Materials and Reagents

1 ml TB syringe with 27-gauge needle (BD Biosciences, catalog number: 309623 )
Plastic wrap
3.5” x 3.5” weigh boat (Thermo Fisher Scientific, Fisher Scientific, catalog number: 8732113 )
1.5-ml microcentrifuge tubes
0.45 µm filter unit (Thermo Fisher Scientific, Fisher Scientific, catalog number: 09-740-65B )
Amicon^TM Ultra-15 centrifugal filter units (Merck Millipore, catalog number: UFC903024 )
5 ml tube
Adult mice (> 6 weeks, any strain) (e.g., Balb/cJ)
⁵⁹FeCl₃ (Perkin Elmer, catalog number: NEZ037500UC )
Note: The minimum specific activity of ⁵⁹Fe we have used to obtain decent signal from our gamma counter was 0.2 Ci/mmol at the concentration of ~3 µCi/µl, which gave whole body counts per minute of ~100,000 per each animal. Our gamma counting efficiency is about 10% for ⁵⁹Fe.
Nitrilotriacetic acid (NTA) (Sigma-Aldrich, catalog number: N9877-100G )
HEPES (Thermo Fisher Scientific, Fisher Scientific, catalog number: AC172570250 )
Tris (Thermo Fisher Scientific, Fisher Scientific, catalog number: BP152-5 )
Sodium bicarbonate (NaHCO₃) (Fisher Scientific, catalog number: S233-500 )
Sodium citrate dihydrate (Thermo Fisher Scientific, Fisher Scientific, catalog number: S279-500 )
Ferric chloride hexahydrate (FeCl₃·6H₂O) (Thermo Fisher Scientific, Fisher Scientific, catalog number: I88-100 )
Hydrochloric acid (HCl) (Thermo Fisher Scientific, Fisher Scientific, catalog number: A144-212 )
Ethanol
Human apo-transferrin (Sigma-Aldrich, catalog number: T2252 )
PBS (VWR, Corning^®, catalog number: 21-040-CM )
Sodium chloride (NaCl) (Thermo Fisher Scientific, Fisher Scientific, catalog number: S2713 )
Fisherbrand^TM absorbent underpads (Thermo Fisher Scientific, Fisher Scientific, catalog number: 14-206-64 )
Radioactive decontaminating solution (Thermo Fisher Scientific, Fisher Scientific, catalog number: NC9633347 )
20 mM Fe-NTA (1:4) (see Recipes)
Ferric citrate solution (see Recipes)
⁵⁹Fe-labeled ferric citrate solution (see Recipes)
⁵⁹Fe-labeled transferrin (see Recipes)
0.9% NaCl solution (see Recipes)

Equipment

Gamma counter (PerkinElmer, catalog number: 2480-0010 )
The program for ⁵⁹Fe detection was set using the following parameters:
1. Counting window: Dynamic-keV
2. Peak position: 1292 keV
3. Low boundary: 1020 keV
4. High boundary: 1400 keV
5. Threshold: 20%
6. Max. assay deviation: 20%
7. Max. normalization deviation: 50%
8. Warning assay deviation: 15%
9. Significant CPM/keV: 10
10. Counting spectrum type: many peaks
Gamma counting tubes (5 x 28 mm) and RIA racks (PerkinElmer, catalog number: 1480-151 )
1. Prior to gamma counting, empty gamma counting tubes are measured to ensure no ⁵⁹Fe contamination (i.e., < 25 CPM = background).
Mouse restrainer (Braintree Scientific, catalog number: MTI STD )
Basic surgical kit for small animals

Procedure

For tissue NTBI uptake measurement, inject 0.1 ml of ferric citrate solution (containing 70 µg iron) to a mouse via tail vein to transiently saturate the iron-binding capacity of plasma transferrin.
This step is required so that any subsequently injected iron will not bind to transferrin and hence will be non-transferrin-bound iron (NTBI). Return the mouse to the cage and wait for 10 min before going to step 2. See Figure 1 for a typical injection station setup.
For tissue TBI uptake measurement, inject 0.1 ml of ⁵⁹Fe-labeled transferrin (containing 150 µg transferrin) to a mouse via tail vein. Return the mouse to the cage and wait for 2 h before going to step 3.

Figure1. Typical setup for tail vein injection station (A) and tissue harvesting station (B)
Inject 0.1 ml of ⁵⁹Fe-labeled ferric citrate solution (2 µCi) to the mouse via tail vein. Return the mouse to the cage.
Two hours after injection of ⁵⁹Fe-labeled ferric citrate solution (for NTBI uptake) or ⁵⁹Fe-labeled transferrin (for TBI uptake), euthanize the mouse with an overdose of isoflurane or other proper methods and place the mouse on an absorbent pad. Cut the mouse tail off to remove residual ⁵⁹Fe radioactivity that is retained in the tail (i.e., radioactivity that did not enter the circulation). See Figure 1 for a typical harvesting station setup.
Sterilize the mouse abdomen and chest area with 70% ethanol. Open the abdominal cavity with blunt-end sterile scissors and collect tissues of interest (e.g., pancreas, spleen, liver, kidney, etc.). Then open the chest cavity to collect tissues such as lung and heart.
Rinse tissue in 0.9% NaCl solution poured in a disposable weigh boat and remove excess liquid by dabbing the tissues on a stack of paper towels.
Use plastic wrap to wrap each tissue briefly prior to transfer into a gamma counting tube to minimize cross contamination of ⁵⁹Fe radioactivity between samples. Optionally, transfer tissue to a clean 1.5-ml microcentrifuge tube if the tissue sample can fit in it. Then measure the tissue radioactivity using a gamma counter by putting the 1.5-ml tube containing the tissue sample into a gamma counting tube rack (see Figure 2).
For the mouse carcass, use plastic wrap to securely wrap the whole carcass prior to transfer into a gamma counting tube (see Figure 2).

Figure 2. Illustration of radioactive tissue handling and loading to gamma counting tubes prior to measurement by a gamma counter. A. Materials required for tissue sample wrapping. B. Top view of the gamma counting rack with previously wrapped samples loaded in each gamma counting tube. C. The gamma counting rack containing the sample tube is placed on the rack belt of the gamma counter, ready to be loaded inside the gamma detector (left panel). The gamma counter screen showing real-time radioactivity being detected from the tissue sample (right panel).
Measure organ and carcass ⁵⁹Fe radioactivity by using a gamma counter. Calculate tissue NTBI and TBI uptakes as a percentage of whole-body counts per minute (CPM) (whole-body CPM = CPM values from all tissues + CPM value from carcass) (see Figure 3).

Figure 3. Example of raw data and analysis of results. Two hours after injection with ⁵⁹Fe-labeled ferric citrate, WT and Zip14 KO mice at 3 weeks of age were sacrificed and their tissues and carcasses were subjected to gamma counting. A. Counts per minute (CPM) values from each sample were recorded. Whole-body CPM values were calculated from the sum of all tissues and carcass CPMs. B. Tissue ⁵⁹Fe accumulation is expressed as % of whole body and calculated as (tissue CPM/whole body CPM) x 100. C. Resultant figure from panel B is shown. Data were analyzed by using unpaired student’s t-test. Values are means ± SE (n = 3/group). ***P < 0.001, **P < 0.01.

Notes

After each experiment, use radioactive cleaning reagent to clean the surgical tools, mouse cages, and related equipment to decontaminate ⁵⁹Fe. Perform a radioactive swipe test on the related equipment and area where the experiment is performed after each experiment to ensure no contamination is observed. Radioactive waste products should be disposed of by following your local Environmental Health and Safety (EH&S) regulations.

Recipes

20 mM Fe-NTA (1:4 molar ratio)
20 mM HEPES/20 mM Tris buffer
0.4 M NTA
0.4 M FeCl₃
1. Prepare 20 mM HEPES/20 mM Tris buffer
  To 450 ml ddH₂O, dissolve 2.38 g HEPES and 1.21 g Tris.
  Adjust pH to 6.0 with 10 N HCl.
  Bring final volume to 500 ml with ddH₂O.
2. Prepare 0.4 M NTA
  In 20 ml 20 mM HEPES/20 mM Tris buffer, add 4.28 g NTA.
  Adjust pH to 6.0 with 10 N NaOH by adding ~3 ml of 10 N NaOH at the beginning then drop-wise until pH reaches 6.0 (Caution: pH changes rapidly between pH 5-7).
  Bring final volume to 56 ml with 20 mM HEPES/20 mM Tris buffer.
3. Prepare 0.4 M FeCl₃ in 100 mM HCl
  To make 100 mM HCl, add 500 µl of 37% (equivalent to 12 M) HCl solution to 11.5 ml ddH₂O.
  Dissolve 1.08 g FeCl₃·6H₂O in 10 ml 100 mM HCl.
4. Prepare 20 mM Fe-NTA (1:4 molar ratio)
  In a 50 ml beaker with stir bar inside, add 10 ml of 20 mM HEPES/20 mM Tris buffer.
  Leave the pH electrode inside the solution and track the solution pH along the rest of the procedure.
  Add 2 ml of 0.4 M FeCl₃ prepared in step 1c. The solution pH should now be ~2.
  Add 8 ml of 0.4 M NTA prepared in step 1b.
  Adjust to final pH of 6.95 with 100 mM NaOH.
  Bring final volume to 40 ml with 20 mM HEPES/20 mM Tris buffer.
  Filter sterilized the 20 mM Fe-NTA solution through 0.45 µm filter unit.
Ferric citrate solution
0.1 M citrate buffer
12.5 mM FeCl₃·6H₂O
1. Prepare 0.1 M citrate buffer
  To 40 ml ddH₂O, dissolve 2.25 g Na₃C₆H₅O₇·2H₂O (tri-sodium citrate dihydrate).
  Adjust pH to 6.6 with 10 M HCl.
  Bring final volume to 50 ml with ddH₂O.
2. For 50 ml stock, add 0.169 g FeCl₃·6H₂O to 50 ml 0.1 M citrate buffer.
⁵⁹Fe-labeled ferric citrate solution
0.1 M citrate buffer, ⁵⁹FeCl₃
To 100 µl 0.1 M citrate buffer, add 2 µCi ⁵⁹FeCl₃.
Mix well.
⁵⁹Fe-labeled transferrin
10 mM NaHCO₃
18.75 µM apo-transferrin
20 mM Fe-NTA (1:4 molar ratio)
⁵⁹FeCl₃
1. To 50 ml PBS, add 0.042 g NaHCO₃.
2. Add 7.5 mg apo-transferrin to 5 ml NaHCO₃ in PBS buffer prepared in step 4a.
3. Add 2.5 µl ⁵⁹FeCl₃ to 12.5 µl of 20 mM Fe-NTA solution.
4. Mix solutions prepared in steps 4b and 4c. Incubate at RT for 1 h to allow ⁵⁹Fe to bind to transferrin.
5. Remove unbound ⁵⁹Fe by using Amicon^TM Ultra-15 centrifugal filter unit.
0.9% NaCl solution, autoclaved
To every 1 L of ddH₂O, add 9 g of NaCl.
Autoclave to sterilize and store at 4 °C until use.

Acknowledgments

This work was supported by the National Institutes of Health grant DK080706 (to M.D.K.). The protocol was adapted from Craven et al. (1987), and a short version of the adapted protocol was published in Jenkitkasemwong et al. (2015).

References

Craven, C. M., Alexander, J., Eldridge, M., Kushner, J. P., Bernstein, S. and Kaplan, J. (1987). Tissue distribution and clearance kinetics of non-transferrin-bound iron in the hypotransferrinemic mouse: a rodent model for hemochromatosis. Proc Natl Acad Sci U S A 84(10): 3457-3461.
Jenkitkasemwong, S., Wang, C. Y., Coffey, R., Zhang, W., Chan, A., Biel, T., Kim, J. S., Hojyo, S., Fukada, T. and Knutson, M. D. (2015). SLC39A14 is required for the development of hepatocellular iron overload in murine models of hereditary hemochromatosis. Cell Metab 22(1): 138-150.