Comparison of cellular changes in cavalier King Charles spaniel and mixed breed dogs with myxomatous mitral valve disease

Chi-chien Lu, Mengmeng Liu, Geoffrey Culshaw, Anne French, Brendan Corcoran

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

The aim of this study was to determine if there are differences in cellular changes in cavalier King Charles spaniel (CKCS) myxomatous mitral valves compared to non-CKCS dogs.Animals: CKCSs (n=6) and age-matched mixed breed (n=6) with severe MMVD, and normal mixed breed (n=4) dogs.Methods: Immunohistochemistry staining and qualitative and quantitative analysis of mitral valves sections, examining for the presence of CD11c and CD45, vimentin, alpha smooth muscle actin (α-SMA) and myosin heavy chain 10 (Smemb), vonWillebrand factor (vWF) and CD31 and Ki-67. Results: Vimentin positive cell numbers were increased in the MMVD dogs and distributed throughout the valve with greatest density close to the endothelium. There were no significant differences in cell marker expression for the two diseased groups, but cell numbers were significantly increased compared to controls for α-SMA (CKCS only) and SMemb (CKCS and mixed breed) (P<0.05). α-SMA+ cells were primarily located at the valve edge, with Smemb+ cells similarly located, but also present throughout the valve stroma. A small number of cells close to the valve edge co-expressed α-SMA and SMemb. Endothelial vWF expression was identified in all valves, with evidence of disrupted endothelium in the diseased, but was also found in diseased valve stroma. There was no staining for CD11c, CD45 or CD31 in any valve. Ki-67+ cells formed linear clusters at the leaflet tip and were sparsely distributed throughout both myxomatous valve groups.Conclusions: The cellular changes notes with advanced stage MMVD are appear similar for CKCS when compared to mixed breed dogs.
Original languageEnglish
Pages (from-to)100-109
JournalJournal of Veterinary Cardiology
Issue number2
Early online date6 Feb 2016
Publication statusPublished - Jun 2016


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