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Enzymes cell lumen release

Erosion of wood cell walls by soft rot fungi is less commonly reported. Hyphae growing in the cell lumen release enzymes that produce erosion patterns on the cell wall surface. These can take several forms including V-shaped nicks or smooth erosion troughs around the hypha, but in general, this type of attack is more prevalent in susceptible hardwoods than softwoods. [Pg.280]

The lysosomal enzymes The lysosomes are membrane vesicles ubiquitous to mammalian cells and contain a panoply of hydrolytic enzymes, estimated to be over 60 in number, that function to digest practically any biological macromolecule. They are important to the discussion of oral macromolecular drug delivery for two reasons. First, any macromolecules that escape digestion by the pancreatic and brush border enzymes are likely to be taken up into the epithelial cells by the process of endocytosis. In this process, the apical membrane invaginates and the target molecules enter endocytic vesicles that then fuse with the lysosomes and are subjected to intracellular hydrolysis by the lysosomal enzymes. Second, the sloughing-off of the epithelial cells means that the lysosomal enzymes will be released into the lumen of the intestine. They may be... [Pg.11]

Dietary proteins are cleaved to amino acids by proteases (see Fig. 2.2, circle 3). Pepsin acts in the stomach, and the proteolytic enzymes produced by the pancreas (trypsin, chymotrypsin, elastase, and the carboxypeptidases) act in the lumen of the small intestine. Aminopeptidases and di- and tripeptidases associated with the intestinal epithelial cells complete the conversion of dietary proteins to amino acids, which are absorbed into the intestinal epithelial cells and released into the hepatic portal vein. [Pg.24]

Figure 42-11. Model of iodide metabolism in the thyroid follicle. A follicular cell is shown facing the follicular lumen (top) and the extracellular space (at bottom). Iodide enters the thyroid primarily through a transporter (bottom left). Thyroid hormone synthesis occurs in the follicular space through a series of reactions, many of which are peroxidase-mediated. Thyroid hormones, stored in the colloid in the follicular space, are released from thyroglobulin by hydrolysis inside the thyroid cell. (Tgb, thyroglobulin MIT, monoiodotyrosine DIT, diiodotyro-sine Tj, triiodothyronine T4, tetraiodothyronine.) Asterisks indicate steps or processes that are inherited enzyme deficiencies which cause congenital goiter and often result in hypothyroidism. Figure 42-11. Model of iodide metabolism in the thyroid follicle. A follicular cell is shown facing the follicular lumen (top) and the extracellular space (at bottom). Iodide enters the thyroid primarily through a transporter (bottom left). Thyroid hormone synthesis occurs in the follicular space through a series of reactions, many of which are peroxidase-mediated. Thyroid hormones, stored in the colloid in the follicular space, are released from thyroglobulin by hydrolysis inside the thyroid cell. (Tgb, thyroglobulin MIT, monoiodotyrosine DIT, diiodotyro-sine Tj, triiodothyronine T4, tetraiodothyronine.) Asterisks indicate steps or processes that are inherited enzyme deficiencies which cause congenital goiter and often result in hypothyroidism.
It is postulated that chemotactic agents leach from respirable cotton dust particles in the small bronchioles. AECD recruit PMNs to the lung in the following sequence connective tissue beneath the basal lamina, between airway cells, and, finally, into the lumen. Chest tightness is also correlated with leucocyte recruitment (41). Although it has been proposed that extracellular lysosomal enzymes from PMNs cause the symptoms of byssinosis by initiating release of histamine and/or other chemical mediators (25), it has not been shown that cotton dust actually liberates hist j. jjfg m j y... [Pg.147]

Alternatively, the pro-drug may be a substrate for brush-border enzymes of the proximal tubular cell, resulting in release of the active drug in the tubular lumen and subsequent reabsorption at distal sites or elimination in the urine. [Pg.133]

Figure 7.33 The renal accumulation and toxicity of gentamycin (G). Gentamycin is filtered in the glomerulus and enters the tubular lumen. Here, it is taken up by proximal tubular cells and in vesicles as part of the uptake process. These fuse with lysosomes (L) inside the cell. The accumulation of gentamycin inside the lysosome destabilizes it, causing it to rupture and release its hydrolytic enzymes (o). These cause damage within the cell. Also, gentamycin can directly damage mitochondria (M). Figure 7.33 The renal accumulation and toxicity of gentamycin (G). Gentamycin is filtered in the glomerulus and enters the tubular lumen. Here, it is taken up by proximal tubular cells and in vesicles as part of the uptake process. These fuse with lysosomes (L) inside the cell. The accumulation of gentamycin inside the lysosome destabilizes it, causing it to rupture and release its hydrolytic enzymes (o). These cause damage within the cell. Also, gentamycin can directly damage mitochondria (M).
The best known functions of the ER require a high membrane surface and/or a separate, specific microenvironment within the organelle. Although many enzymes hosted by the ER use its membranous structure only as a scaffold, others are compartmentalized within the ER i.e., their active site is localized in the lumen. The activity of these enzymes usually is dependent on the special composition of the luminal compartment. The enzymes often receive their substrates and cofactors from or release their products to the cytosol therefore, the transport of these compounds across the ER membrane is indispensable. This article focuses on this latter group of the ER enzymes, the functioning of which makes the ER a separate metabolic compartment of the eukaryotic cell. [Pg.395]

The cephalic phase of digestion stimulates only a fraction of the maximum possible levels of gastric and pancreatic secretions. This phase does not seem to produce a rise in the levels of gastrin and CCK. Cephalic stimulation of the pancreas, as mediated by the vagus nerve, provokes release of pancreatic enzymes into the small intestine. Cephalic stimulation of the parietal cells, as mediated by the vagus nerve, provokes release of gastric acid into the lumen of the stomach- In humans, the cephalic phase does not seem to result in release of bicarbonate into the lumen of the small intestine. [Pg.67]

The chemical phase of digestion also involves the hormone cholecystokiiun (CCK). Dietary fats and proteins elicit the release of CCK from cells of the intes tines. The versatility of this hormone in digestion is revealed, later in this chapter, via studies involving dogs, rats, and humans. These studies address the influence of CCK on the release of pancreatic enzymes, bile salts, and pancreatic bicarbonate into the lumen of the small intestines-... [Pg.69]


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See also in sourсe #XX -- [ Pg.280 ]




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