Altered Storage and Function of von Willebrand Factor in Human Cardiac Microvascular Endothelial Cells Isolated from Recipient Transplant Hearts

• Published in: International journal of molecular sciences 2023-02, Vol.24 (5), p.4553
• Main Authors: Meli, Athinoula, McCormack, Ann, Conte, Ianina, Chen, Qu, Streetley, James, Rose, Marlene L, Bierings, Ruben, Hannah, Matthew J, Molloy, Justin E, Rosenthal, Peter B, Carter, Tom
• Format: Article
• Language: English
• Subjects: Biosynthesis; cardiac microvascular; Cardiomyopathy; Cardiovascular disease; Cells, Cultured; Chemical composition; Congestive heart failure; Dilated cardiomyopathy; Endothelial cells; Endothelial Cells - metabolism; Endothelium; Exocytosis; Fluorescence microscopy; Golgi apparatus; Heart diseases; Heart failure; Heart Failure - metabolism; Histamine; Humans; Industrial equipment and supplies industry; International economic relations; Kinases; Kinetics; Microvasculature; Morphology; Myosin; Oxidative stress; P-selectin; Physiology; Proteins; secretion; Synaptotagmin; t-Plasminogen activator; Tissue Plasminogen Activator - metabolism; Transplants & implants; Tubules; Ultrastructure; Von Willebrand factor; von Willebrand Factor - metabolism; Weibel–Palade body
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms24054553

The assembly of von Willebrand factor (VWF) into ordered helical tubules within endothelial Weibel-Palade bodies (WPBs) is required for the efficient deployment of the protein at sites of vascular injury. VWF trafficking and storage are sensitive to cellular and environmental stresses that are associated with heart disease and heart failure. Altered storage of VWF manifests as a change in WPB morphology from a rod shape to a rounded shape and is associated with impaired VWF deployment during secretion. In this study, we examined the morphology, ultrastructure, molecular composition and kinetics of exocytosis of WPBs in cardiac microvascular endothelial cells isolated from explanted hearts of patients with a common form of heart failure, dilated cardiomyopathy (DCM; HCMEC ), or from nominally healthy donors (controls; HCMEC ). Using fluorescence microscopy, WPBs in HCMEC (n = 3 donors) showed the typical rod-shaped morphology containing VWF, P-selectin and tPA. In contrast, WPBs in primary cultures of HCMEC (n = 6 donors) were predominantly rounded in shape and lacked tissue plasminogen activator (t-PA). Ultrastructural analysis of HCMEC revealed a disordered arrangement of VWF tubules in nascent WPBs emerging from the trans-Golgi network. HCMEC WPBs still recruited Rab27A, Rab3B, Myosin-Rab Interacting Protein (MyRIP) and Synaptotagmin-like protein 4a (Slp4-a) and underwent regulated exocytosis with kinetics similar to that seen in HCMECc. However, secreted extracellular VWF strings from HCMEC were significantly shorter than for endothelial cells with rod-shaped WPBs, although VWF platelet binding was similar. Our observations suggest that VWF trafficking, storage and haemostatic potential are perturbed in HCMEC from DCM hearts.