Developmental Changes of Cell Adhesion Molecule Expression in the Fetal Mouse Liver

2010 ◽  
Vol 293 (10) ◽  
pp. 1698-1710 ◽  
Author(s):  
Yoshinori Sugiyama ◽  
Toru Koike ◽  
Nobuyoshi Shiojiri
Keyword(s):  
Cell Adhesion ◽  
Adhesion Molecule ◽  
Mouse Liver ◽  
Cell Adhesion Molecule ◽  
Developmental Changes ◽  
Adhesion Molecule Expression ◽  
Fetal Mouse ◽  
Fetal Mouse Liver

Tanycyte morphology and cell adhesion molecule expression are regulated by photoperiod

2010 ◽  
Vol 41 (01) ◽  
Author(s):  
S Steinlechner ◽  
M Bolborea ◽  
P Pévet ◽  
P Klosen
Keyword(s):  
Cell Adhesion ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Adhesion Molecule Expression

scholarly journals Platelet and Endothelial Cell Adhesion Molecule Expression in Pregnant Women with Preeclampsia

2019 ◽  
Vol 15 (3) ◽  
pp. 193-197
Author(s):  
Murat Alan ◽  
Beril Gürlek ◽  
Alpay Yılmaz ◽  
Neşe Lortlar ◽  
Ahmet Nuri Danışman
Keyword(s):  
Cell Adhesion ◽  
Endothelial Cell ◽  
Pregnant Women ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Adhesion Molecule Expression ◽  
Endothelial Cell Adhesion Molecule ◽  
Endothelial Cell Adhesion

Endothelial cell adhesion molecule expression in interleukin-10 deficient mice

1998 ◽  
Vol 114 ◽  
pp. A400
Author(s):  
Z Morise ◽  
E Conner ◽  
M Eppihimer ◽  
DN Granger ◽  
DC Anderson ◽  
...  
Keyword(s):  
Cell Adhesion ◽  
Endothelial Cell ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Interleukin 10 ◽  
Adhesion Molecule Expression ◽  
Endothelial Cell Adhesion Molecule ◽  
Deficient Mice ◽  
Endothelial Cell Adhesion

Abstract 527: The Functional Significance of the Adenosine A 2b Receptor in the Internal Mammary Artery

2017 ◽  
Vol 37 (suppl_1) ◽  
Author(s):  
Stephen R Archacki ◽  
Qing K Wang
Keyword(s):  
Cell Adhesion ◽  
Coronary Arteries ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Transendothelial Migration ◽  
Adhesion Molecule Expression ◽  
Monocyte Adhesion ◽  
Knowing That ◽  
Mammary Arteries ◽  
Internal Mammary

Objective: The endothelium is the initial target that leads to cardiovascular disease. Knowing that the internal mammary arteries (IMA) are resistant to the development of atherosclerosis, which contrasts with coronary arteries (Cor) which are athero-prone, we hypothesize that genes over-expressed in the endothelial cells (ECs) of between these two arteries will identify genes that resist atherosclerosis. Methods and Results: Microarray analysis showed over 1,000 differentially expressed in the ECs of IMA vs Cor. The most statistically significant different gene was the adenosine A 2B receptor. This indicates the A 2B receptor may be involved in a resistance to atherosclerosis. Western blot analysis showed higher A 2B expression in the IMA than in coronary arteries with or without disease from proteins harvested from these human arteries and ECs. Overexpression of A 2B in ECs blunted: monocyte adhesion, cell adhesion molecule expression, migration, and the transendothelial migration of monocytes-- processes directly associated with the development of atherosclerosis. Knockdown of A 2B expression by siRNA promoted these processes. Conclusions: ECs derived from the IMA and Cor are distinctly different in gene expression, which may be responsible for their differential sensitivities for atherosclerosis. This study defined how the A 2B receptor may act as an atherosclerotic-resistance gene, which blunted monocyte adhesion and cell adhesion molecule expression, EC migration and retarded the transendothelial migration of monocytes.

Neural cell adhesion molecule expression in thyroid cancer

1996 ◽  
Author(s):  
Y Miyajima ◽  
S Ota ◽  
H Yasukawa ◽  
M Zenmyou ◽  
M Morimatsu ◽  
...  
Keyword(s):  
Thyroid Cancer ◽  
Cell Adhesion ◽  
Adhesion Molecule ◽  
Cell Adhesion Molecule ◽  
Neural Cell Adhesion Molecule ◽  
Neural Cell ◽  
Adhesion Molecule Expression ◽  
Neural Cell Adhesion
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