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Macrophage depletion has been used extensively to study autoimmune disease and more recently in tumor models. The clodronate-containing liposomes will be recognized as foreign particles and get engulfed by macrophages upon dosing into the animal by the chosen routes. Consequently, macrophages that have engulfed liposomes will all be destroyed by the liposomal. In the protocol presented here the clodronate-containing liposomes were used to systemically deplete macrophages in mice.

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Protocol for Macrophage Depletion from Mice

Immunology > Animal model > Mouse
Authors: Zuoxiang Xiao
Zuoxiang XiaoAffiliation: Cancer Inflammation Program, NCI-Frederick, NIH, Frederick, USA
For correspondence: xiaoz2@mail.nih.gov
Bio-protocol author page: a1391
 and Qun Jiang
Qun JiangAffiliation: Cancer Inflammation Program, NCI-Frederick, NIH, Frederick, USA
Bio-protocol author page: a1392
Vol 4, Iss 11, 6/5/2014, 4224 views, 0 Q&A, How to cite
DOI: http://dx.doi.org/10.21769/BioProtoc.1144

[Abstract] Macrophage depletion has been used extensively to study autoimmune disease and more recently in tumor models. The clodronate-containing liposomes will be recognized as foreign particles and get engulfed by macrophages upon dosing into the animal by the chosen routes. Consequently, macrophages that have engulfed liposomes will all be destroyed by the liposomal. In the protocol presented here the clodronate-containing liposomes were used to systemically deplete macrophages in mice.

Materials and Reagents

  1. Mice
  2. Clodronate (dichloromethylene diphosphonic acid)-loaded liposomes (VUmc)
  3. PBS-containing liposomes (VUmc)
  4. Phosphatidyl choline (Lipoid GmbH, catalog number: D-67065)
  5. Cholesterol (Sigma-Aldrich, catalog number: C8667)
  6. Liposomes (see Recipes)
  7. Liposomes suspended in sterile phosphate buffered saline (see Recipes)

Equipment

  1. Syringe (10 ml and 1 ml) (BD, catalog numbers: 309604 and 305111)
  2. 26 G 1/2 needles (BD, catalog number: 309659)

Procedure

  1. Twenty, 8-week-old mice were randomly divided into two groups.
  2. One group of mice were intravenously injected t using 1-ml syringe with 26 G 1/2 needles, twice per week with clodronate-loaded liposomes in 150 µl for the first month and 100 µl following the first month’s injection to reduce possible side effects, such as infection, live toxicity et al. The mice were treated for 3 months totally.
  3. The second group was treated with PBS-liposomes.
  4. At different time points (such as 2, 4, 8 weeks after treatments) of the experiment, one or two mice from each group will be euthanized to examine inflammation and other interesting analysis. Based on our experiments, the FACS analysis detected around 90% of macrophage reduction in the group that treated with the clodronate-loaded liposomes versus the control group after 2 weeks treatment, and this reduction kept to the end of the experiments.
  5. During the whole treatment period, the treated mice need to be closely monitored for the possible signs and symptoms such as weight loss, yellow, bloody, or tar-colored stool, dark urine color, diarrhea, fatigue etc.
  6. At the end of the experiment, (depend on the experiment), the mice were euthanized and the lung tissues were collected for various analyses.

Recipes

Notes:

  1. Based on the instructions from company.
  2. The clodronate-loaded liposomes and PBS-containing liposomes are ready for use, but the solutions that usually kept in 4 °C need to be warmed up to room temperature before injections.
  1. Liposomes
    Liposomes are artificial lipid spherules made of:
    1. Phosphatidyl choline
    2. Cholesterol
  2. Phosphate buffered saline (PBS)
    1. 10 mM Na2HPO4
    2. 10 mM NaH2PO4
    3. 140 mM NaCI

Acknowledgments

We thank Yinling Hu, Robert H. Wiltrout and Jami Willette-Brown from Frederick National Laboratory for Cancer Research for their support and suggestions on the experimental design. This work was supported by the National Cancer Institute (ZIA BC 011212 and ZIA BC 011391 to Y.H.).

References

  1. Xiao, Z., Jiang, Q., Willette-Brown, J., Xi, S., Zhu, F., Burkett, S., Back, T., Song, N. Y., Datla, M., Sun, Z., Goldszmid, R., Lin, F., Cohoon, T., Pike, K., Wu, X., Schrump, D. S., Wong, K. K., Young, H. A., Trinchieri, G., Wiltrout, R. H. and Hu, Y. (2013). The pivotal role of IKKalpha in the development of spontaneous lung squamous cell carcinomas. Cancer Cell 23(4): 527-540.


How to cite this protocol: Xiao, Z. and Jiang, Q. (2014). Protocol for Macrophage Depletion from Mice . Bio-protocol 4(11): e1144. DOI: 10.21769/BioProtoc.1144; Full Text



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