Skip to main content

The Murine Hindbrain as a Model to Study the Molecular and Cellular Mechanisms of Angiogenesis in Intact Tissues

  • Chapter
  • First Online:

Abstract

This chapter describes methodology to exploit the murine hindbrain as a powerful and versatile model system with three main advantages for studying developmental angiogenesis. Firstly, the hindbrain model permits the accurate assessment of the intricate behaviour of endothelial cells within a natural multicellular microenvironment. Secondly, due to the early embryonic vascularisation of the hindbrain, it is particularly useful to study genetic mutations that result in embryonic lethality, reducing the need to breed conditional knockout mice, as for postnatal models. Thirdly, the unique architecture of the vascular network in this tissue allows high resolution imaging of angiogenic molecules and vascular structures that are readily quantifiable.

An erratum to this chapter can be found at http://dx.doi.org/10.1007/978-94-007-4581-0_26

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   39.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   54.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD   54.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Abbreviations

HRP:

Horseradish peroxidase

IB4:

Isolectin B4

PECAM:

Platelet endothelial cell adhesion molecule

NGS:

Normal goat serum

NRS:

Normal rabbit serum

PBS:

Phosphate buffered saline

PBT:

PBS + 0.1% TritonX100

PFA:

Paraformaldehyde

SVP:

Subventricular vascular plexus

VEGF:

Vascular endothelial growth factor

References

  1. Fantin A, Vieira JM, Gestri G et al (2010) Tissue macrophages act as cellular chaperones for vascular anastomosis downstream of VEGF-mediated endothelial tip cell induction. Blood 116(5):829–840

    Article  PubMed  CAS  Google Scholar 

  2. Ruhrberg C, Gerhardt H, Golding M et al (2002) Spatially restricted patterning cues provided by heparin-binding VEGF-A control blood vessel branching morphogenesis. Genes Dev 16(20):2684–2698

    Article  PubMed  CAS  Google Scholar 

  3. James JM, Gewolb C, Bautch VL (2009) Neurovascular development uses VEGF-A signaling to regulate blood vessel ingression into the neural tube. Development 136(5):833–841

    Article  PubMed  CAS  Google Scholar 

  4. Raab S, Beck H, Gaumann A et al (2004) Impaired brain angiogenesis and neuronal apoptosis induced by conditional homozygous inactivation of vascular endothelial growth factor. Thromb Haemost 91(3):595–605

    PubMed  CAS  Google Scholar 

  5. Haigh JJ, Morelli PI, Gerhardt H et al (2003) Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling. Dev Biol 262(2):225–241

    Article  PubMed  CAS  Google Scholar 

  6. Albelda SM, Muller WA, Buck CA, Newman PJ (1991) Molecular and cellular properties of PECAM-1 (endoCAM/CD31): a novel vascular cell-cell adhesion molecule. J Cell Biol 114(5):1059–1068

    Article  PubMed  CAS  Google Scholar 

  7. Laitinen L (1987) Griffonia simplicifolia lectins bind specifically to endothelial cells and some epithelial cells in mouse tissues. Histochem J 19(4):225–234

    Article  PubMed  CAS  Google Scholar 

  8. Austyn JM, Gordon S (1981) F4/80, a monoclonal antibody directed specifically against the mouse macrophage. Eur J Immunol 11(10):805–815

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgements

We thank Dr Alessandro Fantin for Fig. 1 and critical reading of the manuscript. We are grateful to L. Denti, K. Davidson and the staff of the Biological Resources Unit at the UCL Institute of Ophthalmology for help with mouse husbandry. We gratefully acknowledge the Imaging Facility of the UCL Institute of Ophthalmology for maintenance of the confocal microscopes. C.M. was funded by an MRC doctoral training account (ref. G0601093).

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Christiana Ruhrberg .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2012 Springer Science+Business Media Dordrecht

About this chapter

Cite this chapter

Maden, C., Ruhrberg, C. (2012). The Murine Hindbrain as a Model to Study the Molecular and Cellular Mechanisms of Angiogenesis in Intact Tissues. In: Zudaire, E., Cuttitta, F. (eds) The Textbook of Angiogenesis and Lymphangiogenesis: Methods and Applications. Springer, Dordrecht. https://doi.org/10.1007/978-94-007-4581-0_13

Download citation

Publish with us

Policies and ethics