Cookies on PerkinElmer
PerkinElmer uses cookies to ensure that we give you the best experience possible on our website. This may include cookies from third party websites. If you continue without changing your settings, we will assume that you consent to receive cookies from this website. You can change your cookie settings at any time. To learn more, please review our cookie policy, which includes information on how to manage your cookies.

Chromium-51 Release Assay

Overview


Chromium-51 (51Cr) release assays are commonly used for the precise and accurate quantification of cytotoxicity, particularly in the study of tumor and viral cytolysis. The assay is used to determine the number of lymphocytes produced in response to infection or drug treatment.

A brief overview of the assay principle is illustrated below. Target cells are labeled with 51Cr, the label is then released from the target cells by cytolysis. The label can be isolated by centrifuging the samples and collecting the supernatants. Supernatants from centrifugation can either be counted directly in a gamma counter, or mixed with scintillation cocktail in a microplate (or dried on a LumaPlate™) and counted in a liquid scintillation counter.

Principle of the chromium release assay
Figure 1. Principle of the chromium release assay. The procedure can be divided into 3 main steps: 51Cr labeling the target cell, release of the 51Cr label by cytolysis, and detection of the released 51Cr label.

Top


What do I need to run this assay?


Required to run the general assay:

  • Chromium-51 (see next section for PerkinElmer product numbers)
  • Cell Culture Media
  • Buffer, such as PBS (optional)
  • Detergent, such as Triton-X or SDS, to obtain maximum release values
  • Tubes or microplates (96 well round-bottom) for cell incubations, depending on assay format
  • Centrifuge for tubes or microplates, depending on assay format

 

Required for detection of Chromium-51:

Gamma Counting (e.g. WIZARD®Gamma Counter):

  • Polystyrene vials

Liquid Scintillation Counting (e.g. Tri-Carb® vial-based counter):

  • Polyethylene or glass vials
  • Scintillation Cocktail -- Ultima Gold™ (6013321)

Liquid Scintillation Counting (e.g. TopCount® or MicroBeta® plate-based counters):

  • For top reading instruments (Microbeta2®, TopCount®) -- PicoPlate™ (6005162) or OptiPlate™ (6005299)
  • For bottom reading instruments (MicroBeta®) -- Flexible plate (1450-401) or IsoPlate (6005040)
  • Scintillation Cocktail -- OptiPhase Supermix (1200-439), MicroScint™-20 (6013261), or MicroScint™ -40 (6013641)
  • Optional: LumaPlates™ (6006633) can be used in top reading instruments in place of plates mentioned above.  Samples are dried in LumaPlates™ overnight and counted without the addition of scintillation cocktail.
  • TopSeal-A™ (6050185)
  • Optional: Plate Shaker

Top


Product and catalog numbers


CompoundSpecific ActivityRad. conc.Packaging bufferStorage temp.Half LifeFresh Lot DateCat. Number

Sodium Chromate

400-1200 Ci/g5 mCi/mLSaline, pH 8-10, sterileRoom Temperature27.7 daysEvery other FridayNEZ030

Sodium Chromate

400-1200 Ci/g1 mCi/mLSaline, pH 8-10, sterileRoom Temperature27.7 daysEvery other FridayNEZ030S

Top


Protocol-in-brief


chromium_workflow_ASK.jpg
Figure 2. Protocol for chromium release assay. Either Gamma or Beta Counting can be used for Cr51 detection.

Important Controls

Spontaneous Release: Target cells without Effector cells.  Incubate Target cells with an equal volume of media or buffer only.

Maximum Release: Incubate Target cells with media or buffer containing 1-2% detergent to completely lyse Target cells (e.g. SDS, Triton X-100).

Percent Specific Lysis: [( Experimental Release – Spontaneous Release)/ (Maximum Release – Spontaneous Release)] * 100.

Assay Optimization

Experimental conditions such as the amount of radioactivity used to label target cells, the length of the target cell labeling incubation, E:T ratios, and E:T incubation times will vary based on cell types used and should be optimized for your particular assay.  

Gamma vs. Beta Counting Efficiency

Traditionally, 51Cr is considered a gamma emitter. However, since 51Cr decays by electron capture it can be quantified by detection of the gamma ray in a gamma counter or by the detection of the more abundant Auger electrons and low energy x-rays in a liquid scintillation counting system. This is reflected in the counting efficiency in each method. In a gamma counter, counting efficiency is unlikely to be in excess of 7%. In an instrument such as the MicroBeta®, 51Cr counting efficiency is 26%.

Top


Sample protocol and data


Sample Protocol

  1. Infect P815 Target cells (2 x 106) with recombinant vaccinia virus (107 pfu) that express the nucleoprotein gene.
  2. Resuspend Target cells for labeling in 50 µl of IMDM (7.5% FCS) plus 50 µCi of Na251CrO4 for one hour.
  3. Wash cells and resuspend in IMDM.
  4. Add 104 Target cells/well of a round-bottom 96 well plate.
  5. Add Effector cells (CTL taken from BALB/cByJ mice immunized with the recombinant vaccinia virus) at E:T ratios of 27:1, 9:1, 3:1, and 1:1. Incubate 4 hours at 37°C.
  6. Prepare important controls (Spontaneous Release, Maximum Release) and incubate 4 hours at 37°C.
  7. Centrifuge samples and collect supernatant.
  8. Add 30 µl supernatant to a polystyrene tube (for gamma counting) and count on Wizard®.
  9. OR for liquid scintillation counting, add 30 µl of supernatant to either a PicoPlate™ well plus 250 µl MicroScint™-20 (shake plate to mix), or a LumaPlate™ well and then air dry. Seal plate and count on TopCount®.

Sample Data

Obtained from following the above Sample Protocol

chromium_lysis_ASK.jpg
Figure 3. Comparison of the percent specific lysis between supernatants counted in tubes on a gamma counter and counted on a TopCount® in LumaPlates™ or PicoPlates™. Killing measured via gamma counting had a range of 9.5% to 68.2%, while TopCount® produced similar ranges using PicoPlates™, 11.7% to 63.9%, and LumaPlates™, 12.3% to 73.5%.

Top


Citations


1. Mickel, R.A., Kessler, D.J., Taylor, J.M, and Licktenstein, A.  Natural Killer Cell Cytotoxicity in the Peripheral Blood, Cervical Lymph Nodes, and Tumor of Head and Neck Cancer Patients.  Cancer Res 48, 5017-5022 (1988). Link

2. Olson, L.M. & Visek, W.J.  Kinetics of Cell-Mediated Cytotoxicity in Mice Fed Diets of Various Fat Contents. J. Nutr 120, 619-624 (1990). Link

3. Lavie, G., Meruelo, D., Aroyo, K., and Mandel, M.  Inhibition of the CD8+ T cell-mediated cytotoxicity reaction by hypericin: potential for treatment of T cell-mediated diseases.  Int. Immunol 12, 479-486 (2000). Link

4. Lamikanra, A., Pan, Z., Isaacs, S.N., Wu, T., & Paterson, Y.  Regression of Established Human Papillomavirus Type 16 (HPV-16) Immortalized Tumors In Vivo by Vaccinia Viruses Expressing Different Forms of HPV-16 E& Correlates with Enhanced     CD8+ T-Cell Responses That Home to the Tumor Site. J. Virol 75, 9654-9664 (2001). Link

5. Schmidt, K.N., Leung, B., Kwong, M., Zarember, K.A., Satyal, S., Navas, T.A., Wang, F., and Godowski, P.J.  APC-Independent Activation of NK Cells by the Toll-Like Receptor 3 Agonist Double-Stranded RNA.  J. Immunol 172, 138-143 (2004). Link

6. Wallace, D., Hildesheim, A. & Pinto, L.A.  Comparison of Benchtop Microplate Beta Counters with the Traditional Gamma Counting Method for Measurement of Chromium-51 Release in Cytotoxic Assays. Clin Vaccine Immunol 11, 255-260 (2004). Link

Top


Other PerkinElmer assays for cytotoxicity


DELFIA® TRF cell cytotoxicity assay 

Top


Custom conjugation and custom assay development at PerkinElmer


PerkinElmer offers custom radiolabeling services.  If you are interested in custom assay development, please contact our custom teams:

ON>POINT® Custom Labeling and Conjugation Services

Top