Histopathological analysis of cellular localization of cathepsins in abdominal aortic aneurysm wall

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Fabian Lohoefer - , Technical University of Munich (Author)
  • Christian Reeps - , Department of Visceral, Thoracic and Vascular Surgery, Hospital of the Ludwig-Maximilians-University (LMU) Munich, Technical University of Munich (Author)
  • Christina Lipp - , Technical University of Munich (Author)
  • Martina Rudelius - , Technical University of Munich (Author)
  • Alexander Zimmermann - , Technical University of Munich (Author)
  • Stefan Ockert - , Technical University of Munich (Author)
  • Hans Henning Eckstein - , Technical University of Munich (Author)
  • Jaroslav Pelisek - , Technical University of Munich (Author)

Abstract

An important feature of abdominal aortic aneurysm (AAA) is the destruction of vessel wall, especially elastin and collagen. Besides matrix metalloproteinases, cathepsins are the most potent elastolytic enzymes. The expression of cathepsins with known elastolytic and collagenolytic activities in the individual cells within AAA has not yet been determined. The vessel wall of 32 AAA patients and 10 organ donors was analysed by immunohistochemistry for expression of cathepsins B, D, K, L and S, and cystatin C in all cells localized within AAA. Luminal endothelial cells (ECs) of AAA were positive for cathepsin D and partially for cathepsins B, K and S. Endothelial cells of the neovessels and smooth muscle cells in the media were positive for all cathepsins tested, especially for cathepsin B. In the inflammatory infiltrate all cathepsins were expressed in the following pattern: B > D = S > K = L. Macrophages showed the highest staining intensity for all cathepsins. Furthermore, weak overall expression of cystatin C was observed in all the cells localized in the AAA with the exception of the ECs. There is markedly increased expression of the various cathepsins within the AAA wall compared to healthy aorta. Our data are broadly consistent with a role for cathepsins in AAA; and demonstrate expression of cathepsins D, B and S in phagocytic cells in the inflammatory infiltrate; and also may reveal a role for cathepsin B in lymphocytes.

Details

Original languageEnglish
Pages (from-to)252-258
Number of pages7
JournalInternational Journal of Experimental Pathology
Volume93
Issue number4
Publication statusPublished - Aug 2012
Peer-reviewedYes

External IDs

PubMed 22804761

Keywords

Keywords

  • Abdominal aortic aneurysm, Cathepsins, Cystatin C, Proteolytic degradation