Figure 4.
Figure 4. Persisting migration of CD4+ blasts in the presence of protease inhibitors. Migration in 3D collagen (A-B) and multicomponent matrices (C) in the absence or presence of protease inhibitor cocktail. (A) Digitized paths of 40 cells at orthotopic position (2-hour tracking period; 1 representative of 3 independent experiments). (B-C) Steady-state velocity and percentage of migrating CD4+ T cells in collagen (B) and collagen copolymerized with hyaluronan and chondroitin sulfate (C). Data show the means of time-dependent population parameters ± SDs for 3 independent experiments (120 cells).

Persisting migration of CD4+blasts in the presence of protease inhibitors. Migration in 3D collagen (A-B) and multicomponent matrices (C) in the absence or presence of protease inhibitor cocktail. (A) Digitized paths of 40 cells at orthotopic position (2-hour tracking period; 1 representative of 3 independent experiments). (B-C) Steady-state velocity and percentage of migrating CD4+ T cells in collagen (B) and collagen copolymerized with hyaluronan and chondroitin sulfate (C). Data show the means of time-dependent population parameters ± SDs for 3 independent experiments (120 cells).

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