Chemiluminescence response of equine alveolar macrophages during stimulation with latex beads, or IgG-opsonized sheep red blood cells.
Abstract: Isolated equine alveolar macrophages were shown to generate a luminol-dependent light response when challenged with a phagocytic stimulus. The chemiluminescent response was not detected with luminol prepared at 1.0 x 10(-5) or 1.0 x 10(-4) molar concentrations, but was readily quantitated when used at a 1.0 x 10(-3) molar concentration. Challenge of the alveolar macrophages with latex particles or with equine IgG-coated sheep red blood cells elicited the luminol-dependent light response, whereas unchallenged equine alveolar macrophages or those challenged with unopsonized erythrocytes failed to emit light above background levels. Latex-bead-challenged macrophages released 8.06 times the total amount of light as those equine alveolar macrophages challenged with equine IgG-opsonized erythrocytes. This study represents the first investigation on chemiluminescence and equine alveolar macrophages.
Publication Date: 1983-06-01 PubMed ID: 6862592DOI: 10.1007/BF00917821Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
This research explores the light response of isolated horse lung cells when exposed to a phagocytic stimulus, providing groundbreaking insights on chemiluminescence and equine alveolar macrophages.
Chemiluminescent Response of Equine Alveolar Macrophages
- This study investigates the light-emitting response (chemiluminescence) of equine alveolar macrophages (a type of immune cell found in the lungs of horses) when stimulated with certain substances.
- These cells were isolated for the research and exposed to phagocytic stimulus, which promotes the process of phagocytosis, where cells engulf bacteria or other foreign substances to destroy them.
- The research found that equine alveolar macrophages generated a light response that is dependent on luminol, a chemical that exhibits chemiluminescence, glowing blue when mixed with an appropriate oxidizing agent.
Exposure to Different Stimulation
- The research involved testing the cells’ response with different molar concentrations of luminol, it was found that only 1.0 x 10(-3) molar concentration resulted in quantifiable light response. Lower concentrations did not lead to detectable chemiluminescence.
- The study also involved challenging the alveolar macrophages with latex particles or erythrocytes (red blood cells) coated with equine IgG, a type of antibody. The aim was to see if these stimuli would elicit the luminol-dependent light response.
- The cells did show a chemiluminescent response on challenge with both latex particles and IgG-coated erythrocytes. In contrast, unchallenged macrophages or those exposed to uncompromised erythrocytes did not produce light above background levels.
Comparative Light Emissions with Different Challenges
- The study looked into the comparative light emissions of alveolar macrophages when challenged with latex beads or IgG-opsonized erythrocytes. The findings showed that the macrophages released 8.06 times more light when challenged with latex beads compared to when challenged with erythrocytes coated with equine IgG.
- This indicates a greater chemiluminescent response when the macrophages deal with latex particles. However, the reasoning behind this outcome needs further exploration.
Significance of the Study
- This research is the first of its kind to study chemiluminescence in equine alveolar macrophages.
- The findings could have potential applications in the field of equine health, particularly related to immunological responses and potential diagnostic tools centering around chemiluminescence. Future studies can use these insights as a foundation to further understand the specific reactions of equine alveolar macrophages and their potential clinical implications.
Cite This Article
APA
Dyer RM, Leid RW.
(1983).
Chemiluminescence response of equine alveolar macrophages during stimulation with latex beads, or IgG-opsonized sheep red blood cells.
Inflammation, 7(2), 169-182.
https://doi.org/10.1007/BF00917821 Publication
Researcher Affiliations
MeSH Terms
- Animals
- Cells, Cultured
- Dose-Response Relationship, Drug
- Erythrocytes / immunology
- Horses
- Immunoglobulin G / immunology
- Latex / immunology
- Luminescent Measurements
- Luminol / pharmacology
- Macrophage Activation
- Macrophages / immunology
- Opsonin Proteins / immunology
- Pulmonary Alveoli / immunology
- Sheep
References
This article includes 40 references
- HANKS JH, WALLACE JH. Determination of cell viability.. Proc Soc Exp Biol Med 1958 May;98(1):188-92.
- Allen RC, Loose LD. Phagocytic activation of a luminol-dependent chemiluminescence in rabbit alveolar and peritoneal macrophages.. Biochem Biophys Res Commun 1976 Mar 8;69(1):245-52.
- Baehner RL, Murrmann SK, Davis J, Johnston RB Jr. The role of superoxide anion and hydrogen peroxide in phagocytosis-associated oxidative metabolic reactions.. J Clin Invest 1975 Sep;56(3):571-6.
- Holian A, Daniele RP. Stimulation of oxygen consumption and superoxide anion production in pulmonary macrophages by N-formyl methionyl peptides.. FEBS Lett 1979 Dec 1;108(1):47-50.
- SBARRA AJ, KARNOVSKY ML. The biochemical basis of phagocytosis. I. Metabolic changes during the ingestion of particles by polymorphonuclear leukocytes.. J Biol Chem 1959 Jun;234(6):1355-62.
- Root RK, Metcalf JA. H2O2 release from human granulocytes during phagocytosis. Relationship to superoxide anion formation and cellular catabolism of H2O2: studies with normal and cytochalasin B-treated cells.. J Clin Invest 1977 Dec;60(6):1266-79.
- Biggar WD, Buron S, Holmes B. Bactericidal mechanisms in rabbit alveolar macrophages: evidence against peroxidase and hydrogen peroxide bactericidal mechanisms.. Infect Immun 1976 Jul;14(1):6-10.
- Beall GD, Repine JE, Hoidal JR, Rasp FL. Chemiluminescence by human alveolar macrophages: stimulation with heat-killed bacteria or phorobol myristate acetate.. Infect Immun 1977 Jul;17(1):117-20.
- Ziprin RL. Phagocytosis by sheep alveolar macrophages: relationship between opsonin concentration and light emission in the presence of luminol.. Infect Immun 1978 Mar;19(3):889-92.
- Tsan MF. Stimulation of the hexose monophosphate shunt independent of hydrogen peroxide and superoxide production in rabbit alveolar macrophages during phagocytosis.. Blood 1977 Nov;50(5):935-45.
- Papermaster-Bender G, Whitcomb ME, Sagone AL Jr. Characterization of the metabolic responses of the human pulmonary alveolar macrophage.. J Reticuloendothel Soc 1980 Aug;28(2):129-39.
- Hoidal JR, Fox RB, Repine JE. Defective oxidative metabolic responses in vitro of alveolar macrophages in chronic granulomatous disease.. Am Rev Respir Dis 1979 Sep;120(3):613-8.
- Babior BM. Oxygen-dependent microbial killing by phagocytes (first of two parts).. N Engl J Med 1978 Mar 23;298(12):659-68.
- Root RK, Metcalf J, Oshino N, Chance B. H2O2 release from human granulocytes during phagocytosis. I. Documentation, quantitation, and some regulating factors.. J Clin Invest 1975 May;55(5):945-55.
- Andrew PW, Lowrie DB, Jackett PS, Peters TJ. Analytical subcellular fractionation of rabbit alveolar macrophages with particular reference to the subcellular localisation of pyridine nucleotide-dependent superoxide-generating systems and superoxide dismutase.. Biochim Biophys Acta 1980 Jan 11;611(1):61-71.
- Horton FO 3rd, McCallum RE, Rogers RM. Variable glucose metabolism in resting and phagocytizing human alveolar macrophages (HAM) measured by 14CO2 produced from glucose-1-14C.. Chest 1980 Feb;77(2 Suppl):315-8.
- Gee JB, Vassallo CL, Bell P, Kaskin J, Basford RE, Field JB. Catalase-dependent peroxidative metabolism in the alveolar macrophage during phagocytosis.. J Clin Invest 1970 Jun;49(6):1280-7.
- Romeo D, Zabucchi G, Soranzo M, Rossi F. Macrophage metabolism: activation of NADPH oxidation by phagocytosis.. Biochem Biophys Res Commun 1971 Nov;45(4):1056-62.
- Lew PD, Stossel TP. Effect of calcium on superoxide production by phagocytic vesicles from rabbit alveolar macrophages.. J Clin Invest 1981 Jan;67(1):1-9.
- Welch WD, Graham CW, Zaccari J, Thrupp LD. Analysis and comparison of the luminol-dependent chemiluminescence responses of alveolar macrophages and neutrophils.. J Reticuloendothel Soc 1980 Sep;28(3):275-83.
- OREN R, FARNHAM AE, SAITO K, MILOFSKY E, KARNOVSKY ML. Metabolic patterns in three types of phagocytizing cells.. J Cell Biol 1963 Jun;17(3):487-501.
- Goldstein IM, Roos D, Kaplan HB, Weissmann G. Complement and immunoglobulins stimulate superoxide production by human leukocytes independently of phagocytosis.. J Clin Invest 1975 Nov;56(5):1155-63.
- Forman HJ, Nelson J, Fisher AB. Rat alveolar macrophages require NADPH for superoxide production in the respiratory burst. Effect of NADPH depletion by paraquat.. J Biol Chem 1980 Oct 25;255(20):9879-83.
- DeChatelet LR, Mulikin D, McCall CE. The generation of superoxide anion by various types of phagocyte.. J Infect Dis 1975 Apr;131(4):443-6.
- Hoidal JR, Beall GD, Repine JE. Production of hydroxyl radical by human alveolar macrophages.. Infect Immun 1979 Dec;26(3):1088-92.
- Hoidal JR, Repine JE, Beall GD, Rasp FL Jr, White JG. The effect of phorbol myristate acetate on the metabolism and ultrastructure of human alveolar macrophages.. Am J Pathol 1978 Jun;91(3):469-82.
- Drath DB, Karnovsky ML. Superoxide production by phagocytic leukocytes.. J Exp Med 1975 Jan 1;141(1):257-62.
- Harrison JE, Schultz J. Studies on the chlorinating activity of myeloperoxidase.. J Biol Chem 1976 Mar 10;251(5):1371-4.
- Hoidal JR, Beall GD, Rasp FL Jr, Holmes B, White JG, Repine JE. Comparison of the metabolism of alveolar macrophages from humans, rats, and rabbits: phorbol myristate acetate.. J Lab Clin Med 1978 Nov;92(5):787-94.
- Cheson BD, Christensen RL, Sperling R, Kohler BE, Babior BM. The origin of the chemiluminescence of phagocytosing granulocytes.. J Clin Invest 1976 Oct;58(4):789-96.
- Vogt MT, Thomas C, Vassallo CL, Basford RE, Gee JB. Glutathione-dependent peroxidative metabolism in the alveolar macrophage.. J Clin Invest 1971 Feb;50(2):401-10.
- Reed PW. Glutathione and the hexose monophosphate shunt in phagocytizing and hydrogen peroxide-treated rat leukocytes.. J Biol Chem 1969 May 10;244(9):2459-64.
- Hatch GE, Gardner DE, Menzel DB. Stimulation of oxidant production in alveolar macrophages by pollutant and latex particles.. Environ Res 1980 Oct;23(1):121-36.
- Yamaguchi T, Kakinuma K, Kaneda M, Shimada K. Comparative studies on alveolar macrophages and polymorphonuclear leukocytes. I. H2O2 and O2- generation by rabbit alveolar macrophages.. J Biochem 1980 May;87(5):1449-55.
- Montarroso AM, Myrvik QN. Oxidative metabolism of BCG-activated alveolar macrophages.. J Reticuloendothel Soc 1979 Jun;25(6):559-74.
- Boxer LA, Ismail G, Allen JM, Baehner RL. Oxidative metabolic responses of rabbit pulmonary alveolar macrophages.. Blood 1979 Mar;53(3):486-91.
- Romeo D, Zabucchi G, Marzi T, Rossi F. Kinetic and enzymatic features of metabolic stimulation of alveolar and peritoneal macrophages challenged with bacteria.. Exp Cell Res 1973 Apr;78(2):423-32.
- Stokes SH, Davis WB, Sorber WA. Effect of phagocytosis on superoxide anion production and superoxide dismutase levels in BCG-activated and normal rabbit alveolar macrophages.. J Reticuloendothel Soc 1978 Aug;24(2):101-6.
- Westrick MA, Shirley PS, DeChatelet LR. Generation of chemiluminescence by human neutrophils exposed to soluble stimuli of oxidative metabolism.. Infect Immun 1980 Nov;30(2):385-90.
- Romeo D, Zabucchi G, Rossi F. Reversible metabolic stimulation of polymorphonuclear leukocytes and macrophages by concanavalin A.. Nat New Biol 1973 May 23;243(125):111-2.
Citations
This article has been cited 2 times.- Morton HC, Pleass RJ, Storset AK, Brandtzaeg P, Woof JM. Cloning and characterization of equine CD89 and identification of the CD89 gene in chimpanzees and rhesus macaques. Immunology 2005 May;115(1):74-84.
- Ansoborlo E, Chalabreysse J, Hengé-Napoli MH, Pujol E. In vitro chemical and cellular tests applied to uranium trioxide with different hydration states. Environ Health Perspect 1992 Jul;97:139-43.
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists