Figure 1
Figure 1. Cell surface engineered MSCs display enhanced rolling intactions in vitro. (A) Conjugation of sLex on the surface of the MSCs through covalent biotinylation and a streptavidin-biotin bridge. (B) Velocity of sLex-modified cells compared with PBS-treated cells and glucose-modified cells at 0.36 dyne/cm2 on P-selectin–coated substrates. (C) Number of interacting sLex-modified cells compared with PBS-treated cells and glucose-modified cells per unit area at 0.36 dyne/cm2 on P-selectin–coated substrate over 10 seconds with 0.45 mm2 area. (D) Velocity of sLex-modified MSCs, HL60, and free stream velocity (theoretically calculated from flow chamber geometry and fluid flow rate) at increasing shear stress.

Cell surface engineered MSCs display enhanced rolling intactions in vitro. (A) Conjugation of sLex on the surface of the MSCs through covalent biotinylation and a streptavidin-biotin bridge. (B) Velocity of sLex-modified cells compared with PBS-treated cells and glucose-modified cells at 0.36 dyne/cm2 on P-selectin–coated substrates. (C) Number of interacting sLex-modified cells compared with PBS-treated cells and glucose-modified cells per unit area at 0.36 dyne/cm2 on P-selectin–coated substrate over 10 seconds with 0.45 mm2 area. (D) Velocity of sLex-modified MSCs, HL60, and free stream velocity (theoretically calculated from flow chamber geometry and fluid flow rate) at increasing shear stress.

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