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. Author manuscript; available in PMC: 2014 May 21.
Published in final edited form as: Soft Matter. 2014 Mar 21;10(11):1644–1659. doi: 10.1039/c3sm51910d

Fig. 12.

Fig. 12

Schematic view of endothelial cell monolayers with adhering WBC in the resting state. The leucocyte (WBC; shown on the left side) exposes ~5000 microvilli (length 0.3–0.5 μm; width 150 nm).76 The number of PSLG-1 receptors (5 × 105) is 100 times larger than that of microvilli, suggesting that the tip is coupled to several PSLG-1–selectins bonds. The WBCs expose receptors for cytokines (abbreviated as Gαβχ) which activate the cell through the heterogenous membrane bound GTPase Gαβγ. (b) Reproduced from E. Sackmann and R. Merkel, Lehrbuch der Biophysik, Wiley Verlag, Weinheim, 2010. Penetration of the excited lymphocyte through the ENC-layer triggered by cytokines (such as interleukin-8). They bind to specific receptors on the blood cells which increases the density of high affinity integrins LFA-1 on the WBCs while the repellant glycoproteins are removed from the front. Bottom left: electron micrograph showing activated cell (granulocyte) penetrating through the endothelial cell monolayer (reproduced from ref. 77) The driving force is provided by the gain in binding energy between integrin (LFA-1) and ICAM. Bottom right: opening of a gap between ENC monolayers by the hormone histamine and thrombin.78