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Czasopismo

2017 | 76 | 3 |

Tytuł artykułu

The expression of inhibitor of nuclear factor kappa-B kinase epsilon (IKKe) in human aortic aneurysm

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Background: Aortic aneurysm (AA) is one of the most common causes of sudden death among elderly people. Although AA can be detected by non-invasive imaging techniques, there are no pharmacological treatments currently available to prevent progression at any stage of the disease. In this study we will explore the expression of inhibitor of nuclear factor kappa-B kinase epsilon (IKKε) in AA and its potential underlying molecular mechanism in AA. Materials and methods: Human aortic tissue was taken from 14 patients who underwent surgical repair of AA for the AA group and another 11 patients with normal aorta who underwent aortic valve replacement surgery for the control group. After excision, we used haematoxylin-eosin staining, Masson staining, immunohistochemistry analysis and Western blot analysis to observe the expression, location and morphological changes of the IKKε, P50 and the extracellular matrix within the AA. Results: In the AA group, haematoxylin-eosin staining revealed a loss of medial integrity and inflammatory cell infiltration. Masson staining confirmed the degradation of the extracellular matrix in the AA group. Immunohistochemistry analysis showed increased infiltration of inflammatory cells and up-regulation of proinflammatory cytokines in the AA group when compared to the control group. Based on immunohistochemistry and Western blot analysis, there was clearly over-expression of IKKε, P50 and MMP2 in AA group, mainly in the intrinsic aortic cells of the media. Conclusions: The over-expression of IKKε may play an important role in the origination and progression of AA and might be a vital target for their treatment. (Folia Morphol 2017; 76, 3: 372–378)

Słowa kluczowe

Wydawca

-

Czasopismo

Rocznik

Tom

76

Numer

3

Opis fizyczny

p.372-378,fig.,ref.

Twórcy

autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China
autor
  • Department of Thoracic and Cardiovascular Surgery, Nanjing First Hospital, Nanjing Medical University, Jiangsu, People’s Republic of China

Bibliografia

  • 1. Cao C, Zhu Y, Chen W, et al. IKKepsilon knockout prevents high fat diet induced arterial atherosclerosis and NF-kB signaling in mice. PLoS One. 2013; 8(5): e64930, doi: 10.1371/journal.pone.0064930, indexed in Pubmed: 23741427.
  • 2. Cheuk BLY, Cheng SWK. Can local secretion of prostaglandin E2, thromboxane B2, and interleukin-6 play a role in ruptured abdominal aortic aneurysm? World J Surg. 2008; 32(1): 55–61, doi: 10.1007/s00268-007-9279-9, indexed in Pubmed: 17992560.
  • 3. Golledge J, Muller J, Daugherty A, et al. Abdominal aortic aneurysm: pathogenesis and implications for management. Arterioscler Thromb Vasc Biol. 2006; 26(12): 2605–2613, doi: 10.1161/01.ATV.0000245819.32762.cb, indexed in Pubmed: 16973970.
  • 4. Hinterseher I, Erdman R, Elmore JR, et al. Novel pathways in the pathobiology of human abdominal aortic aneurysms. Pathobiology. 2013; 80(1): 1–10, doi: 10.1159/000339303, indexed in Pubmed: 22797469.
  • 5. Jones KG, Brull DJ, Brown LC, et al. Interleukin-6 (IL-6) and the prognosis of abdominal aortic aneurysms. Circulation. 2001; 103(18): 2260–2265, indexed in Pubmed: 11342474.
  • 6. Kim YW, West XZ, Byzova TV. Inflammation and oxidative stress in angiogenesis and vascular disease. J Mol Med (Berl). 2013; 91(3): 323–328, doi:10.1007/s00109-013-1007-3, indexed in Pubmed: 23430240.
  • 7. Lenk GM, Tromp G, Weinsheimer S, et al. Whole genome expression profiling reveals a significant role for immune function in human abdominal aortic aneurysms. BMC Genomics. 2007; 8: 237, doi: 10.1186/1471-2164-8-237, indexed in Pubmed: 17634102.
  • 8. Löffek S, Schilling O, Franzke CW. Series “matrix metalloproteinases in lung health and disease”: Biological role of matrix metalloproteinases: a critical balance. Eur Respir J. 2011; 38(1): 191–208, doi: 10.1183/09031936.00146510, indexed in Pubmed: 21177845.
  • 9. Nagase H, Visse R, Murphy G. Structure and function of matrix metalloproteinases and TIMPs. Cardiovasc Res. 2006; 69(3): 562–573, doi:10.1016/j.cardiores.2005.12.002, indexed in Pubmed: 16405877.
  • 10. Rohde LE, Arroyo LH, Rifai N, et al. Plasma concentrations of interleukin-6 and abdominal aortic diameter among subjects without aortic dilatation. Arterioscler Thromb Vasc Biol. 1999; 19(7): 1695–1699, indexed in Pubmed: 10397687.
  • 11. Svensjö S, Björck M, Gürtelschmid M, et al. Low prevalence of abdominal aortic aneurysm among 65-year-old Swedish men indicates a change in the epidemiology of the disease. Circulation. 2011; 124(10): 1118–1123, doi: 10.1161/CIRCULATIONAHA.111.030379, indexed in Pubmed: 21844079.
  • 12. Thompson RW. Reflections on the pathogenesis of abdominal aortic aneurysms. Cardiovasc Surg. 2002; 10(4): 389–394, indexed in Pubmed:12359414.
  • 13. Tsai SH, Huang PH, Peng YJ, et al. Zoledronate attenuates angiotensin II-induced abdominal aortic aneurysm through inactivation of Rho/ROCK-dependent JNK and NF-kappaB pathway. Cardiovasc Res. 2013; 100(3): 501–510, doi: 10.1093/cvr/cvt230, indexed in Pubmed: 24225494.
  • 14. Verhelst K, Verstrepen L, Carpentier I, et al. IkappaB kinase epsilon (IKKepsilon): a therapeutic target in inflammation and cancer. Biochem Pharmacol. 2013; 85(7): 873–880, doi: 10.1016/j.bcp.2013.01.007, indexed in Pubmed: 23333767.
  • 15. Yamashita O, Yoshimura K, Nagasawa A, et al. Periostin links mechanical strain to inflammation in abdominal aortic aneurysm. PLoS One. 2013; 8(11): e79753, doi: 10.1371/journal.pone.0079753, indexed in Pubmed: 24260297.
  • 16. Yoshimura K, Aoki H. Recent advances in pharmacotherapy development for abdominal aortic aneurysm. Int J Vasc Med. 2012; 2012: 648167, doi:10.1155/2012/648167, indexed in Pubmed: 22957259.

Typ dokumentu

Bibliografia

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Identyfikator YADDA

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