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Secretion Golgi apparatus

Golgi apparatus A system of flattened membrane-bounded vesicles often stacked into a complex. Numerous small vesicles are found peripheral to the Golgi and contain secretory material packaged by the Golgi. Involved in the packaging and processing of macromolecules for secretion and for delivery to other cellular compartments. [Pg.27]

Histamine is a critical mediator in anaphylactic reactions. It is a diamine produced by decarboxylation of the amino acid histidine in the Golgi apparatus of mast cells and basophils. Once secreted, it is rapidly metabolized by histamine methyltransferase [2]. Plasma histamine levels are elevated in anaphylaxis, reaching a concentration peak at 5 min and declining to baseline by 30-60 min [3]. Therefore, histamine samples for assessing an anaphylactic reaction should be obtained within 15 min of the onset of the reaction. Urinary metabolites of histamine may be found for up to 24 h. [Pg.126]

Figure 25-2. The formation and secretion of (A) chylomicrons by an intestinal cell and (B) very low density lipoproteins by a hepatic cell. (RER, rough endoplasmic reticulum SER, smooth endoplasmic reticulum G, Golgi apparatus N, nucleus C, chylomicrons VLDL, very low density lipoproteins E, endothelium SD, space of Disse, containing blood plasma.) Apolipoprotein B, synthesized in the RER, is incorporated into lipoproteins in the SER, the main site of synthesis of triacylglycerol. After addition of carbohydrate residues in G, they are released from the cell by reverse pinocytosis. Chylomicrons pass into the lymphatic system. VLDL are secreted into the space of Disse and then into the hepatic sinusoids through fenestrae in the endothelial lining. Figure 25-2. The formation and secretion of (A) chylomicrons by an intestinal cell and (B) very low density lipoproteins by a hepatic cell. (RER, rough endoplasmic reticulum SER, smooth endoplasmic reticulum G, Golgi apparatus N, nucleus C, chylomicrons VLDL, very low density lipoproteins E, endothelium SD, space of Disse, containing blood plasma.) Apolipoprotein B, synthesized in the RER, is incorporated into lipoproteins in the SER, the main site of synthesis of triacylglycerol. After addition of carbohydrate residues in G, they are released from the cell by reverse pinocytosis. Chylomicrons pass into the lymphatic system. VLDL are secreted into the space of Disse and then into the hepatic sinusoids through fenestrae in the endothelial lining.
PDI contains a C-terminal tetrapeptide sequence known as the endoplasmic retention signal, KDEL. This anchor mediates the interaction between plasma membrane and membranes of the Golgi apparatus via a KDEL receptor. The PDI KDEL receptor complex is recycled back into the endoplasmic reticulum (Xiao et al., 1999). It is thought that a saturation of the retention mechanism results in the secretion of PDI which is deposited on the cell membrane and stabilized by electrostatic interactions (Terada et al, 1995). The secreted PDI is termed cell surface PDI (csPDI)... [Pg.101]

Lysosomal enzymes are glycosylated and modified in a characteristic way. Most importantly, when they arrive in the Golgi apparatus, specific mannose residues in their oligosaccharide chains are phosphorylated. This phosphorylation is the critical event that removes them Corn the secretion pathway and directs them to lysosomes. Genetic defects affecting this phosphorylation produce I-ceU disease in which lysosomal enzymes are released into the ejctracellular space, and inclusion bodies accumulate in the cell, compromising its function. [Pg.57]

Many proteins on the surface of the plasma membrane, and the majority of secreted proteins, contain oligosaccharide residues that are post-translationally added to the endoplasmic reticulum and in the Golgi apparatus (see p.230). By contrast, cytoplasmic proteins are rarely glycosylated. Glycoproteins can contain more than 50% carbohydrate however, the proportion of protein is generally much greater. [Pg.44]

Brown, R. M., Herth, W., Franke, W. W., Romanovicz, D. The role of the Golgi apparatus in the biosynthesis and secretion of a cellulosic glycoprotein in Pleurochrysis a model system for the synthesis of structural polysaccharides. In Biogenesis of plant cell wall polysaccharides, pp. 207. Loewus, F. (ed.). New York Academic Press 1973... [Pg.142]

SG, secretion granule V, vacuole Nu, nucleolus G, Golgi apparatus CW, cell wall (of a plant)... [Pg.10]

These secretion granules move to the surface and are released from the cell. In this process of exocytosis the membranes surrounding the granules fuse with the outer cell membrane. The rough ER appears to contribute membrane material to the smooth ER and Golgi apparatus, while material from Golgi membranes can become incorporated into the outer cell membrane and into lysosomes. Outer mitochondrial membranes and membranes around vacuoles in plant cells may also be derived directly from the ER. Outer membrane materials are probably "recycled" by endocytosis. [Pg.14]

Figure 20-8 (A) Electron micrograph showing a transverse section through part of the Golgi apparatus of an early spermatid. Cistemae of the ER, Golgi stacks (S), and vesicles (V) can be seen. Curved arrows point to associated tubules. Magnification X45/000.276 Courtesy of Y. Clermont. (B) Scheme showing functions of endoplasmic reticulum, transfer vesicles, Golgi apparatus, and secretion vesicles in the metabolism of glycoproteins. Figure 20-8 (A) Electron micrograph showing a transverse section through part of the Golgi apparatus of an early spermatid. Cistemae of the ER, Golgi stacks (S), and vesicles (V) can be seen. Curved arrows point to associated tubules. Magnification X45/000.276 Courtesy of Y. Clermont. (B) Scheme showing functions of endoplasmic reticulum, transfer vesicles, Golgi apparatus, and secretion vesicles in the metabolism of glycoproteins.

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See also in sourсe #XX -- [ Pg.146 ]




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Golgi apparatus

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