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CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung

CD57 (synonyms: Leu-7, HNK-1) is a well-known marker of nerve elements including the conductive system of the heart, as well as natural killer cells. In lung specimens from 12 human fetuses at 10–34 weeks of gestation, we have found incidentally that segmental, subsegmental, and more peripheral arte...

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Autores principales: Ishizuka, Satoshi, Jin, Zhe Wu, Yamamoto, Masahito, Murakami, Gen, Takayama, Takeshi, Hayashi, Katsuhiko, Abe, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Anatomists 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026825/
https://www.ncbi.nlm.nih.gov/pubmed/29984055
http://dx.doi.org/10.5115/acb.2018.51.2.105
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author Ishizuka, Satoshi
Jin, Zhe Wu
Yamamoto, Masahito
Murakami, Gen
Takayama, Takeshi
Hayashi, Katsuhiko
Abe, Shin-ichi
author_facet Ishizuka, Satoshi
Jin, Zhe Wu
Yamamoto, Masahito
Murakami, Gen
Takayama, Takeshi
Hayashi, Katsuhiko
Abe, Shin-ichi
author_sort Ishizuka, Satoshi
collection PubMed
description CD57 (synonyms: Leu-7, HNK-1) is a well-known marker of nerve elements including the conductive system of the heart, as well as natural killer cells. In lung specimens from 12 human fetuses at 10–34 weeks of gestation, we have found incidentally that segmental, subsegmental, and more peripheral arteries strongly expressed CD57. Capillaries near developing alveoli were often or sometimes positive. The CD57-positive tissue elements within intrapulmonary arteries seemed to be the endothelium, internal elastic lamina, and smooth muscle layer, which corresponded to tissue positive for a DAKO antibody reactive with smooth muscle actin we used. However, the lobar artery and pulmonary arterial trunk as well as bronchial arteries were negative. Likewise, arteries in and along any abdominal viscera, as well as the heart, thymus, and thyroid, did not express CD57. Thus, the lung-specific CD57 reactivity was not connected with either of an endodermal- or a branchial arch-origin. CD57 antigen is a sugar chain characterized by a sulfated glucuronic acid residue that is likely to exist in some glycosphingolipids. Therefore, a chemical affinity or an interaction might exist between CD57-positive arterioles and glycosphingolipids originating from alveoli, resulting in acceleration of capillary budding to make contact with the alveolar wall. CD57 might therefore be a functional marker of the developing air-blood interface that characterizes the fetal lung at the canalicular stage.
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spelling pubmed-60268252018-07-07 CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung Ishizuka, Satoshi Jin, Zhe Wu Yamamoto, Masahito Murakami, Gen Takayama, Takeshi Hayashi, Katsuhiko Abe, Shin-ichi Anat Cell Biol Original Article CD57 (synonyms: Leu-7, HNK-1) is a well-known marker of nerve elements including the conductive system of the heart, as well as natural killer cells. In lung specimens from 12 human fetuses at 10–34 weeks of gestation, we have found incidentally that segmental, subsegmental, and more peripheral arteries strongly expressed CD57. Capillaries near developing alveoli were often or sometimes positive. The CD57-positive tissue elements within intrapulmonary arteries seemed to be the endothelium, internal elastic lamina, and smooth muscle layer, which corresponded to tissue positive for a DAKO antibody reactive with smooth muscle actin we used. However, the lobar artery and pulmonary arterial trunk as well as bronchial arteries were negative. Likewise, arteries in and along any abdominal viscera, as well as the heart, thymus, and thyroid, did not express CD57. Thus, the lung-specific CD57 reactivity was not connected with either of an endodermal- or a branchial arch-origin. CD57 antigen is a sugar chain characterized by a sulfated glucuronic acid residue that is likely to exist in some glycosphingolipids. Therefore, a chemical affinity or an interaction might exist between CD57-positive arterioles and glycosphingolipids originating from alveoli, resulting in acceleration of capillary budding to make contact with the alveolar wall. CD57 might therefore be a functional marker of the developing air-blood interface that characterizes the fetal lung at the canalicular stage. Korean Association of Anatomists 2018-06 2018-06-27 /pmc/articles/PMC6026825/ /pubmed/29984055 http://dx.doi.org/10.5115/acb.2018.51.2.105 Text en Copyright © 2018. Anatomy & Cell Biology http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ishizuka, Satoshi
Jin, Zhe Wu
Yamamoto, Masahito
Murakami, Gen
Takayama, Takeshi
Hayashi, Katsuhiko
Abe, Shin-ichi
CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title_full CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title_fullStr CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title_full_unstemmed CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title_short CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung
title_sort cd57 (leu-7, hnk-1) immunoreactivity seen in thin arteries in the human fetal lung
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6026825/
https://www.ncbi.nlm.nih.gov/pubmed/29984055
http://dx.doi.org/10.5115/acb.2018.51.2.105
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