vitro assays for the study of endothelial-pericyte interactions and their relevance to either systemic or pulmonary angiogenesis.

Introduction

Angiogenesis is the process by which new blood vessels are formed from a pre-existing vascular network1 and is the focus of ongoing research across many areas ranging from normal development to disease. This dynamic process involves the proliferation and migration of endothelial cells (ECs) and recruitment of pericytes to construct a vascular tube that is directed toward the site that needs oxygen and nutrient delivery2. To study this process requires an equally dynamic assay, most importantly one that can recapitulate the three-dimensional nature of tube formation. In vitro 3D matrix assays have been developed to address this need and h....

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Protocol

Ethics Statement: Procedures involving animal subjects have been approved by the Institutional Animal Care and Use Committee at Stanford University School of Medicine.

NOTE: Animals are under anesthetization with 3% vaporizer isoflurane and 3% supply of O2 gas. Use of vet ointment on eyes may help to prevent dryness while under anesthesia.

1. Cell Preparation

  1. Grow human endothelial and pericyte cell cultures in 100 mm plates with 10 ml of the appropriate media. Replace 10 ml of fresh medium every 2 - 3 days until cells reach 80% confluency.
    1. Culture endothelial cells (ECs) in complete endothelial cell media (ECM) supplem....

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Results

Representative H&E and immunofluorescent staining of matrix gel plug sections are shown in Figure 2. Sections from EC only plugs display some vessels that are mostly not perfused with blood (Figure 2 top left, black arrows) whereas plugs containing both ECs and pericytes display several perfused vessels with larger diameters and complete pericyte coverage, as evidenced by positive SMA staining immediately adjacent to CD31-positive ECs. These results s.......

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Discussion

The matrix gel plug assay has proven to be a convenient and powerful method to evaluate gene regulation in angiogenesis, angiogenic and antiangiogenic compounds in vivo, and to supplement in vitro tests. Here, we describe in detail a novel matrix gel plug assay of human angiogenesis that investigates the interaction between endothelial cells and pericytes during vessel formation.

There are a few novel and critical steps in this protocol. Cells in low passage (passage 1 - 4) a.......

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Disclosures

No competing financial interests enclosed.

Acknowledgements

Dr. K. Yuan was supported by an American Heart Association Scientist Development Grant (15SDG25710448) and the Pulmonary Hypertension Association Proof of Concept Award (SPO121940). Dr. V. de Jesus Perez was supported by a career development award from the Robert Wood Johnson Foundation, an NIH K08 HL105884-01 award, a Pulmonary Hypertension Association Award, a Biomedical Research Award from the American Lung Association and a Translational Research and Applied Medicine award from Stanford University.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
PBS (Phosphate buffered saline)Corning21-031-CV
0.25% Trypsin/0.53 mM EDTACorning25-053-CI
Endothelial Cell Media (ECM) kitSciencell1001includes media, EC growth supplement, and penicillin/streptomycin, each supplied at the appropriate volume for easy mixing
Pericyte Media (PM) kitSciencell1201includes media, Pericyte growth supplement, and penicillin/streptomycin, each supplied at the appropriate volume for easy mixing
primary human pulmonary microvascular endothelial cellsPulmonary Hypertension Breakthrough Initiativethis cell type is also available commercially. Cells used at passage 1-4
primary human pulmonary pericytesPulmonary Hypertension Breakthrough Initiativethis cell type is not available commercially, but brain paricytes are.  Cells used at passage 1-4
bFGF (basic Fibroblast Growth Factor)Peprotech100-18Bstock solution is 50 μg/ml in 0.1% BSA in PBS, aliquots at 50 μl and stored at -20 degrees
Matrigel Basement Membrane MatrixBD356237
28 G 1 cc Insluin SyringeBD329410
SCID (Severe Combined Immune Deficiency) miceThe Jackson Laboratory5557NOD.SCID IL2R gamma knockout strain is the best strain; 4-6 weeks of age
1.5 ml microcentrifuge tubes, sterileThermo Fisher Scientific05-408-129
15 ml screw top tubes, sterileBD Biosciences352096
PAP penLife Technologies8899
hemocytometerThermoFisher Scientific02-671-6
Nair hair removal creamWalmart
anti-human CD31 primary antibodyLifeSpan BiosciencesLS-B4737working solution is 1:50
anti-human Smooth Muscle actin CY3 primary fluorescent antibodySigmaC6198working solution is 1:300
goat anti-rabbit secondary antibody; 488/greenThermoFisher ScientificA-11008working solution is 1:250
Prolong Gold DAPI solutionCell Signaling8961S
microscope slidesVWR48300-047
no. 1.5 cover slipsThermo Fisher Scientific12-544-D
citrate buffer 10xMillipore21545
extra fine surgical scissorsFine Science Tools14084-08
Formalin (paraformaldehyde)Thermo Fisher Scientific245-685
Tissue cassettesSimportM492-12
goat serumDakoX0907

References

  1. Risau, W. Mechanisms of angiogenesis. Nature. 386 (6626), 671-674 (1997).
  2. Ribatti, D., Nico, B., Crivellato, E. The role of pericytes in angiogenesis. Int J Dev Biol. 55 (3), 261-268 (2011).
  3. Koh, W., Stratman, A. N., Sacharidou, A., Davis, G. E.

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Tags

In Vivo AngiogenesisHuman Endothelial CellsParasite Cell CultureSCID Mice ModelHistological AnalysisPericyte CoverageVessel MaturationBlood Vessel Formation