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This protocol is optimized for immunoFISH staining of OCT section of mouse tissues. It combines immunofluorescence for DNA damage response factors (e.g. 53BP1) (Le et al., 2010) and FISH against telomeric DNA.

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ImmunoFISH for Mice and Baboons Frozen Sections

Cell Biology > Cell imaging > Fluorescence
Authors: Francesca Rossiello
Francesca RossielloAffiliation: The FIRC Institute for Molecular Oncology, IFOM, Milan, Italy
Bio-protocol author page: a1070
Marzia Fumagalli
Marzia FumagalliAffiliation: The FIRC Institute for Molecular Oncology, IFOM, Milan, Italy
Bio-protocol author page: a1071
 and Fabrizio d’Adda di Fagagna
Fabrizio d’Adda di FagagnaAffiliation: The FIRC Institute for Molecular Oncology, IFOM, Milan, Italy
For correspondence: fabrizio.dadda@ifom.eu
Bio-protocol author page: a1072
Vol 3, Iss 24, 12/20/2013, 2117 views, 0 Q&A, How to cite
DOI: http://dx.doi.org/10.21769/BioProtoc.1000

[Abstract] This protocol is optimized for immunoFISH staining of OCT section of mouse tissues. It combines immunofluorescence for DNA damage response factors (e.g. 53BP1) (Le et al., 2010) and FISH against telomeric DNA.

Keywords: ImmunoFISH, DNA damage response, Telomeres, Baboon tissues

Materials and Reagents

  1. Tissue
  2. OCT
  3. 4% formaldehyde
  4. PBS
  5. Triton
  6. Goat serum
  7. BSA
  8. Primary antibody: 53BP1 #NB 100-304 rabbit from Novus
  9. Second antibody: goat anti-rabbit Alexa Fluor® 488 Dye
  10. Triton
  11. Glycine
  12. Mowiol 4-88 reagent (Calbiochem®)
  13. Formamide
  14. Tris HCl, pH 7.4
  15. Telomeric PNA probe (TelC-Cy3 from PANAGENE, catalog number: F1002-5)
  16. Tween-20
  17. DAPI
  18. Hybridization mixture (see Recipes)
  19. Blocking reagent (Roche Diagnostics, catalog number: 11096176001) (see Recipes)
  20. Wash solution I (see Recipes)
  21. Wash solution II (see Recipes)

Equipment

  1. Glass slide
  2. Metal thermoblock
  3. Humidified chamber

Procedure

  1. Frozen tissue placed in OCT without fixation.
  2. When needed, slice to the desired thickness (8-10 micron), dry the slides few minutes (often the time to prepare the other slides) and freeze again at -80 °C.
  3. The day of the staining, thaw the slides and fix for 20 min in 4% formaldehyde.
  4. Wash slides with PBS for 3 x 5 min at RT.
  5. Permeabilize slides with 0.5% Triton in PBS for 5 min at RT.
  6. Wash 2x with PBS 5 min at RT.
  7. Block in 5% Goat serum diluted in PBS + 1% BSA for 60 min.
  8. Incubate at 4 °C: 53BP1 #NB 100-304 (rabbit from Novus) 1:100 in PBS, 2.5% goat serum, 1% BSA. Use 60-80 μl for each slide.
  9. Wash once quickly and 3 x 10 min with PBS at RT.
  10. Secondary: goat anti-rabbit (Alexa 488) (1/100) in PBS + 1% BSA for 60 min at RT.
  11. Wash once quickly and 3 x 10 min with PBS RT.
  12. Re-fix tissue with PFA 4% + Triton 0.1%, 10 min RT.
  13. Incubate with glycine 10 mM in H2O, 30 min, RT.
  14. Wash with 1x PBS, 3 times, 5 min.
  15. Prepare the hybridization mixture and put 30-50 μl directly on the sample.
  16. Put a glass slide carefully on the drop without making bubbles.
  17. Put the slide directly on a metal thermoblock at 80 °C, 5 min.
  18. Hybridize in a humidified chamber, 2 h, RT.
  19. Remove glass from the slide.
  20. Wash with Wash solution I, twice, 15 min.
  21. Wash with Wash solution II, 3 times, 5 min.
  22. Incubate with DAPI, 2 min, RT.
  23. Wash briefly with 1x PBS.
  24. Mount with mowiol.
  25. Store the slides at 4 °C for short time storage (2 weeks) or at -20 °C. It is recommended to analyze the fluorescence as soon as possible to avoid fluorophore fading.


    Figure 1. A representative figure of ImmunoFISH stained mouse hippocampus tissue. DAPI is in blue, 53BP1is in green and telomeric PNA probe is in red.

Recipes

  1. Hybridization mixture (always prepare fresh)
    Formamide
    70%
    Blocking reagent
    1x
    Tris HCl pH 7.4
    10 mM
    Telomeric PNA probe
    0.5 μM
    H2O
    to volume
  2. 10x Blocking reagent
    Prepare small aliquots and store them at -20 °C.
  3. Wash Solution I (250 ml) (always prepare fresh)
    Formamide
    175 ml
    BSA 10%
    2.5 ml
    Tris HCl 1 M pH 7.4
    2.5 ml
    H2O
    to volume
  4. Wash Solution II (350 ml) (always prepare fresh)
    Tris HCl 1 M pH 7.4
    35 ml
    NaCl 5 M
    10.5 ml
    Tween-20 10%
    2.5 ml
    H2O
    to volume

Acknowledgments

The immunofluorescence part of the protocol is adapted from Le et al. (2010). The F.d’A.d.F. laboratory is supported by FIRC (Fondazione Italiana per la Ricerca sul Cancro), AIRC (Associazione Italiana per la Ricerca sul Cancro), European Union (GENINCA, contract number 202230), HFSP (Human Frontier Science Program), AICR (Association for International Cancer Research), EMBO Young Investigator Program and Telethon.

References

  1. Fumagalli, M., Rossiello, F., Clerici, M., Barozzi, S., Cittaro, D., Kaplunov, J. M., Bucci, G., Dobreva, M., Matti, V. and Beausejour, C. M. (2012). Telomeric DNA damage is irreparable and causes persistent DNA-damage-response activation. Nat Cell Biol 14(4): 355-365.
  2. Le, O. N., Rodier, F., Fontaine, F., Coppe, J. P., Campisi, J., DeGregori, J., Laverdière, C., Kokta, V., Haddad, E. and Beauséjour, C. M. (2010). Ionizing radiation‐induced long‐term expression of senescence markers in mice is independent of p53 and immune status. Aging Cell 9(3): 398-409.


How to cite this protocol: Rossiello, F., Fumagalli, M. and di Fagagna, F. d. (2013). ImmunoFISH for Mice and Baboons Frozen Sections. Bio-protocol 3(24): e1000. DOI: 10.21769/BioProtoc.1000; Full Text



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