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CD13
This chapter focuses on the tissue distribution, structure, and functions of the leucocyte antigen CD13. CD13 is expressed by granulocytes and monocytes and their precursors. CD13 is a marker for most acute myeloid leukaemias and a smaller proportion of acute lymphoid leukaemias. Various nonhematopo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
1997
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155611/ http://dx.doi.org/10.1016/B978-012078185-0/50447-9 |
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author | Barclay, A. Neil Brown, Marion H. Law, S.K. Alex McKnight, Andrew J. Tomlinson, Michael G. van der Merwe, P. Anton |
author_facet | Barclay, A. Neil Brown, Marion H. Law, S.K. Alex McKnight, Andrew J. Tomlinson, Michael G. van der Merwe, P. Anton |
author_sort | Barclay, A. Neil |
collection | PubMed |
description | This chapter focuses on the tissue distribution, structure, and functions of the leucocyte antigen CD13. CD13 is expressed by granulocytes and monocytes and their precursors. CD13 is a marker for most acute myeloid leukaemias and a smaller proportion of acute lymphoid leukaemias. Various nonhematopoietic cells express CD13, including epithelial cells from renal proximal tubules and intestinal brush border, endothelial cells, fibroblasts, brain cells, bone marrow stromal cells, osteoclasts, and cells lining the biliary caniculae. CD13 is a member of a group of type II integral membrane metalloproteases that includes the leucocyte antigens CD10, CD26, CD73, and BP-1. The CD13 glycoprotein has a short N-terminal cytoplasmic tail, a transmembrane region that functions as a signal peptide, and a large C-terminal extracellular region that contains 11 N-linked glycosylation sites and also O-linked glycosylation. CD13 is a receptor for coronaviruses, RNA viruses that cause respiratory diseases in humans and several species of animals. The binding site on CD 13 for the swine coronavirus TGEV (transmissible gastroenteritis virus) is distinct from the enzymatic site. CD13 is a zinc-binding metalloprotease that plays a role in cell surface antigen presentation by trimming the N-terminal amino acids from MHC Class II-bound peptides. |
format | Online Article Text |
id | pubmed-7155611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1997 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71556112020-04-15 CD13 Barclay, A. Neil Brown, Marion H. Law, S.K. Alex McKnight, Andrew J. Tomlinson, Michael G. van der Merwe, P. Anton The Leucocyte Antigen FactsBook Article This chapter focuses on the tissue distribution, structure, and functions of the leucocyte antigen CD13. CD13 is expressed by granulocytes and monocytes and their precursors. CD13 is a marker for most acute myeloid leukaemias and a smaller proportion of acute lymphoid leukaemias. Various nonhematopoietic cells express CD13, including epithelial cells from renal proximal tubules and intestinal brush border, endothelial cells, fibroblasts, brain cells, bone marrow stromal cells, osteoclasts, and cells lining the biliary caniculae. CD13 is a member of a group of type II integral membrane metalloproteases that includes the leucocyte antigens CD10, CD26, CD73, and BP-1. The CD13 glycoprotein has a short N-terminal cytoplasmic tail, a transmembrane region that functions as a signal peptide, and a large C-terminal extracellular region that contains 11 N-linked glycosylation sites and also O-linked glycosylation. CD13 is a receptor for coronaviruses, RNA viruses that cause respiratory diseases in humans and several species of animals. The binding site on CD 13 for the swine coronavirus TGEV (transmissible gastroenteritis virus) is distinct from the enzymatic site. CD13 is a zinc-binding metalloprotease that plays a role in cell surface antigen presentation by trimming the N-terminal amino acids from MHC Class II-bound peptides. 1997 2007-09-02 /pmc/articles/PMC7155611/ http://dx.doi.org/10.1016/B978-012078185-0/50447-9 Text en Copyright © 1997 Elsevier 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 Barclay, A. Neil Brown, Marion H. Law, S.K. Alex McKnight, Andrew J. Tomlinson, Michael G. van der Merwe, P. Anton CD13 |
title | CD13 |
title_full | CD13 |
title_fullStr | CD13 |
title_full_unstemmed | CD13 |
title_short | CD13 |
title_sort | cd13 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155611/ http://dx.doi.org/10.1016/B978-012078185-0/50447-9 |
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