CD57 (Leu-7, HNK-1) immunoreactivity seen in thin arteries in the human fetal lung.
10.5115/acb.2018.51.2.105
- Author:
Satoshi ISHIZUKA
1
;
Zhe Wu JIN
;
Masahito YAMAMOTO
;
Gen MURAKAMI
;
Takeshi TAKAYAMA
;
Katsuhiko HAYASHI
;
Shin ichi ABE
Author Information
1. Department of Anatomy, Tokyo Dental College, Tokyo, Japan. yamamotomasahito@tdc.ac.jp
- Publication Type:Original Article
- Keywords:
CD57;
Leu-7;
HNK-1;
Lung;
Human fetus
- MeSH:
Acceleration;
Actins;
Antigens, CD57;
Arteries*;
Arterioles;
Bronchial Arteries;
Capillaries;
Endothelium;
Fetus;
Glucuronic Acid;
Glycosphingolipids;
Heart;
Humans*;
Killer Cells, Natural;
Lung*;
Muscle, Smooth;
Pregnancy;
Thymus Gland;
Thyroid Gland;
Viscera
- From:Anatomy & Cell Biology
2018;51(2):105-112
- CountryRepublic of Korea
- Language:English
-
Abstract:
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.
