Skip to main content

Visualization and Quantitative Analysis of the Actin Cytoskeleton Upon B Cell Activation

  • Protocol
  • First Online:
B Cell Receptor Signaling

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1707))

Abstract

The formation of the immunological synapse upon B cell activation critically depends on the rearrangement of the submembranous actin cytoskeleton. Polymerization of actin monomers into filaments provides the force required for B cell spreading on the antigen-presenting cell (APC). Interestingly, the actin network also participates in cellular signaling at multiple levels. Fluorescence microscopy plays a critical role in furthering our understanding of the various functions of the cytoskeleton, and has become an important tool in the studies on B cell activation. The actin cytoskeleton can be tracked in live cells with various fluorescent probes binding to actin, or in fixed cells typically with phalloidin staining. Here, we present the usage of TIRF microscopy and an image analysis workflow for studying the overall density and organization of the actin network upon B cell spreading on antigen-coated glass, a widely used model system for the formation of the immunological synapse.

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

Access this chapter

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

Institutional subscriptions

References

  1. Le Floc’h A, Huse M (2015) Molecular mechanisms and functional implications of polarized actin remodeling at the T cell immunological synapse. Cell Mol Life Sci 72:537–556. https://doi.org/10.1007/s00018-014-1760-7

    Article  PubMed  Google Scholar 

  2. Batista FD, Iber D, Neuberger MS (2001) B cells acquire antigen from target cells after synapse formation. Nature 411:489–494. https://doi.org/10.1038/35078099

    Article  CAS  PubMed  Google Scholar 

  3. Kuokkanen E, Šuštar V, Mattila PK (2015) Molecular control of B cell activation and immunological synapse formation. Traffic 16:311–326. https://doi.org/10.1111/tra.12257

    Article  CAS  PubMed  Google Scholar 

  4. Mattila PK, Batista FD, Treanor B (2016) Dynamics of the actin cytoskeleton mediates receptor cross talk: an emerging concept in tuning receptor signaling. J Cell Biol 212:267–280. https://doi.org/10.1083/jcb.201504137

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Gasparrini F, Feest C, Bruckbauer A, Mattila PK, Müller J, Nitschke L, Bray D, Batista FD (2015) Nanoscale organization and dynamics of the siglec CD22 cooperate with the cytoskeleton in restraining BCR signalling. EMBO J 35:1–23. 10.15252/embj.201593027

    Google Scholar 

  6. Mattila PK, Feest C, Depoil D, Treanor B, Montaner B, Otipoby KL, Carter R, Justement LB, Bruckbauer A, Batista FD (2013) The actin and tetraspanin networks organize receptor nanoclusters to regulate B cell receptor-mediated signaling. Immunity 38:461–474. https://doi.org/10.1016/j.immuni.2012.11.019

    Article  CAS  PubMed  Google Scholar 

  7. Treanor B, Depoil D, Bruckbauer A, Batista FD (2011) Dynamic cortical actin remodeling by ERM proteins controls BCR microcluster organization and integrity. J Exp Med 208:1055–1068. https://doi.org/10.1084/jem.20101125

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Derry JM, Ochs HD, Francke U (1994) Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 78:635–644. doi: 0092-8674(94)90528-2 [pii]

    Article  CAS  PubMed  Google Scholar 

  9. Machesky LM, Insall RH (1998) Scar1 and the related Wiskott–Aldrich syndrome protein, WASP, regulate the actin cytoskeleton through the Arp2/3 complex. Curr Biol 8:1347–1356. https://doi.org/10.1016/S0960-9822(98)00015-3

    Article  CAS  PubMed  Google Scholar 

  10. Freeman S, Lei V, Dang-Lawson M, Mizuno K, Roskelley CD, Gold MR (2011) Cofilin-mediated F-actin severing is regulated by the rap GTPase and controls the cytoskeletal dynamics that drive lymphocyte spreading and BCR microcluster formation. J Immunol 187:5887–5900. https://doi.org/10.4049/jimmunol.1102233

    Article  CAS  PubMed  Google Scholar 

  11. Wulf E, Deboben a BF a, Faulstich H, Wieland T (1979) Fluorescent phallotoxin, a tool for the visualization of cellular actin. Proc Natl Acad Sci U S A 76:4498–4502. https://doi.org/10.1073/pnas.76.9.4498

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  12. Ballestrem C, Wehrle-Haller B, B a I (1998) Actin dynamics in living mammalian cells. J Cell Sci 111(Pt 1):1649–1658

    CAS  PubMed  Google Scholar 

  13. Melak M, Plessner M, Grosse R (2017) Actin visualization at a glance. J Cell Sci 130(3):525–530. https://doi.org/10.1242/jcs.189068

    Article  PubMed  Google Scholar 

  14. Belin BJ, Goins LM, Mullins RD (2014) Comparative analysis of tools for live cell imaging of actin network architecture. BioArchitecture 4:189–202. https://doi.org/10.1080/19490992.2014.1047714

    Article  PubMed  Google Scholar 

  15. Riedl J, Crevenna AH, Kessenbrock K, Yu JH, Neukirchen D, Bista M, Bradke F, Jenne D, T a H, Werb Z, Sixt M, Wedlich-Soldner R (2008) Lifeact: a versatile marker to visualize F-actin. Nat Methods 5:605–607. https://doi.org/10.1038/nmeth.1220

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Balagopalan L, Sherman E, V a B, Samelson LE (2011) Imaging techniques for assaying lymphocyte activation in action. Nat Rev Immunol 11:21–33. https://doi.org/10.1038/nri2903

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Axelrod D (1981) Cell-substrate contacts illuminated by total-internal reflection fluorescence. J Cell Biol 89:141–145. https://doi.org/10.1083/jcb.89.1.141

    Article  CAS  PubMed  Google Scholar 

  18. Mattheyses AL, Shaw K, Axelrod D (2006) Effective elimination of laser interference fringing in fluorescence microscopy by spinning azimuthal incidence angle. Microsc Res Tech 69:642–647. https://doi.org/10.1002/jemt.20334

    Article  PubMed  Google Scholar 

  19. Williams GT, Peaker CJG, Patel KJ, Neuberger MS (1994) The α/β sheath and its cytoplasmic tyrosines are required for signaling by the B-cell antigen receptor but not for capping or for serine/threonine-kinase recruitment. Proc Natl Acad Sci U S A 91:474–478. https://doi.org/10.1073/pnas.91.2.474

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  20. Jankowska KI, Burkhardt JK (2017) The immune. Synapse 1584:7–29. https://doi.org/10.1007/978-1-4939-6881-7

    Google Scholar 

  21. Chicaybam L, Sodre AL, Curzio BA, Bonamino MH (2013) An efficient low cost method for gene transfer to T lymphocytes. PLoS One 8(3):e60298. https://doi.org/10.1371/journal.pone.0060298

    Article  CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgments

Imaging was performed at the Cell Imaging Core, Turku Centre for Biotechnology, University of Turku and Åbo Akademi University. We thank Markku Saari and Jouko Sandholm from the Cell Imaging Core for their help with the microscopes, and the whole Mattila lab for their critical comments to the manuscript. Turku University Hospital (TYKS) is acknowledged for the support in basic laboratory materials. This work was supported by the Academy of Finland (grant ID: 25700, 296684 and 307313 for PKM, and 286712 for VŠ), University of Turku Graduate School (UTUGS) (for MV), VSSHP research support (for PKM), as well as Sigrid Juselius (for PKM), Jane and Aatos Erkko (for PKM), Magnus Ehrnrooth (for PKM and VŠ) and Finnish Cultural (for VŠ) foundations.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pieta K. Mattila .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2018 Springer Science+Business Media, LLC

About this protocol

Check for updates. Verify currency and authenticity via CrossMark

Cite this protocol

Šuštar, V., Vainio, M., Mattila, P.K. (2018). Visualization and Quantitative Analysis of the Actin Cytoskeleton Upon B Cell Activation. In: Liu, C. (eds) B Cell Receptor Signaling. Methods in Molecular Biology, vol 1707. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-7474-0_18

Download citation

  • DOI: https://doi.org/10.1007/978-1-4939-7474-0_18

  • Published:

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-7473-3

  • Online ISBN: 978-1-4939-7474-0

  • eBook Packages: Springer Protocols

Publish with us

Policies and ethics