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Macrophage alveolar

Damon, M., Cluzel, M., Chanez, P. and Goddard, P. (1989). Phagocytosis induction of chemiluminescence and chemoattractant-increased superoxide anion release from activated human alveolar macrophages in asthma. J. Biolumin. Chemolumin. 4, 279-286. [Pg.228]

Jaffe, H.A., Buhl, R., Borok, Z., Trapnell, B. and Crystal, R.G. (1989). Activated alveolar macrophages express increased levels of cytochrome b245 heavy chain mRNA transcripts correlating with enhanced capacity to release oxidants. Clin. Res. 37, 477A. [Pg.229]

Jordana, M., Richards, C., Irving, L.B. and Gauldie, J. (1988). Spontaneous in vitro release of alveolar macrophage cytokines after the intratracheal instillation of bleomycininrats. Am. Rev. Resp. Dis. 137, 1135-1140. [Pg.229]

Brown, G.M., Li, X.Y. and Donaldson, K. (1991a). Secretion of interleukin 1 and tumour necrosis fector by alveolar macrophages following exposure to particulate and fibrous dusts. In Mechanisms in Fibre Carcint nesis (eds. R.C. Brown, J.A. Hoskins and N.F. Johnson) pp. 499-504. Plenum, New York. [Pg.256]

Gabor, S., Anca, Z. and Zugravu, E. (1975). In vitro action of quartz on alveolar macrophage lipid peroxides. Arch. Environ. Health 30, 499-501. [Pg.258]

Hansen, K. and Mossman, B.T. (1987). Generation of superoxide (Oi ) from alveolar macrophages exposed to asbestiform and nonfibrous particles. Cancer Res. 47, 1681-1686. [Pg.258]

Hatch, G.E., Gardner, D.E. and Menzel, D.B. (1980). Stimulation of oxidant production in alveolar macrophages by pollutant and latex particles. Environ. Res. 23, 121-136. [Pg.258]

Nadeau, D., Lane, D.A., Paradis, D. and Fouquette, L. (1989). Effects of nicotinamide on the cytotoxicity of mineral dusts towards pulmonary alveolar macrophages. In Effects of Mineral Dusts on Cells (eds. B.T. Mossman and R.O. Begin) pp. 115-122. Springert Verlag, Berlin. [Pg.260]

Romert, L. and Jenssen, D. (1983). Rabbit alveolar macrophage-mediated mutagenesis of polycyclic aromatic hydrocarbons in V79 Chinese hamster cells. Mutat. Res. Ill, 245-252. [Pg.260]

A/J A Jackson inbred mouse strain ALP Anti-leukoprotease ALS Amyotrophic lateral sclerosis cAMP Cyclic adenosine monophosphate also known as adenosine 3, 5 -phosphate AM Alveolar macrophage AML Acute myelogenous leukaemia AMP Adenosine monophosphate AMVN 2,2 -azobis (2,4-dimethylvaleronitrile)... [Pg.279]

PAI Plasminogen activator inhibitor PA-IgG Platelet associated immunoglobulin G PAM Pulmonary alveolar macrophages... [Pg.285]

Local host defenses of both the upper and lower respiratory tract, along with the anatomy of the airways, are important in preventing infection. Upper respiratory defenses include the mucodliary apparatus of the nasopharynx, nasal hair, normal bacterial flora, IgA antibodies, and complement. Local host defenses of the lower respiratory tract include cough, mucodliary apparatus of the trachea and bronchi, antibodies (IgA, IgM, and IgG), complement, and alveolar macrophages. Mucus lines the cells of the respiratory tract, forming a protective barrier for the cells. This minimizes the ability of organisms to attach to the cells and initiate the infectious process. The squamous epithelial cells of the upper respiratory tract are not ciliated, but those of the columnar epithelium of the lower tract are. The cilia beat in a uniform fashion upward, moving particles up and out of the lower respiratory tract. [Pg.1050]


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See also in sourсe #XX -- [ Pg.106 ]




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Alveolar

Alveolar clearance macrophages

Alveolar macrophage clearance mechanisms

Alveolar macrophage function

Alveolar macrophage phagocytosis

Alveolar region, macrophages

Chemiluminescence, alveolar macrophage

Cytokines alveolar macrophages

Hamster alveolar macrophages

Macrophages alveolar, cytokine production

Neutrophils interaction with alveolar macrophages

Phagocytosis by alveolar macrophages

Pulmonary alveolar macrophages

Pulmonary alveolar macrophages PAMs)

Rabbit alveolar macrophages

Sarcoidosis alveolar macrophages

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