“…In some instances, these deposited blood cells from the circulating blood are soon replaced by migrating and spreading endogenous endothelium. In other instances, colonies of replicating endothelial cells grow on the exposed area but fail to completely repopulate the monolayer and with time these areas of exposed basement membrane develop a fibrous and nonthrombogenic covering (Berger et al 1972;Herring et al 1984;Clowes et al 1985Clowes et al , 1986Zilla et al 1994Zilla et al , 2007. Thus, the extent and type of vascular intima repair or regeneration is perhaps dependent on the extent and type of injury or implant and perhaps the age of the host.…”
Section: Blood Vessel Formation Repair and Remodeling Are Regulatedmentioning
“…In some instances, these deposited blood cells from the circulating blood are soon replaced by migrating and spreading endogenous endothelium. In other instances, colonies of replicating endothelial cells grow on the exposed area but fail to completely repopulate the monolayer and with time these areas of exposed basement membrane develop a fibrous and nonthrombogenic covering (Berger et al 1972;Herring et al 1984;Clowes et al 1985Clowes et al , 1986Zilla et al 1994Zilla et al , 2007. Thus, the extent and type of vascular intima repair or regeneration is perhaps dependent on the extent and type of injury or implant and perhaps the age of the host.…”
Section: Blood Vessel Formation Repair and Remodeling Are Regulatedmentioning
“…However, numerous studies using traditional staining methods, isotopes, and electron microscopy (7)(8)(9) as well as recent studies using new imaging techniques (1,2) have not detected platelets on the surface of fibrin. Moreover, previous reports have documented that the surface of implanted vascular grafts, which is exposed to flowing blood and invariably coated with fibrin, remains acellular over the years after implantation (10). The anti-adhesive mechanisms that protect the fibrin cap of hemostatic clots and the lumenal fibrin of implanted biomaterials from the excessive accumulation of blood cells in vivo are poorly understood.…”
Background: Surface-induced aggregation of fibrinogen results in the assembly of an extensible multilayered matrix, which prevents integrin-mediated cell adhesion. Results: Without the ␣C regions, the fibrinogen molecules assemble a defective, poorly extensible matrix supporting sustained cell adhesion.
Conclusion:The assembly of nonadhesive fibrinogen multilayer requires the ␣C regions of the molecule. Significance: The molecular mechanism for the assembly of the fibrinogen multilayer is identified.
“…24 Spontaneous EC ingrowth or ''in situ endothelialization'' rarely occurs in humans on prosthetic grafts. 25 Therefore, a goal for tissue engineered grafts is to produce a lumenal surface that is both resistant to platelet aggregation and favorable for EC regrowth. The flow chamber allows a temporal observation of EC proliferation and morphological adaptation to SS in situ.…”
In the development of engineered vascular grafts, assessing the material's interactive properties with peripheral blood cells and its capacity to endothelialize are important for predicting in vivo graft behavior. Current in vitro techniques used for characterizing cell adhesion at the surface of engineered scaffolds under flow only facilitate a terminal quantification of cell/surface interactions. Here, we present the design of an innovative flow chamber for real-time analysis of blood-biomaterial interactions under controllable hemodynamic conditions. Decellularized human umbilical veins (dHUV) were used as model vascular allografts to characterize platelet, leukocyte, and endothelial cell (EC) adhesion dynamics. Confluent EC monolayers adhered to the lumenal surface of the grafting material were flow conditioned to resist arterial shear stress levels (up to 24 dynes/cm 2 ) over a 48 h period, and shown to maintain viability over the 1 week assessment period. The basement membrane was imaged while whole blood/neutrophil suspensions were perfused across the HUV surface to quantify cell accumulation. This novel method facilitates live visualization of dynamic events, including cell adhesion, migration, and morphological adaptation at the blood-graft interface on opaque materials, and it can be used for preliminary assessment of clinically relevant biomaterials before implantation.
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