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Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.

BACKGROUND: Human and rodent leukocytes express high levels of the glucocorticoid-inducible protein annexin 1 (ANXA1) (previously referred to as lipocortin 1). Neutrophils and monocytes have abundant ANXA1 levels. AIM: We have investigated, for the first time, ANXA1 ultrastructural expression in rat...

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Autores principales: Oliani, Sonia M, Damazo, Amilcar S, Perretti, Mauro
Formato: Texto
Lenguaje:English
Publicado: 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781677/
https://www.ncbi.nlm.nih.gov/pubmed/12467520
http://dx.doi.org/10.1080/09629350210000015683
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author Oliani, Sonia M
Damazo, Amilcar S
Perretti, Mauro
author_facet Oliani, Sonia M
Damazo, Amilcar S
Perretti, Mauro
author_sort Oliani, Sonia M
collection PubMed
description BACKGROUND: Human and rodent leukocytes express high levels of the glucocorticoid-inducible protein annexin 1 (ANXA1) (previously referred to as lipocortin 1). Neutrophils and monocytes have abundant ANXA1 levels. AIM: We have investigated, for the first time, ANXA1 ultrastructural expression in rat eosinophils and compared it with that of extravasated neutrophils. The effect of inflammation (carrageenin peritonitis) was also monitored. METHODS: Electron microscopy was used to define the sub-cellular localisation of ANXA1 in rat eosinophils and neutrophils extravasated in the mesenteric tissue. A pair of antibodies raised against the ANXA1 N-terminus (i.e. able to recognise intact ANXA1, termed LCPS1) or the whole protein (termed LCS3) was used to perform the ultrastructural analysis. RESULTS: The majority of ANXA1 was localised in the eosinophil cytosol (approximately 60%) and nucleus (30-40%), whereas a small percentage was found on the plasma membrane (< 10%). Within the cytosol, the protein was equally distributed in the matrix and in the granules, including those containing the typical crystalloid. The two anti-ANXA1 antibodies gave similar results, with the exception that LCPS1 gave a lower degree of immunoreactivity in the plasma membrane. Inflammation (i.e. carrageenin injection) produced a modest increase in eosinophil-associated ANXA1 reactivity (significant only in the cytoplasm compartment). Extravasated neutrophils, used for comparative purposes, displayed a much higher degree of immunoreactivity for the protein. CONCLUSION: We describe for the first time ANXA1 distribution in rat eosinophil by ultrastructural analysis, and report a different protein mobilisation from extravasated neutrophils, at least in this acute model of peritonitis.
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spelling pubmed-17816772007-01-25 Annexin 1 localisation in tissue eosinophils as detected by electron microscopy. Oliani, Sonia M Damazo, Amilcar S Perretti, Mauro Mediators Inflamm Research Article BACKGROUND: Human and rodent leukocytes express high levels of the glucocorticoid-inducible protein annexin 1 (ANXA1) (previously referred to as lipocortin 1). Neutrophils and monocytes have abundant ANXA1 levels. AIM: We have investigated, for the first time, ANXA1 ultrastructural expression in rat eosinophils and compared it with that of extravasated neutrophils. The effect of inflammation (carrageenin peritonitis) was also monitored. METHODS: Electron microscopy was used to define the sub-cellular localisation of ANXA1 in rat eosinophils and neutrophils extravasated in the mesenteric tissue. A pair of antibodies raised against the ANXA1 N-terminus (i.e. able to recognise intact ANXA1, termed LCPS1) or the whole protein (termed LCS3) was used to perform the ultrastructural analysis. RESULTS: The majority of ANXA1 was localised in the eosinophil cytosol (approximately 60%) and nucleus (30-40%), whereas a small percentage was found on the plasma membrane (< 10%). Within the cytosol, the protein was equally distributed in the matrix and in the granules, including those containing the typical crystalloid. The two anti-ANXA1 antibodies gave similar results, with the exception that LCPS1 gave a lower degree of immunoreactivity in the plasma membrane. Inflammation (i.e. carrageenin injection) produced a modest increase in eosinophil-associated ANXA1 reactivity (significant only in the cytoplasm compartment). Extravasated neutrophils, used for comparative purposes, displayed a much higher degree of immunoreactivity for the protein. CONCLUSION: We describe for the first time ANXA1 distribution in rat eosinophil by ultrastructural analysis, and report a different protein mobilisation from extravasated neutrophils, at least in this acute model of peritonitis. 2002-10 /pmc/articles/PMC1781677/ /pubmed/12467520 http://dx.doi.org/10.1080/09629350210000015683 Text en
spellingShingle Research Article
Oliani, Sonia M
Damazo, Amilcar S
Perretti, Mauro
Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title_full Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title_fullStr Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title_full_unstemmed Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title_short Annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
title_sort annexin 1 localisation in tissue eosinophils as detected by electron microscopy.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781677/
https://www.ncbi.nlm.nih.gov/pubmed/12467520
http://dx.doi.org/10.1080/09629350210000015683
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