“…Because of the low-velocity blood flow, the sinusoids capture leukocytes or tumor cells in the absence of or with little participation from selectins [36], although the exact mechanism of cell trapping at the sinusoids remains to be fully elucidated. Recently, a 170-kDa homodimeric sialoglycoprotein, VAP-1, that is expressed constitutively in hepatic sinusoidal endothelial cells has been proposed to mediate shear-dependent adhesion in the liver, based on the observation that VAP-1 can mediate lymphocyte adhesion and transmigration under flow conditions in vitro [37]. Given that multiple adhesion molecules are generally required for any kind of cell adhesion, we speculate that not only VAP-1 but also other adhesion molecules such as CD44 are involved in shear-dependent cell adhesion in the liver.…”