Faculty Opinions recommendation of Activated Leukocyte Cell Adhesion Molecule Stimulates the T-Cell Response in Allergic Asthma.

Author(s):  
Mathur Kannan
2018 ◽  
Vol 197 (8) ◽  
pp. 994-1008 ◽  
Author(s):  
Mi Na Kim ◽  
Jung Yeon Hong ◽  
Doo Hee Shim ◽  
In Suk Sol ◽  
Yun Seon Kim ◽  
...  

1996 ◽  
Vol 271 (16) ◽  
pp. 9403-9409 ◽  
Author(s):  
Françoise Pagès ◽  
Marguerite Ragueneau ◽  
Sandrine Klasen ◽  
Michela Battifora ◽  
Dominique Couez ◽  
...  

Blood ◽  
1997 ◽  
Vol 89 (7) ◽  
pp. 2461-2471 ◽  
Author(s):  
Daniel R. Salomon ◽  
Laura Crisa ◽  
Christopher F. Mojcik ◽  
Jennifer K. Ishii ◽  
George Klier ◽  
...  

Abstract T-cell development requires a series of discrete selection and activation signals delivered to maturing progenitors in the thymic cortex and medulla. We have previously shown the constitutive activity of the integrin, α4β1 (VLA4), on a unique subpopulation of immature cortical thymocytes and proposed a role for integrin-mediated adhesion in positive selection by cortical epithelium. In the present report we show that thymic epithelial cell lines express vascular cell adhesion molecule-1 (VCAM-1) a high-affinity ligand for α4β1, and that VCAM-1 mediates thymocyte binding to these lines. Immunohistochemistry and confocal microscopy show that VCAM-1 is selectively expressed in situ by thymic epithelium in the cortex and corticomedullary junction, two locations at which VCAM-1 could determine the interaction between immature thymocytes and selecting elements on epithelial cells. In parallel, we confirmed that fibronectin (FN), the alternative ligand for α4β1, is expressed predominantly in the medulla. These results suggest that VCAM-1 is an adhesive ligand in the thymic cortex for the activated form of α4β1 constitutively expressed during development by immature double positive thymocytes. The structural segregation of the alternative ligand, FN, to the medulla suggests that medullary FN may regulate the migration, development, and export of more mature thymocytes.


2020 ◽  
Vol 11 ◽  
Author(s):  
Alessandro Di Gangi ◽  
Maria Elisa Di Cicco ◽  
Pasquale Comberiati ◽  
Diego G. Peroni

2018 ◽  
Vol 192 (2) ◽  
pp. 151-164 ◽  
Author(s):  
Y. S. Kim ◽  
M. N. Kim ◽  
K. E. Lee ◽  
J. Y. Hong ◽  
M. S. Oh ◽  
...  

Blood ◽  
1993 ◽  
Vol 82 (5) ◽  
pp. 1590-1598 ◽  
Author(s):  
T Ishikawa ◽  
A Imura ◽  
K Tanaka ◽  
H Shirane ◽  
M Okuma ◽  
...  

Abstract We studied the adhesion properties of peripheral blood leukemic cells from 10 patients with adult T-cell leukemia (ATL) to endothelial cells to better understand the mechanism of leukemic cell infiltration. ATL cells expressed lymphocyte function-associated antigen-1 (LFA-1), but the expression of very late antigen-4 (VLA-4) and sialyl-Lewisx (SLex) was variable. They did not express sialyl-Lewisa (SLea). Cell adhesion assays, which were performed in nine patients, showed marked adhesion of ATL cells to interleukin [IL]-1-activated human umbilical vein endothelial cells (HUVEC). A monoclonal antibody (MoAb) against E- selectin consistently inhibited ATL cell adhesion, and an MoAb against vascular cell adhesion molecule-1 (VCAM-1) or an MoAb against VLA-4 sometimes diminished it. In contrast, an MoAb against LFA-1 had a minor effect on freshly isolated ATL cell adhesion to HUVEC. The percentage of SLex+ cells in the cell population adherent to IL-1-activated HUVEC was slightly higher than that in unseparated cells. These results, together with the detection of E-selectin expression on the endothelium at ATL skin lesions, indicate that E-selectin-mediated adhesion is the major pathway for the adherence of ATL cells to endothelial cells. In addition, the ligand for E-selectin on ATL cells appears to differ from that on neutrophils.


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