The mean velocity of THP-1 cell migration on matrigel coated glass appears to be slightly slower than that of mouse neutrophils migrating in EZ-Taxiscan chambers on fibrinogen coated glass, 0.08 µm/sec vs. 0.11 µm/sec, respectively [10].
Overall the velocity of migration and the MI of THP-1 cells are only moderately less efficient compared with parameters reported for primary mouse neutrophils migrating in EZ-Taxiscan chambers on fibrinogen coated glass [10].
To address this question, we monitored intracellular Ca2+ dynamics in mouse bone marrow-derived DCs migrating in fibronectin-coated 5 × 5 μm micro-fabricated channels.
High levels of H4/H2A R3me2s have also been reported in human GW 19 gonocytes (Eckert et al, 2008), matching the epigenetic profile of migrating PGCs in mice (Seki et al, 2007; Hajkova et al, 2008).
The average of the numbers within the four circles was considered the number of leukocytes migrated in the retina for each mouse.
In summary, we report here that the dioxin receptor is a novel regulator of caveolin-1 distribution and function in migrating mouse fibroblasts.
In addition, mouse peritoneal exudate cells (PECs) derived from CCR2 deficient (Ccr2−/−) C57BL/6 mice fail to migrate in response to hBD-3 (Joost Oppenheim; personal communication).
Next, we determined whether mouse FLS would migrate in response to human RA SF.
Sahota et al. found that at 1 day after the stent implanted with human microvascular endothelial cells was implanted in nude mouse, endothelial cells migrated in the stent.
Synovial fibroblasts also can migrate in the bloodstream to invade distant cartilage in mouse models [ 22], which may explain how multiple joints are involved in rheumatoid arthritis.
