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Glycoproteins adhesive

Other blood-tissue barriers (e.g., blood-thymus, blood-testis) are less well defined [55,56]. An air-blood barrier also has been described that affects the systemic uptake of aerosolized molecules [57]. Therapeutants that target glycoprotein adhesion molecules on endothelium might surmount the blood-brain or other tissue barriers [58]. [Pg.247]

Collagen is a major component of connective tissue that becomes exposed at the subendothelium of injured blood vessels. It contributes to platelet adhesion and also plays a role in platelet activation by binding to several receptors on platelets such as integrin a 2(3 1 or glycoprotein VI (GP VI). [Pg.381]

The von Willebrand factor (vWf) is a heterogeneous multimeric plasma glycoprotein produced by megakaryocytes and endothelial cells which is found in platelets, plasma and the subendothelium. Subendothelial vWf facilitates platelet adhesion, especially under high shear stress, by binding to glycoprotein GPIb-V-IX, a complex of four leucine-rich repeat proteins on platelets. [Pg.1313]

HK it can interact with surface-bound factor XII on an adjacent particle thereby disseminating the reaction [25, 28]. As a result the effective kallikrein/factor XII ratio is increased in the presence of HK [25], Finally, in plasma, HK can displace other adhesive glycoproteins such as fibrinogen from binding to the surface [29]. In this sense, HK, like factor XII and prekallikrein, is also a coagulation cofactor because it is required for the generation of kalUkrein (a factor XII activator) as well as the activation of factor XI. [Pg.72]

FIBRONECTIN IS AN IMPORTANT GLYCOPROTEIN INVOLVED IN CELL ADHESION MIGRATION... [Pg.540]

Glycoprotein llb/llla Platelets allbps ICAM-2 Fibrinogen, fibronectin, von Willebrand factor Platelet adhesion and aggregation... [Pg.622]

At cellular level each stage of atheroma development is accompanied by the expression of specific glycoproteins by endothelial cells which mediate the adhesion of monocytes and T-lymphocytes. Their recruitment and migration is triggered by various cytokines released by leukocytes and possibly by smooth muscle cells. Atheroma development continues with the activation of macrophages, which accumulate lipids and become, together with lymphocytes, so-called fatty streaks. The continuous influx, differentiation and proliferation finally leads to more advanced lesion and to the formation of the fibrous plaque. ... [Pg.6]

Fig. 4.6(a) Migration of LHRH neurocrine cells prenatal transportation along the track of extra-bulbar VN axons (caudal branch). CB, cribriform plate FB, forebrain cell types, TAG-1, transient axonal surface glycoprotein and N-CAM, neural cell adhesion molecule (from Yoshida et al, 1995). [Pg.88]

Von Willebrand factor (VWF) is a large multimeric glycoprotein with two main functions in hemostasis to aid the platelet adhesion to injured blood vessel walls and to carry and stabilize factor VIII in plasma. Table 64—4 represents three main vWD phenotypes, their frequency, and genetic transmission.17... [Pg.992]

Fig. 1. Surface phenotype of HSPCs. Primitive HSPCs have the phenotype of c-KitThy-ll0WLin CD34+CD33 in humans, and the mouse counterparts have the phenotype of c-KifThy-llowLin Sca-l+. Primitive HSPCs express CXCR4 as the major chemokine receptor and various adhesion molecules such as VLA-4, VLA-5, LFA-1, P-selectin glycoprotein ligand-1 (PSGL-1), and CD44 for migration to the stem cell niche. Fig. 1. Surface phenotype of HSPCs. Primitive HSPCs have the phenotype of c-KitThy-ll0WLin CD34+CD33 in humans, and the mouse counterparts have the phenotype of c-KifThy-llowLin Sca-l+. Primitive HSPCs express CXCR4 as the major chemokine receptor and various adhesion molecules such as VLA-4, VLA-5, LFA-1, P-selectin glycoprotein ligand-1 (PSGL-1), and CD44 for migration to the stem cell niche.
Thus, while glycoprotein Ia/IIa (a2Pj) binds to collagen, glycoprotein Ic/IIa (a ) binds to fibronectin (5). The other integrin belonging to the beta 1 family that is involved in platelet adhesion is ct6P, which binds laminin. [Pg.135]

Tandon N. N Kralisz U, Jamieson G. A. Identification of glycoprotein IV (CD36) as a primary receptor for platelet collagen adhesion. J Biol Chem 1989 264,7576-83. [Pg.163]

It has been shown that cell adhesion highly depends on the outermost functional groups on SAMs however, cells do not directly interact with the SAMs. Instead, they interact with proteins adsorbed on SAMs. Cell adherence requires an interaction between integral molecules in the cell membrane and glycoproteins specialized for cell adhesion, like fibronectin (Fn) and vitronectin (Vn), which are adsorbed on the artificial material. Thus, the presence of glycoproteins in serum plays a crucial role in cell adherence to artificial materials. In the first part of this review (Sect. 2), we will briefly survey recent studies of cell adhesion on SAMs with different functional groups and discuss the mechanisms involved. [Pg.168]

Knowledge gained from cell adhesion studies with SAMs has been used to develop culture substrates with the appropriate cell adhesion glycoproteins for different types of cells [7-10], Stem cells, capable of self-renewal and differentiation into multiple cell types, are found in embryonic and adult tissues. Pluripotent stem cells, like embryonic stem cells and induced pluripotent stem cells, have been developed in vitro. These cells are expected to provide cell sources for regenerative medicine. Various culture conditions have been developed to enable expansion of these cells without loss of their multi- and pluripotency and to induce differentiation into viable cells with specific functions. [Pg.169]


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