Figure 3 - HCELL+ MSCs have markedly enhanced shear-resistant adhesive interactions with endothelial E-selectin under defined shear stress conditions.


From the following article

Ex vivo glycan engineering of CD44 programs human multipotent mesenchymal stromal cell trafficking to bone

Robert Sackstein, Jasmeen S Merzaban, Derek W Cain, Nilesh M Dagia, Joel A Spencer, Charles P Lin & Roland Wohlgemuth

Nature Medicine 14, 181 - 187 (2008) Published online: 13 January 2008

doi:10.1038/nm1703

BACK TO ARTICLE
Unfortunately we are unable to provide accessible alternative text for this. If you require assistance to access this image, or to obtain a text description, please contact npg@nature.com

Untreated MSCs, HCELL+ MSCs or sialidase-digested FTVI-treated (FTVI-sialidase-MSCs) MSCs were perfused over IL-1beta and TNF-alpha stimulated (stim) or unstimulated (unstim) HUVECs at 0.5 dyn/cm2. MSC accumulation was then determined at shear stresses of 0.5, 1, 2, 5, 10, 20 and 30 dyn/cm2. HCELL+ MSCs show rolling adhesive interactions on HUVECs at a shear stress of up to 30 dyn/cm2 that were abrogated by sialidase treatment. To control for the specificity of binding of HCELL+ MSCs, EDTA was added to the assay buffer (EDTA group), or stimulated HUVECs were pretreated with a function blocking mAb to E-selectin (anti–E-Sel group) before use in adhesion assays. Values are means plusminus s.e.m. (n = 4 for each group). P < 0.001 for comparisons of HCELL+ MSCs to all other groups at all shear stress levels.

BACK TO ARTICLE