Key result
Mechanical stress induced superimposed tissue formation in an ex vivo mitral valve model, with no significant correlation between original leaflet and superimposed tissue thickness (r = -0.27, P=0.23).
Why the study?
In mitral valve prolapse, leaflet thickening involves superimposed tissue formation, but the mechanisms underlying its formation were unknown.
Mechanical stress induces specific cellular and molecular changes resulting in superimposed tissue formation in mitral valves, providing insights into the mechanisms of mitral valve prolapse.
Answers are grounded in this paper and cite their sources.
Mechanical stress may drive mitral valve remodeling independent of baseline thickness; leaves open in vivo validation and clinical relevance.
AIMS: In mitral valve prolapse (MVP), leaflet thickening has recently been suggested to be due, in addition to a myxomatous degeneration, to the presence of a superimposed tissue (SIT), defined as an additional fibrous layer on top of the original leaflet. The mechanisms of SIT formation are currently unknown. We hypothesized that SIT formation would result from excessive leaflet stress and we used a unique ex vivo model to assess the correlation between leaflet remodelling and the type and location of mechanical stress and to elucidate the mechanisms underlying SIT formation. METHODS AND RESULTS: Human diseased mitral valves (MVs; n = 21) were histologically analysed for SIT formation and original leaflet thickening. The SIT comprised of various compositions of extracellular matrix and could reach more than 50% of total leaflet thickness. Original leaflet and SIT thickness did not show significant correlation (r = -0.27, P = 0.23), suggesting different regulatory mechanisms. To study the role of the mechanical environment on MV remodelling, mouse MV were cultured in their natural position in the heart and subjected to various haemodynamic conditions representing specific phases of the cardiac cycle and the MVP configuration. SIT formation was induced in the ex vivo model, mostly present on the atrial side, and clearly dependent on the duration, type, and extent of mechanical stress. Specific stainings and lineage tracing experiments showed that SIT comprises of macrophages and myofibroblasts and is associated with the activation of the transforming growth factor-beta and bone morphogenetic protein signalling pathways. Migration of valvular interstitial cells and macrophages through breakages of the endothelial cell lining contributed to SIT formation. CONCLUSIONS: Mechanical stresses induce specific cellular and molecular changes in the MV that result in SIT formation. These observations provide the first insights in the mechanism of SIT formation and represent an initial step to identify potential novel and early treatment for MVP.
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Kruithof et al. (2019) studied Mitral valve prolapse (n=21). Mechanical stress was evaluated on Correlation between original leaflet and superimposed tissue thickness (r = -0.27, p=0.23). Mechanical stress induced superimposed tissue formation in an ex vivo mitral valve model, with no significant correlation between original leaflet and superimposed tissue thickness (r = -0.27, P=0.23).
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