Endothelial Colony Forming Cells as an Autologous Model to Study Endothelial Dysfunction in Patients with a Bicuspid Aortic Valve
Autor: | Lidia R. Bons, Kirsten Lodder, Hans-Marc J. Siebelink, Kondababu Kurakula, Jolien W. Roos-Hesselink, Vera van de Pol, Marco C. DeRuiter, Marie-José Goumans, Gonzalo Sanchez-Duffhues |
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Přispěvatelé: | Physiology, ACS - Pulmonary hypertension & thrombosis, Cardiology |
Rok vydání: | 2019 |
Předmět: |
0301 basic medicine
Aortic valve Male endothelial colony forming cell blood outgrowth endothelial cell BOEC Heart Valve Diseases 030204 cardiovascular system & hematology migration lcsh:Chemistry calcification 0302 clinical medicine Bicuspid aortic valve Bicuspid Aortic Valve Disease Cell Movement Endothelial dysfunction lcsh:QH301-705.5 Spectroscopy Aorta Cells Cultured General Medicine Middle Aged Computer Science Applications medicine.anatomical_structure Aortic Valve Cardiology cardiovascular system Female Aortic valve calcification Dilatation Pathologic Adult medicine.medical_specialty bicuspid aortic valve Catalysis Article Inorganic Chemistry 03 medical and health sciences Young Adult Internal medicine medicine.artery ECFC medicine Humans Physical and Theoretical Chemistry Aortic rupture Molecular Biology Cell Size business.industry Organic Chemistry Endothelial Cells BAV medicine.disease aortic dilation 030104 developmental biology lcsh:Biology (General) lcsh:QD1-999 business Wound healing Calcification |
Zdroj: | International Journal of Molecular Sciences, Vol 20, Iss 13, p 3251 (2019) International Journal of Molecular Sciences, 20(13):3251. Multidisciplinary Digital Publishing Institute (MDPI) International Journal of Molecular Sciences Volume 20 Issue 13 International Journal of Molecular Sciences, 20(13). MDPI van de Pol, V, Bons, L R, Lodder, K, Kurakula, K B, Sanchez-Duffhues, G, Siebelink, H M J, Roos-Hesselink, J W, Deruiter, M C & Goumans, M J 2019, ' Endothelial colony forming cells as an autologous model to study endothelial dysfunction in patients with a bicuspid aortic valve ', International Journal of Molecular Sciences, vol. 20, no. 13, 3251 . https://doi.org/10.3390/ijms20133251 |
ISSN: | 1422-0067 1661-6596 |
DOI: | 10.3390/ijms20133251 |
Popis: | Bicuspid aortic valve (BAV), the most common congenital heart defect, is associated with an increased prevalence of aortic dilation, aortic rupture and aortic valve calcification. Endothelial cells (ECs) play a major role in vessel wall integrity. Little is known regarding EC function in BAV patients due to lack of patient derived primary ECs. Endothelial colony forming cells (ECFCs) have been reported to be a valid surrogate model for several cardiovascular pathologies, thereby facilitating an in vitro system to assess patient-specific endothelial dysfunction. Therefore, the aim of this study was to investigate cellular functions in ECFCs isolated from BAV patients. Outgrowth and proliferation of ECFCs from patients with BAV (n = 34) and controls with a tricuspid aortic valve (TAV, n = 10) were determined and related to patient characteristics. Interestingly, we were only able to generate ECFCs from TAV and BAV patients without aortic dilation, and failed to isolate ECFC colonies from patients with a dilated aorta. Analyzing EC function showed that while proliferation, cell size and endothelial-to-mesenchymal transition were similar in TAV and BAV ECFCs, migration and the wound healing capacity of BAV ECFCs is significantly higher compared to TAV ECFCs. Furthermore, calcification is blunted in BAV compared to TAV ECFCs. Our results reveal ECs dysfunction in BAV patients and future research is required to unravel the underlying mechanisms and to further validate ECFCs as a patient-specific in vitro model for BAV. |
Databáze: | OpenAIRE |
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