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Pneumocytes

Alveolar epithelium consists of three types of cells. Roughly 98 % of the alveolar surface is covered by squamous (type I) epithelial cells, from which thin sheets of cytoplasm extend to cover large areas of surface of even several alveoli (Haies et al. 1981). Type II epithelial cells, though more numerous but compact, occupy only 2 % of the alveolar surface. Type III cells, also called alveolar brush cells, are rare. [Pg.197]


Simon-Deckers, A. et al. (2008) In vitro investigation of oxide nanoparticle and carbon nanotube toxicity and intracellular accumulation in A549 human pneumocytes. Toxicology, 253 (1-3), 137-146. [Pg.211]

Complement (C3a, C5a) Macrophages, type II pneumocytes and fibroblasts Microbes Opsinization by phagocytes and chemotaxis Increased activity after exposure to LPS and allergens ozone, diesel, cigarette [23, 28]... [Pg.310]

It is commonly known that lipids, carbohydrates, and glycolipids are present in the Golgi apparatus (27). The determination of the components that react with the ZIO mixture was carried out by removing each component from tissues before incubation in the ZIO mixture. After lipid extraction by acetone (14), chloroform-methanol (15), or propylene oxide (27), no osmium-zinc precipitates could be detected in structures that normally reacted with ZIO. Blumcke et al. (15) summarized the nature of the lipids that react with the ZIO mixture as follows lipids and lipoproteins of cell membranes, neutral fat droplets (41), and lipid globules of type II pneumocytes and alveolar macrophages were, however, not as electron dense as the normally reactive lamellae containing highly unsaturated fatty acids. [Pg.237]

Blumcke WD, Kessler HR, Niedorf NH, Veith FJ. Ultrastructure of lamellar bodies of type II Pneumocytes after osmium-zinc impregnation. J Ultrastruct Res 1973 42 417-433. [Pg.246]

The cellular uptake appears to be a passive process, the cellular distribution being dependent on cell type. In cultured pneumocytes, the cell membrane was... [Pg.209]

Keywords Pneumocytes Pulmonary drug delivery Pulmonary metabolism, Alveolar epithelium... [Pg.258]

The human alveolar epithelium consists of two cell types type I (alveolar epithelial type I [ATI], pneumocyte I) and type n (alveolar epithelial type II... [Pg.259]

ATII cells, when plated on permeable supports or plastics under appropriate culture conditions, acquire features of type I cell-like phenotype and morphology [30, 57, 80], Although isolation of ATI pneumocytes from rat lungs has recently been reported with some success [28, 48, 81], development of confluent ATI cell monolayer with electrically tight characteristics has not been reported yet. It should be noted that unlike many other cells in primary culture, AEC exhibits generally a very limited proliferation profile and is therefore not suitable for passaging. Thus, a new preparation of cells has to be used for each data set, which drives the costs up tremendously, and a reliable normalisation scheme of data observed from each set of cell preparations is needed. [Pg.269]

Fehrenbach H, Schmiedl A, Wahlers T, Hirt SW, Brasch F, Riemann D, Richter J (1995) Morphometric characterisation of the fine structure of human type II pneumocytes. Anat Rec 243(1 ) 49-62... [Pg.275]

Kasper M, Reimann T, Hempel U, Wenzel KW, Bierhaus A, Schuh D, Dimmer V, Haroske G, Muller M (1998) Loss of caveolin expression in type I pneumocytes as an indicator of subcellular alterations during lung fibrogenesis. Histochem Cell Biol 109(1) 41—48... [Pg.276]

Bingle L, Bull TB, Fox B, Guz A, Richards RJ, Tetley TD (1990) Type II pneumocytes in mixed cell culture of human lung a light and electron microscopic study. Environ Health Perspect 85 71-80... [Pg.279]

Mamchaoui K, Makhloufi Y, Saumon G (2002) Glucose transporter gene expression in freshly isolated and cultured rat pneumocytes. Acta Physiol Scand... [Pg.280]

Gueven N, Glatthaar B, Manke HG, Haemmerle H (1996) Co-cultivation of rat pneumocytes and bovine endothelial cells on a liquid-air interface. Eur Respir J 9 968-975... [Pg.454]

Caveloae are particularly abundant, accounting for 30-70% of the plasma membrane in differentiated epithelial (e.g., pneumocytes) and endothelial cells, fibroblasts, smooth muscle cells, and adipocytes. Indeed there is a general trend for caveolin induction in differentiated cell types. Adipose tissue is replete with caveolae, and caveolin mRNA and protein are strongly induced during differentiation of 3T3-L1 preadipocytes (fibroblasts) to adipocytes [10], While... [Pg.601]

Chander A, Claypool WD Jr., Strauss JF III, Fisher AB. Uptake of liposomal phosphatidylcholine by granular pneumocytes in primary culture. Am J Physiol Cell Physiol 1983 245(5) 397-404. [Pg.380]

Rats exposed at 40 ppm 1 hour/day for periods of 7, 15, or 30 days had pulmonary irritation, parenchymal injury, and regenerative proliferation of pneumocytes, the severity of which depended on duration of exposure. [Pg.353]

In animals, acute oral exposure to doses of 4,000 mg/kg has been observed to cause respiratory edema, atelectasis and hemorrhage (Gould and Smuckler 1971). This is accompanied by marked disruption of subcellular structure in most pulmonary cell types, including granular pneumocytes, capillary endothelial cells and Clara cells (Boyd et al. 1980 Gould and Smuckler 1971 Hollinger 1982). It has been shown that Clara cells were most severely injured because they are the most active in metabolic activation of carbon tetrachloride. Injury to capillary endothelial cells is dose-... [Pg.51]

In many cell types it is feasible to deliver nucleic acids and genes by a variety of methods when the cells are grown in tissue culture (Table 58.1). Nonetheless, some cells, such as pneumocytes and neurons, are not readily isolated from humans and do not grow well in vitro. Furthermore, for many diseases it is essential to alter the phenotype of a significant proportion of the total cell population, making ex vivo gene therapy of limited use. [Pg.670]

Phospholipid that is the major component of Tung surfactant, and the syndrome caused by its deficiency Dipalmitoylphosphatidylcholine (DPPC, also called dipalmitoyllecithin, DPPL) is the major lipid component of lung surfactant. It is made and secreted by type II granular pneu-mocytes. Insufficient surfactant production causes respiratory distress syndrome, which can occur in preterm infants or adults whose surfactant-producing pneumocytes have been damaged or destroyed. [Pg.486]

A. K. Tanswell, D. M. Olson, and B. A. Freeman, Liposome-mediated augmentation of antioxidant defenses in fetal rat pneumocytes, Am. J. Physiol. 258 LI65 (1990). [Pg.89]

At the distal respiratory site, the alveolar epithelial cell layer is much flatter (0.1 -0.5 pm) and composed of two major cell types, squamous type I and agranular type II pneumocytes. Type I pneumocytes are non-phagocytic and highly flattened cells with broad and thin extensions. They occupy -95 % of the alveolar luminal surface, although they are less numerous than type II cells. The remaining surface is occupied by type II pneumocytes, which have blunt microvilli and contain multivesicular bodies [3, 11]. [Pg.214]

Type I pneumocytes, joined with endothelial cells by fused basement membranes, offer a very short airways-blood pathway for the diffusion of gases and drug molecules. They are known to contain numerous endocytotic vesicles which play an important role in the absorption process of proteins and transcellular movement of transporters [12, 13]. The functions of type II pneumocytes are well studied and include... [Pg.214]

Hydrophilic surfactant proteins A (SP-A) and D (SP-D), secreted by type II pneumocytes, interact specifically with a wide range of microorganisms and play important roles in the innate, natural defense system of the lung [16]. Both mRNA and protein levels of SP-A and SP-D increase dramatically in response to lung infection, injury and endotoxin challenge [17]. Type II pneumocytes also express class II major histocompatibility complex (MHC) antigens and intracellular adhesion molecule (ICAM-1), which may facilitate pulmonary immune responses [15]. [Pg.214]

Helliwell, P.A., D. Meredith, C.A. Boyd, J.R. Bronk, N. Lister, and P.D. Bailey. 1994. Tripeptide transport in rat lung. Biochim. Biophys. Acta 1190 430-434. Meredith, D., and C.A. Boyd. 1995. Dipeptide transport characteristics of the apical membrane of rat lung type II pneumocytes. Am.]. Physiol. 269 L137-L143. [Pg.237]


See other pages where Pneumocytes is mentioned: [Pg.331]    [Pg.162]    [Pg.100]    [Pg.148]    [Pg.360]    [Pg.309]    [Pg.60]    [Pg.338]    [Pg.260]    [Pg.269]    [Pg.269]    [Pg.274]    [Pg.603]    [Pg.378]    [Pg.331]    [Pg.353]    [Pg.276]    [Pg.354]    [Pg.202]    [Pg.216]    [Pg.216]    [Pg.217]    [Pg.137]    [Pg.95]    [Pg.404]    [Pg.214]    [Pg.221]   
See also in sourсe #XX -- [ Pg.272 , Pg.273 , Pg.274 , Pg.285 ]

See also in sourсe #XX -- [ Pg.172 , Pg.197 ]




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Nitric pneumocytes

Pneumocytes endoplasmic reticulum

Pneumocytes enzymes

Pneumocytes lamellar bodies

Pneumocytes multivesicular bodies

Pneumocytes surfactants

Type 1 pneumocytes

Type I Pneumocytes

Type II Pneumocytes

Type II pneumocyte

Type II pneumocyte hyperplasia

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