Register for email alerts and news feeds:
This journal | BMJ Group
rss
Heart 1998;80:509-516; doi:10.1136/hrt.80.5.509
Copyright © 1998 BMJ Publishing Group Ltd & British Cardiovascular Society

Heart 1998;80:509-516 ( November )

Intravascular stents: a new technique for tissue processing for histology, immunohistochemistry, and transmission electron microscopy

N Malik, J Gunn, C M Holt, L Shepherd, S E Francis, C M H Newman, D C Crossman, D C Cumberland

Cardiovascular Medicine, University of Sheffield, Clinical Sciences Centre, Northern General Hospital, Herries Road, Sheffield S5 7AU, UK

Correspondence to: Dr Malik.

Accepted for publication 22 May 1998

Background---Study of the vascular response to stent implantation has been hampered by difficulties in sectioning metal and tissue without distortion of the tissue stent interface. The metal is often removed before histochemical processing, causing a loss of arterial architecture. Histological and immunohistochemical sections should be 5 µm with an intact tissue stent interface.
Objectives---To identify the most suitable cutting and grinding equipment, embedding resin, and slides for producing thin sections of stented arteries with the stent wires in situ for histological, immunohistochemical, and transmission electron microscopic (TEM) analyses.
Methods---20 balloon stainless steel stents were implanted in the coronary arteries of 10 pigs. Twenty eight days later the stented arterial segments were excised, formalin fixed, embedded in five different resins (Epon 812, LR white, T9100, T8100, and JB4), and sectioned with two different high speed saws and a grinder for histological, immunohistochemical, and TEM analyses. Five stented human arteries were obtained at necropsy and processed using the best of the reported methods.
Results---The Isomet precision saw and grinder/polisher unit reliably produced 5 µm sections with most embedding resins; minimum section thickness with the horizontal saw was 400 µm. Resin T8100, a glycol methacrylate, enabled satisfactory sectioning, grinding, and histological (toluidine blue, haematoxylin and eosin, and trichromatic and polychromatic stains) and immunohistochemical analyses (alpha  smooth muscle actin, von Willebrand factor, vimentin, proliferating cell nuclear antigen, and CD68 (mac 387)). T9100 and T8100 embedded stented sections were suitable for ultrastructural examination with TEM. Stented human arterial sections showed preserved arterial architecture with the struts in situ.
Conclusion---This study identified the optimal methods for embedding, sawing, grinding, and slide mounting of stented arteries to achieve 5 µm sections with an intact tissue metal interface, excellent surface qualities, histological and immunohistochemical staining properties, and suitability for TEM examination. The technique is applicable to experimental and clinical specimens.

Keywords: stents;  resin;  histology;  immunohistochemistry;  transmission electron microscopy


© 1998 by Heart

Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

This article has been cited by other articles:

  • Foth, R., Quentin, T., Michel-Behnke, I., Vogt, M., Kriebel, T., Kreischer, A., Ruschewski, W., Paul, T., Sigler, M. (2009). Immunohistochemical Characterization of Neotissues and Tissue Reactions to Septal Defect-Occlusion Devices. Circ Cardiovasc Interv 2: 90-96 [Abstract] [Full Text]  
  • Evans, D.J.W, Lawford, P.V, Gunn, J, Walker, D, Hose, D.R, Smallwood, R.H, Chopard, B, Krafczyk, M, Bernsdorf, J, Hoekstra, A (2008). The application of multiscale modelling to the process of development and prevention of stenosis in a stented coronary artery. Phil Trans R Soc A 366: 3343-3360 [Abstract] [Full Text]  
  • Rousselle, S., Wicks, J. (2008). Preparation of Medical Devices for Evaluation. Toxicol Pathol 36: 81-84 [Abstract] [Full Text]  
  • Sigler, M., Jux, C. (2007). Biocompatibility of septal defect closure devices. Heart 93: 444-449 [Abstract] [Full Text]  
  • Rippstein, P., Black, M. K., Boivin, M., Veinot, J. P., Ma, X., Chen, Y.-X., Human, P., Zilla, P., O'Brien, E. R. (2006). Comparison of Processing and Sectioning Methodologies for Arteries Containing Metallic Stents. J. Histochem. Cytochem. 54: 673-681 [Abstract] [Full Text]  
  • Morton, A. C., Arnold, N. D., Gunn, J., Varcoe, R., Francis, S. E., Dower, S. K., Crossman, D. C. (2005). Interleukin-1 receptor antagonist alters the response to vessel wall injury in a porcine coronary artery model. Cardiovasc Res 68: 493-501 [Abstract] [Full Text]  
  • Johnson, T. W., Wu, Y. X., Herdeg, C., Baumbach, A., Newby, A. C., Karsch, K. R., Oberhoff, M. (2005). Stent-Based Delivery of Tissue Inhibitor of Metalloproteinase-3 Adenovirus Inhibits Neointimal Formation in Porcine Coronary Arteries. Arterioscler. Thromb. Vasc. Bio. 25: 754-759 [Abstract] [Full Text]  
  • Morton, A C, Arnold, N D, Crossman, D C, Gunn, J (2004). Response of very small (2 mm) porcine coronary arteries to balloon angioplasty and stent implantation. Heart 90: 324-327 [Abstract] [Full Text]  
  • Gunn, J, Arnold, N, Chan, K H, Shepherd, L, Cumberland, D C, Crossman, D C (2002). Coronary artery stretch versus deep injury in the development of in-stent neointima. Heart 88: 401-405 [Abstract] [Full Text]  
  • Alp, N. J, West, N. E.J, Arnold, N., Gunn, J., Banning, A. P, Channon, K. M (2002). Increased intimal hyperplasia in experimental vein graft stenting compared to arterial stenting: comparisons in a new rabbit model of stent injury. Cardiovasc Res 56: 164-172 [Abstract] [Full Text]  
  • Brasen, J. H., Kivela, A., Roser, K., Rissanen, T. T., Niemi, M., Luft, F. C., Donath, K., Yla-Herttuala, S. (2001). Angiogenesis, Vascular Endothelial Growth Factor and Platelet-Derived Growth Factor-BB Expression, Iron Deposition, and Oxidation-Specific Epitopes in Stented Human Coronary Arteries. Arterioscler. Thromb. Vasc. Bio. 21: 1720-1726 [Abstract] [Full Text]  

This Article

Services
Citing Articles
Google Scholar
PubMed
Topic Collections
Bookmark with

Register for free content

The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.