DISTRIBUTION OF THE CD15 EPITOPE IN THE MAMMALIAN DEVELOPING LUNG IS OPPOSITE IN MOUSE COMPARED WITH HUMAN

Authors
Citation
D. Nohr et Jk. Mai, DISTRIBUTION OF THE CD15 EPITOPE IN THE MAMMALIAN DEVELOPING LUNG IS OPPOSITE IN MOUSE COMPARED WITH HUMAN, Differentiation, 63(1), 1998, pp. 43-49
Citations number
36
Categorie Soggetti
Developmental Biology","Cell Biology
Journal title
ISSN journal
03014681
Volume
63
Issue
1
Year of publication
1998
Pages
43 - 49
Database
ISI
SICI code
0301-4681(1998)63:1<43:DOTCEI>2.0.ZU;2-O
Abstract
The distribution of the expression of the CD15 epitope was characteriz ed by immunohistochemistry in the developing mouse and human lung on e mbryonic days E9.5-E19 and gestational weeks GW7-GW25, respectively. I n the earliest stages in the mouse, the tracheal epithelial cells expr essed CD15 on their apical and lateral cell membranes and, in the more proximal regions, also showed a faint cytoplasmatic CD15 expression. Only very few epithelial cells in the bronchial bud regions expressed CD15 on their apical surfaces. In later stages (E12-E17), cells in the proximal parts of the bronchi and bronchioli expressed CD15 on their apical, but also on their lateral membranes, and increasing numbers of cells expressed CD15 cytoplasmatically. Cells in the distal, presumab ly proliferating, areas of the bud regions were CD15 negative. This di stribution pattern of CD15 was consistent until the latest embryonic s tages. These results are completely opposite to those found in human d eveloping lung where up to GW20 bronchial and bronchiolar bud regions were CD15 positive, while in the proximal parts of the airways the vas t majority of cells were CD15 negative. After GW20, CD15 immunoreactiv ity in the bud regions vanished and was completely absent on GW25. Thi s difference between human and mouse adds further evidence to profound species differences in the expression of CD15 in various organs, e.g. , in the cerebellum or the retina, and should be taken into account wh en considering functional roles of CD15 and also when relating results from a (transgenic) mouse model to the respective human organ system.