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Immunostaining of Macrophages, Endothelial Cells, and Smooth Muscle Cells in the Atherosclerotic Mouse Aorta

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Methods in Mouse Atherosclerosis

Part of the book series: Methods in Molecular Biology ((MIMB,volume 1339))

Abstract

The atherosclerotic mouse aorta consists of a heterogeneous population of cells, including macrophages, endothelial cells, and smooth muscle cells that play critical roles in cardiovascular disease. Identification of these vascular cells in the vessel wall is important to understanding their function in pathological conditions. Immunohistochemistry is an invaluable technique used to detect the presence of cells in different tissues. Here, we describe immunohistochemical techniques commonly used for the detection of the vascular cells in the atherosclerotic mouse aorta using cell type-specific markers.

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References

  1. Reddick RL, Zhang SH, Maeda N (1994) Atherosclerosis in mice lacking apo E. Evaluation of lesional development and progression. Arterioscler Thromb 14:141–147

    Article  CAS  PubMed  Google Scholar 

  2. Rong JX, Li J, Reis ED et al (2001) Elevating high-density lipoprotein cholesterol in apolipoprotein E-deficient mice remodels advanced atherosclerotic lesions by decreasing macrophage and increasing smooth muscle cell content. Circulation 104:2447–2452

    Article  CAS  PubMed  Google Scholar 

  3. Ramos-Vara JA (2011) Principles and methods of immunohistochemistry. Methods Mol Biol 691:83–96

    Article  CAS  PubMed  Google Scholar 

  4. Trogan E, Choudhury RP, Dansky HM et al (2002) Laser capture microdissection analysis of gene expression in macrophages from atherosclerotic lesions of apolipoprotein E-deficient mice. Proc Natl Acad Sci 99:2234–2239

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  5. Gage GJ, Kipke DR, Shain W (2012) Whole animal perfusion fixation for rodents. J Vis Exp 65:3564

    PubMed  Google Scholar 

  6. Gautier EL, Shay T, Miller J et al (2012) Gene-expression profiles and transcriptional regulatory pathways that underlie the identity and diversity of mouse tissue macrophages. Nat Immunol 13:1118–1128

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  7. Gimbrone MA Jr (1995) Vascular endothelium: an integrator of pathophysiologic stimuli in atherosclerosis. Am J Cardiol 75:67B–70B

    Article  CAS  PubMed  Google Scholar 

  8. Muller AM, Hermanns MI, Skrzynski C et al (2002) Expression of the endothelial markers PECAM-1, vWf, and CD34 in vivo and in vitro. Exp Mol Pathol 72:221–229

    Article  PubMed  Google Scholar 

  9. Skalli O, Ropraz P, Trzeciak A et al (1986) A monoclonal antibody against alpha-smooth muscle actin: a new probe for smooth muscle differentiation. J Cell Biol 103:2787–2796

    Article  CAS  PubMed  Google Scholar 

  10. Yoshida T, Owens GK (2005) Molecular determinants of vascular smooth muscle cell diversity. Circ Res 96:280–291

    Article  CAS  PubMed  Google Scholar 

  11. Feig JE, Rong JX, Shamir R et al (2011) HDL promotes rapid atherosclerosis regression in mice and alters inflammatory properties of plaque monocyte-derived cells. Proc Natl Acad Sci U S A 108:7166–7171

    Article  PubMed Central  CAS  PubMed  Google Scholar 

  12. Breslow JL (1996) Mouse models of atherosclerosis. Science 272:685–688

    Article  CAS  PubMed  Google Scholar 

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Acknowledgments

This work is supported by NIH HL 084312 and HL098055 to E.A.F, and NIH T32 grant 5T32HL098129-05 to P.M.

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Correspondence to Edward A. Fisher M.D., Ph.D. .

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Menon, P., Fisher, E.A. (2015). Immunostaining of Macrophages, Endothelial Cells, and Smooth Muscle Cells in the Atherosclerotic Mouse Aorta. In: Andrés, V., Dorado, B. (eds) Methods in Mouse Atherosclerosis. Methods in Molecular Biology, vol 1339. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-2929-0_9

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  • DOI: https://doi.org/10.1007/978-1-4939-2929-0_9

  • Publisher Name: Humana Press, New York, NY

  • Print ISBN: 978-1-4939-2928-3

  • Online ISBN: 978-1-4939-2929-0

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