Corrigendum to “The biosynthesis of the selectin-ligand sialyl Lewis x in colorectal cancer tissues is regulated by fucosyltransferase VI and can be inhibited by an RNA interference-based approach” [Int. J. Biochem. Cell Biol. 43 (1) (2011) 130–139]

2011 ◽  
Vol 43 (11) ◽  
pp. 1649-1650
Author(s):  
Marco Trinchera ◽  
Nadia Malagolini ◽  
Mariella Chiricolo ◽  
Donatella Santini ◽  
Francesco Minni ◽  
...  
Keyword(s):  
Colorectal Cancer ◽  
Rna Interference ◽  
Sialyl Lewis X ◽  
Lewis X ◽  
Sialyl Lewis ◽  
Cell Biol ◽  
Selectin Ligand ◽  
Cancer Tissues

Sulfated Sialyl Lewis X, the Putative L-Selectin Ligand, Detected on Endothelial Cells of High Endothelial Venules by a Distinct Set of Anti-Sialyl Lewis X Antibodies

1997 ◽  
Vol 230 (3) ◽  
pp. 546-551 ◽  
Author(s):  
Chikako Mitsuoka ◽  
Naoko Kawakami-Kimura ◽  
Mikiko Kasugai-Sawada ◽  
Nozomu Hiraiwa ◽  
Ken'ichi Toda ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Sialyl Lewis X ◽  
Lewis X ◽  
High Endothelial Venules ◽  
Sialyl Lewis ◽  
Selectin Ligand

scholarly journals Identification of a Major Carbohydrate Capping Group of the L-selectin Ligand on High Endothelial Venules in Human Lymph Nodes as 6-Sulfo Sialyl Lewis X

1998 ◽  
Vol 273 (18) ◽  
pp. 11225-11233 ◽  
Author(s):  
Chikako Mitsuoka ◽  
Mikiko Sawada-Kasugai ◽  
Keiko Ando-Furui ◽  
Mineko Izawa ◽  
Hayao Nakanishi ◽  
...  
Keyword(s):  
Lymph Nodes ◽  
Sialyl Lewis X ◽  
Lewis X ◽  
High Endothelial Venules ◽  
Sialyl Lewis ◽  
Selectin Ligand

scholarly journals Human Synovial Lubricin Expresses Sialyl Lewis x Determinant and Has L-selectin Ligand Activity

2012 ◽  
Vol 287 (43) ◽  
pp. 35922-35933 ◽  
Author(s):  
Chunsheng Jin ◽  
Anna-Karin Hultgård Ekwall ◽  
Johan Bylund ◽  
Lena Björkman ◽  
Ruby P. Estrella ◽  
...  
Keyword(s):  
Sialyl Lewis X ◽  
Lewis X ◽  
Sialyl Lewis ◽  
Selectin Ligand ◽  
Ligand Activity

Syntheses of 6-Sulfo Sialyl Lewis X Glycans Corresponding to thel-Selectin Ligand “Sulfoadhesin”

2004 ◽  
Vol 6 (14) ◽  
pp. 2345-2348 ◽  
Author(s):  
Matthew R. Pratt ◽  
Carolyn R. Bertozzi
Keyword(s):  
Sialyl Lewis X ◽  
Lewis X ◽  
Sialyl Lewis ◽  
Selectin Ligand

scholarly journals Evaluation of Strategies Aimed at Improving Liver Progenitor Cell Rolling and Subsequent Adhesion to the Endothelium

2020 ◽  
Vol 29 ◽  
pp. 096368972091270
Author(s):  
Pierre Edouard Dollet ◽  
Mei Ju Hsu ◽  
Jérôme Ambroise ◽  
Milena Rozzi ◽  
Joachim Ravau ◽  
...  
Keyword(s):  
Endothelial Cells ◽  
Cell Adhesion ◽  
Alternative Methods ◽  
Sialyl Lewis X ◽  
Thermosensitive Polymer ◽  
Lewis X ◽  
Promising Alternative ◽  
Sialyl Lewis ◽  
Selectin Ligand

Adult-derived human liver stem/progenitor cells (ADHLSCs) are a promising alternative to orthotopic liver transplantation in the treatment of inborn errors of metabolism. However, as is the case with many mesenchymal stromal cells, ADHLSCs have shown a low level of engraftment, which could be explained by the fact that they lack expression of selectin ligand and LFA-1 and only slightly express VLA- 4, molecules that have been shown to be involved in cell adhesion to the endothelium. In this paper, we have investigated strategies to increase their rolling and adhesion during the homing process by (1) adding a selectin ligand (Sialyl Lewis X) to their surface using biotinyl- N-hydroxy-succinimide–streptavidin bridges, and (2) protecting the adhesion proteins from trypsinization-induced damage using a thermosensitive polymer for cell culture and a nonenzymatic cell dissociation solution (CDS) for harvest. Despite increasing adhesion of ADHLSCs to E-selectin during an adhesion test in vitro performed under shear stress, the addition of Sialyl Lewis X did not increase adhesion to endothelial cells under the same conditions. Cultivating cells on a thermosensitive polymer and harvesting them with CDS increased their adhesion to endothelial cells under noninflammatory conditions, compared to the use of trypsin. However, we were not able to demonstrate any improvement in cell adhesion to the endothelium following culture on polymer and harvest with CDS, suggesting that alternative methods of improving engraftment still need to be evaluated.

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