Skip to main content

Correlative Video-Light–Electron Microscopy of Mobile Organelles

  • Protocol
  • First Online:
Membrane Trafficking

Abstract

Correlative microscopy is a method when for the analysis of the very same cell or tissue area, several different methods of light microscopy (LM) and then electron microscopy (EM) are used consecutively. The combination of LM and EM allows researchers to study phenomena at a global scale and then to look for unique or rare events for their subsequent EM examination. Unfortunately, the observation of living cells under EM is still impossible. LM provides the possibility to examine quickly many live cells, whereas EM provides the high level of resolution. On the other side, the final goal of any morphological analysis of a biological sample, whether it is an organism, organ, tissue, cell, organelle, or molecule, is to get an averaged three-dimensional model of the structure examined and to determine the chemical composition of it. This chapter describes the methodology of imaging with the help of CVLEM. The guidelines presented herein enable researchers to analyze structure of organelles and to obtain the three-dimensional model of the structure examined, and in particular rare events captured by low-resolution imaging of a population or transient events captured by live imaging can now also be studied at high resolution by EM.

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

Access this chapter

Protocol
USD 49.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 139.00
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 109.99
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

Institutional subscriptions

References

  1. Bopp-Hassenkamp G (1958)Lichtmikroskopische und elektronenoptische untersuchungen uber den aufbau pflanzlicher chromosomen im pachytan der meiosis. Protoplasma 2:1–3

    Google Scholar 

  2. Rieder CL, Davison EA, Jensen LC, Cassimeris L, Salmon ED (1986) Oscillatory movements of monooriented chromosomes and their position relative to the spindle pole result from the ejection properties of the aster and half-spindle. J Cell Biol 103(2):581–591

    Article  CAS  PubMed  Google Scholar 

  3. Mironov AA, Mironov VA, Rekhter MD (1987) [Changes in the surface and cytoskeletal apparatus of the endotheliocytes of the rat aorta during division (based on scanning electron microscopic data)]. Tsitologiia 29(4):426–431

    CAS  PubMed  Google Scholar 

  4. Polishchuk RS, Polishchuk EV, Marra P, Alberti S, Buccione R, Luini A, Mironov AA (2000) Correlative light-electron microscopy reveals the tubular-saccular ultrastructure of carriers operating between Golgi apparatus and plasma membrane. J Cell Biol 148(1):45–58

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Mironov AA, Beznoussenko GV (2009) Correlative microscopy: a potent tool for the study of rare or unique cellular and tissue events. J Microsc 235(3):308–321

    Article  CAS  PubMed  Google Scholar 

  6. Polishchuk RS, Polishchuk EV, Mironov AA (1999) Stack coalescence in MT-deprived cells with fragmented Golgi. Eur J Cell Biol 78:170–185

    Article  CAS  PubMed  Google Scholar 

  7. Mironov AA Jr, Mironov AA (1998) Estimation of subcellular organelle volume from ultrathin sections through centrioles with a discretized version of vertical rotator. J Microsc 192:29–36

    Article  PubMed  Google Scholar 

Download references

Acknowledgment

This work was supported by FIRC, Italy.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Alexander A. Mironov M.D., Ph.D., D.Sc. .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2015 Springer Science+Business Media New York

About this protocol

Cite this protocol

Beznoussenko, G.V., Mironov, A.A. (2015). Correlative Video-Light–Electron Microscopy of Mobile Organelles. In: Tang, B. (eds) Membrane Trafficking. Methods in Molecular Biology, vol 1270. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-2309-0_23

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-2309-0_23

  • Published:

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-2308-3

  • Online ISBN: 978-1-4939-2309-0

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics