DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES
We investigated direct effects of granulocyte-macrophage colony-stimulating factor (GM-CSF) on the surface properties and cytokine-producing activity of human monocytes/macrophages (Mc/Mphs). The CD14+ cells were isolated from peripheral blood of healthy donors by positive magnetic separation. The i...
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oai:doaj.org-article:46a92220f2b642c68919e3a8ea2bf1442021-11-18T08:03:48ZDIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES1563-06252313-741X10.15789/1563-0625-2019-3-419-426https://doaj.org/article/46a92220f2b642c68919e3a8ea2bf1442019-07-01T00:00:00Zhttps://www.mimmun.ru/mimmun/article/view/1815https://doaj.org/toc/1563-0625https://doaj.org/toc/2313-741XWe investigated direct effects of granulocyte-macrophage colony-stimulating factor (GM-CSF) on the surface properties and cytokine-producing activity of human monocytes/macrophages (Mc/Mphs). The CD14+ cells were isolated from peripheral blood of healthy donors by positive magnetic separation. The isolated Mc/Mphs were cultured with lipopolysaccharide (LPS, 1 μg/ml) or without LPS for 24 hours. Membrane expression of CD14, CD16, CD119, CD124, and CD197 molecules was assessed by flow cytometry. The contents of tumor necrosis factor-α (TNFα), interleukin-1β (IL-1β), IL-6 and IL-10 in culture supernatants were determined by the enzyme immunoassay technique. It was found that GM-CSF at a concentration range of 0.01-10 ng/ml did significantly reduce the number of cells expressing CD197 (CC receptor of chemokine 7), without significantly affecting the percentage of CD14+ (coreceptor of LPS), CD16+ (low-affinity Fc receptor), CD119+ (IFNγ receptor) and CD124+ (IL-4 receptor) cells. At the same time, GM-CSF reduced the contents of CD197+ macrophages, as well as CD14+, CD16+, and CD119+ cells among the activated cell population, without significantly altering the number of CD124+ cells. It was also shown that GM-CSF (10 ng/ml), was able to enhance production of TNFα and IL-6, but not IL-1β and IL-10 by activated Mc/Mphs. The results obtained indicate the ability of GM-CSF to exert both anti-inflammatory and pro-inflammatory effects upon macrophage cell populations. In general, such effects could contribute to the development of adaptive immunogenesis in peripheral tissues.N. D. GazatovaM. E. MeniailoV. V. MalashchenkoA. G. GoncharovO. B. MelashchenkoE. M. MorozovaV. I. SeledtsovSPb RAACIarticlegranulocyte-macrophage colony-stimulating factormonocyte/macrophagesсd-expressioncytokinesImmunologic diseases. AllergyRC581-607RUMedicinskaâ Immunologiâ, Vol 21, Iss 3, Pp 419-426 (2019) |
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DOAJ |
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RU |
topic |
granulocyte-macrophage colony-stimulating factor monocyte/macrophages сd-expression cytokines Immunologic diseases. Allergy RC581-607 |
spellingShingle |
granulocyte-macrophage colony-stimulating factor monocyte/macrophages сd-expression cytokines Immunologic diseases. Allergy RC581-607 N. D. Gazatova M. E. Meniailo V. V. Malashchenko A. G. Goncharov O. B. Melashchenko E. M. Morozova V. I. Seledtsov DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
description |
We investigated direct effects of granulocyte-macrophage colony-stimulating factor (GM-CSF) on the surface properties and cytokine-producing activity of human monocytes/macrophages (Mc/Mphs). The CD14+ cells were isolated from peripheral blood of healthy donors by positive magnetic separation. The isolated Mc/Mphs were cultured with lipopolysaccharide (LPS, 1 μg/ml) or without LPS for 24 hours. Membrane expression of CD14, CD16, CD119, CD124, and CD197 molecules was assessed by flow cytometry. The contents of tumor necrosis factor-α (TNFα), interleukin-1β (IL-1β), IL-6 and IL-10 in culture supernatants were determined by the enzyme immunoassay technique. It was found that GM-CSF at a concentration range of 0.01-10 ng/ml did significantly reduce the number of cells expressing CD197 (CC receptor of chemokine 7), without significantly affecting the percentage of CD14+ (coreceptor of LPS), CD16+ (low-affinity Fc receptor), CD119+ (IFNγ receptor) and CD124+ (IL-4 receptor) cells. At the same time, GM-CSF reduced the contents of CD197+ macrophages, as well as CD14+, CD16+, and CD119+ cells among the activated cell population, without significantly altering the number of CD124+ cells. It was also shown that GM-CSF (10 ng/ml), was able to enhance production of TNFα and IL-6, but not IL-1β and IL-10 by activated Mc/Mphs. The results obtained indicate the ability of GM-CSF to exert both anti-inflammatory and pro-inflammatory effects upon macrophage cell populations. In general, such effects could contribute to the development of adaptive immunogenesis in peripheral tissues. |
format |
article |
author |
N. D. Gazatova M. E. Meniailo V. V. Malashchenko A. G. Goncharov O. B. Melashchenko E. M. Morozova V. I. Seledtsov |
author_facet |
N. D. Gazatova M. E. Meniailo V. V. Malashchenko A. G. Goncharov O. B. Melashchenko E. M. Morozova V. I. Seledtsov |
author_sort |
N. D. Gazatova |
title |
DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
title_short |
DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
title_full |
DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
title_fullStr |
DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
title_full_unstemmed |
DIRECT EFFECTS OF GM-CSF ON THE FUNCTIONS OF HUMAN MONOCYTES/MACROPHAGES |
title_sort |
direct effects of gm-csf on the functions of human monocytes/macrophages |
publisher |
SPb RAACI |
publishDate |
2019 |
url |
https://doaj.org/article/46a92220f2b642c68919e3a8ea2bf144 |
work_keys_str_mv |
AT ndgazatova directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT memeniailo directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT vvmalashchenko directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT aggoncharov directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT obmelashchenko directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT emmorozova directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages AT viseledtsov directeffectsofgmcsfonthefunctionsofhumanmonocytesmacrophages |
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