Augmentation of rat alveolar macrophage migration by surfactant protein. 1987

R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber

Since the alveolar macrophage (AM) resides in an environment made unique by the presence of pulmonary surfactant, we studied the effect of constituents of pulmonary surfactant on the migration of these cells in vitro. Whole pulmonary surfactant, surfactant phospholipids, and a delipidated preparation of surfactant consisting mainly of protein were tested for their effect on AM migration. Migration was measured in multiwell chemotaxis chambers with endotoxin-activated rat serum (EARS) as the stimulus. The delipidated surfactant material (DSM) markedly augmented the migration of rat AM. Enhancement was seen only when migration was stimulated with EARS. Augmentation of stimulated migration occurred over a wide range of protein concentrations in DSM (3.5 to 56 micrograms/ml) in a dose-dependent fashion. Rat AM that were preincubated with DSM and then tested in the chemotaxis assay without DSM showed increased migration towards EARS when compared with AM preincubated in buffer alone. The enhancing effect of DSM on AM migration was significantly diminished by heating the DSM and by enzymatic digestion with trypsin, suggesting that the active constituent in DSM was protein. Thus, it appears that proteins isolated from pulmonary surfactant augment the stimulated migration of AM via an interaction between the protein and the macrophage. Although the identity of these proteins remains to be elucidated, it is unlikely they include albumin since purified rat serum albumin in concentrations comparable to that of protein in DSM did not enhance the stimulated migration of AM. These results represent further confirmation that constituents of surfactant modulate the clearance function of AM in vitro. Thus, it is likely that surfactant plays a role in lung defense mediated by AM.

UI MeSH Term Description Entries
D008264 Macrophages The relatively long-lived phagocytic cell of mammalian tissues that are derived from blood MONOCYTES. Main types are PERITONEAL MACROPHAGES; ALVEOLAR MACROPHAGES; HISTIOCYTES; KUPFFER CELLS of the liver; and OSTEOCLASTS. They may further differentiate within chronic inflammatory lesions to EPITHELIOID CELLS or may fuse to form FOREIGN BODY GIANT CELLS or LANGHANS GIANT CELLS. (from The Dictionary of Cell Biology, Lackie and Dow, 3rd ed.) Bone Marrow-Derived Macrophages,Monocyte-Derived Macrophages,Macrophage,Macrophages, Monocyte-Derived,Bone Marrow Derived Macrophages,Bone Marrow-Derived Macrophage,Macrophage, Bone Marrow-Derived,Macrophage, Monocyte-Derived,Macrophages, Bone Marrow-Derived,Macrophages, Monocyte Derived,Monocyte Derived Macrophages,Monocyte-Derived Macrophage
D008297 Male Males
D011510 Proteolipids Protein-lipid combinations abundant in brain tissue, but also present in a wide variety of animal and plant tissues. In contrast to lipoproteins, they are insoluble in water, but soluble in a chloroform-methanol mixture. The protein moiety has a high content of hydrophobic amino acids. The associated lipids consist of a mixture of GLYCEROPHOSPHATES; CEREBROSIDES; and SULFOGLYCOSPHINGOLIPIDS; while lipoproteins contain PHOSPHOLIPIDS; CHOLESTEROL; and TRIGLYCERIDES.
D011650 Pulmonary Alveoli Small polyhedral outpouchings along the walls of the alveolar sacs, alveolar ducts and terminal bronchioles through the walls of which gas exchange between alveolar air and pulmonary capillary blood takes place. Alveoli, Pulmonary,Alveolus, Pulmonary,Pulmonary Alveolus
D011663 Pulmonary Surfactants Substances and drugs that lower the SURFACE TENSION of the mucoid layer lining the PULMONARY ALVEOLI. Surfactants, Pulmonary,Pulmonary Surfactant,Surfactant, Pulmonary
D011919 Rats, Inbred Strains Genetically identical individuals developed from brother and sister matings which have been carried out for twenty or more generations or by parent x offspring matings carried out with certain restrictions. This also includes animals with a long history of closed colony breeding. August Rats,Inbred Rat Strains,Inbred Strain of Rat,Inbred Strain of Rats,Inbred Strains of Rats,Rat, Inbred Strain,August Rat,Inbred Rat Strain,Inbred Strain Rat,Inbred Strain Rats,Inbred Strains Rat,Inbred Strains Rats,Rat Inbred Strain,Rat Inbred Strains,Rat Strain, Inbred,Rat Strains, Inbred,Rat, August,Rat, Inbred Strains,Rats Inbred Strain,Rats Inbred Strains,Rats, August,Rats, Inbred Strain,Strain Rat, Inbred,Strain Rats, Inbred,Strain, Inbred Rat,Strains, Inbred Rat
D002465 Cell Movement The movement of cells from one location to another. Distinguish from CYTOKINESIS which is the process of dividing the CYTOPLASM of a cell. Cell Migration,Locomotion, Cell,Migration, Cell,Motility, Cell,Movement, Cell,Cell Locomotion,Cell Motility,Cell Movements,Movements, Cell
D002633 Chemotaxis The movement of cells or organisms toward or away from a substance in response to its concentration gradient. Haptotaxis
D000818 Animals Unicellular or multicellular, heterotrophic organisms, that have sensation and the power of voluntary movement. Under the older five kingdom paradigm, Animalia was one of the kingdoms. Under the modern three domain model, Animalia represents one of the many groups in the domain EUKARYOTA. Animal,Metazoa,Animalia
D051381 Rats The common name for the genus Rattus. Rattus,Rats, Laboratory,Rats, Norway,Rattus norvegicus,Laboratory Rat,Laboratory Rats,Norway Rat,Norway Rats,Rat,Rat, Laboratory,Rat, Norway,norvegicus, Rattus

Related Publications

R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
April 1993, The American journal of physiology,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
September 2002, Journal of immunology (Baltimore, Md. : 1950),
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
January 2004, American journal of physiology. Lung cellular and molecular physiology,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
February 2001, Journal of immunology (Baltimore, Md. : 1950),
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
June 1997, Respirology (Carlton, Vic.),
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
January 2022, Frontiers in immunology,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
November 1994, Histochemistry,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
August 1992, The Biochemical journal,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
April 1999, American journal of respiratory cell and molecular biology,
R M Hoffman, and W D Claypool, and S L Katyal, and G Singh, and R M Rogers, and J H Dauber
July 1993, Nihon Kyobu Shikkan Gakkai zasshi,
Copied contents to your clipboard!