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Differential expression of sialic acid on porcine organs during the maturation process

Sialylated structures play important roles in cell communication, and change in a regulated manner during development and differentiation. In this work, we report the main glycosidic modifications that occur during the maturation of porcine tissues, involving the sialylation process as determined wi...

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Detalles Bibliográficos
Autores principales: Vallejo, Verónica, Reyes-Leyva, Julio, Hernández, Jesús, Ramírez, Humberto, Delannoy, Philippe, Zenteno, Edgar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science Inc. 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129425/
https://www.ncbi.nlm.nih.gov/pubmed/11007184
http://dx.doi.org/10.1016/S0305-0491(00)00213-3
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author Vallejo, Verónica
Reyes-Leyva, Julio
Hernández, Jesús
Ramírez, Humberto
Delannoy, Philippe
Zenteno, Edgar
author_facet Vallejo, Verónica
Reyes-Leyva, Julio
Hernández, Jesús
Ramírez, Humberto
Delannoy, Philippe
Zenteno, Edgar
author_sort Vallejo, Verónica
collection PubMed
description Sialylated structures play important roles in cell communication, and change in a regulated manner during development and differentiation. In this work, we report the main glycosidic modifications that occur during the maturation of porcine tissues, involving the sialylation process as determined with lectins. Sialic acids were identified at several levels in a broad range of cell types of nervous, respiratory, genitourinary and lymphoid origin. Nevertheless, the most contrasting was the type of glycosidic linkage between 5-N-acetyl-neuraminic acid (Neu5Ac) and galactose (Gal) expressed in central nervous system (CNS). Newborn CNS abundantly expressed Neu5Acα2,3Gal, but weakly or scarcely expressed Neu5Acα2,6Gal/GalNAc. Maturation of CNS induced drastic changes in sialic acid expression. These changes include decrease or complete loss of NeuAcα2,3Gal residues, mainly in olfactory structures and brain cortex, which were replaced by their isomers Neu5Acα2,6Gal/GalNAc. In the brain cortex and cerebellum, the increase of Neu5Acα2,6Gal/GalNAc molecules was paralleled by an increase of 5-N-acetyl-9-O-acetyl-neuraminic acid (Neu5,9Ac2). In addition, terminal Gal and N-acetyl-d-galactosamine (GalNAc) residues also increased their expression in adult CNS tissues, but this was more significant in structures forming the encephalic trunk. Our results show that sialylation of porcine CNS is finely modulated throughout the maturation process.
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spelling pubmed-71294252020-04-08 Differential expression of sialic acid on porcine organs during the maturation process Vallejo, Verónica Reyes-Leyva, Julio Hernández, Jesús Ramírez, Humberto Delannoy, Philippe Zenteno, Edgar Comp Biochem Physiol B Biochem Mol Biol Article Sialylated structures play important roles in cell communication, and change in a regulated manner during development and differentiation. In this work, we report the main glycosidic modifications that occur during the maturation of porcine tissues, involving the sialylation process as determined with lectins. Sialic acids were identified at several levels in a broad range of cell types of nervous, respiratory, genitourinary and lymphoid origin. Nevertheless, the most contrasting was the type of glycosidic linkage between 5-N-acetyl-neuraminic acid (Neu5Ac) and galactose (Gal) expressed in central nervous system (CNS). Newborn CNS abundantly expressed Neu5Acα2,3Gal, but weakly or scarcely expressed Neu5Acα2,6Gal/GalNAc. Maturation of CNS induced drastic changes in sialic acid expression. These changes include decrease or complete loss of NeuAcα2,3Gal residues, mainly in olfactory structures and brain cortex, which were replaced by their isomers Neu5Acα2,6Gal/GalNAc. In the brain cortex and cerebellum, the increase of Neu5Acα2,6Gal/GalNAc molecules was paralleled by an increase of 5-N-acetyl-9-O-acetyl-neuraminic acid (Neu5,9Ac2). In addition, terminal Gal and N-acetyl-d-galactosamine (GalNAc) residues also increased their expression in adult CNS tissues, but this was more significant in structures forming the encephalic trunk. Our results show that sialylation of porcine CNS is finely modulated throughout the maturation process. Elsevier Science Inc. 2000-07 2000-08-07 /pmc/articles/PMC7129425/ /pubmed/11007184 http://dx.doi.org/10.1016/S0305-0491(00)00213-3 Text en Copyright © 2000 Elsevier Science Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Vallejo, Verónica
Reyes-Leyva, Julio
Hernández, Jesús
Ramírez, Humberto
Delannoy, Philippe
Zenteno, Edgar
Differential expression of sialic acid on porcine organs during the maturation process
title Differential expression of sialic acid on porcine organs during the maturation process
title_full Differential expression of sialic acid on porcine organs during the maturation process
title_fullStr Differential expression of sialic acid on porcine organs during the maturation process
title_full_unstemmed Differential expression of sialic acid on porcine organs during the maturation process
title_short Differential expression of sialic acid on porcine organs during the maturation process
title_sort differential expression of sialic acid on porcine organs during the maturation process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129425/
https://www.ncbi.nlm.nih.gov/pubmed/11007184
http://dx.doi.org/10.1016/S0305-0491(00)00213-3
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