Er the permeability measurements are taken. 24 hours later, fluorescently-labeled dextran was again introduced to measure the permeability after tumor cell ?endothelial cell interactions. The initial permeability value was (3.7060.59)?1026 cm/s and the tumor seeding increased endothelial permeability to (14.262.6)?1026 cm/s (p,0.05) whereas there was no significant change in the control ((6.061.1)?1026 to (6.461.9)?1026 cm/s) over the same 24 hour period. As a control, we measured the 1655472 change in endothelial permeability and extravasation rates of a normal Sudan I biological activity epithelial cell line, MCF-10A, in our microfluidic system. While extravasation was observed for 38.867.9 of the tumor cells in contact with the endothelium 1 day after seeding, the corresponding rate of MCF10A extravasation across the endothelium was lower, 23.864.7 , although not significantly different. Addition of MCF-10A also induced a 2-fold increase in permeability of endothelium from (5.7860.47)?1026 to (11.8862.15)?1026 cm/s (p,0.05) as shown in Fig. S2. This increase is smaller than the permeability increase obtained after the addition of MDA-MB-231 (3.8-fold). Therefore, the MDA-MB-231 cells show an increased tendency to extravasate and compromise endothelial barrier function compared with normal epithelial cells. These results show that our microfluidic system is capable of detecting differences among different epithelial cells lines and our results are consistent with extravasation studies in a transwell assay [41]. The change in permeability of endothelium is regulated by VEcadherin expression through the Src pathway, and the studies of in vivo models have shown that A 196 site disruption of endothelial barrier function enhanced extravasation efficiency [42]. Several mechanisms exist which could explain changes in permeability due to tumor cell interactions; the permeability increase may also be due to tumor cells locally disrupting endothelial monolayer by contact [43,44,45] or through secretion of chemical factors which then compromises the endothelial barrier function [46], but more investigation is needed for clear identification of the cause of the permeability increases.however, that the percentages of ROIs containing extravasated cells event did not show a significant change for day 1 and day 3 (72 of ROIs exhibited at least 1 extravasated cancer cell by day 1 after introducing tumor cells, and 79 of ROIs included extravasation event by day 3) (Fig. 5c), and assuming the proliferation rates are similar to both populations, this suggests most extravasation events occur within the first day the tumor cells are introduced. This observation is similar in terms of time scale for extravasation seen in vivo [17,47].ConclusionsTumor cells that disseminate from the primary tumor and intravasate into the circulatory system are transported throughout the body. By adhesion to the endothelial wall or plugging in a small capillary, the cells that survive can transmigrate across the endothelial barrier, thus providing a potential nucleating site for metastasis. Our microfluidic platform was applied to study the extravasation of a breast cancer cell line (MDA-MB-231) and their subsequent proliferation in collagen gel, which mimics the 3D nature of the extracellular space. Although microfluidics has limitations in replicating true in vivo condition, the system presented here enables a tightly-regulated and well-visualized study of cancer cell extravasation. Using this assay, we have cultured.Er the permeability measurements are taken. 24 hours later, fluorescently-labeled dextran was again introduced to measure the permeability after tumor cell ?endothelial cell interactions. The initial permeability value was (3.7060.59)?1026 cm/s and the tumor seeding increased endothelial permeability to (14.262.6)?1026 cm/s (p,0.05) whereas there was no significant change in the control ((6.061.1)?1026 to (6.461.9)?1026 cm/s) over the same 24 hour period. As a control, we measured the 1655472 change in endothelial permeability and extravasation rates of a normal epithelial cell line, MCF-10A, in our microfluidic system. While extravasation was observed for 38.867.9 of the tumor cells in contact with the endothelium 1 day after seeding, the corresponding rate of MCF10A extravasation across the endothelium was lower, 23.864.7 , although not significantly different. Addition of MCF-10A also induced a 2-fold increase in permeability of endothelium from (5.7860.47)?1026 to (11.8862.15)?1026 cm/s (p,0.05) as shown in Fig. S2. This increase is smaller than the permeability increase obtained after the addition of MDA-MB-231 (3.8-fold). Therefore, the MDA-MB-231 cells show an increased tendency to extravasate and compromise endothelial barrier function compared with normal epithelial cells. These results show that our microfluidic system is capable of detecting differences among different epithelial cells lines and our results are consistent with extravasation studies in a transwell assay [41]. The change in permeability of endothelium is regulated by VEcadherin expression through the Src pathway, and the studies of in vivo models have shown that disruption of endothelial barrier function enhanced extravasation efficiency [42]. Several mechanisms exist which could explain changes in permeability due to tumor cell interactions; the permeability increase may also be due to tumor cells locally disrupting endothelial monolayer by contact [43,44,45] or through secretion of chemical factors which then compromises the endothelial barrier function [46], but more investigation is needed for clear identification of the cause of the permeability increases.however, that the percentages of ROIs containing extravasated cells event did not show a significant change for day 1 and day 3 (72 of ROIs exhibited at least 1 extravasated cancer cell by day 1 after introducing tumor cells, and 79 of ROIs included extravasation event by day 3) (Fig. 5c), and assuming the proliferation rates are similar to both populations, this suggests most extravasation events occur within the first day the tumor cells are introduced. This observation is similar in terms of time scale for extravasation seen in vivo [17,47].ConclusionsTumor cells that disseminate from the primary tumor and intravasate into the circulatory system are transported throughout the body. By adhesion to the endothelial wall or plugging in a small capillary, the cells that survive can transmigrate across the endothelial barrier, thus providing a potential nucleating site for metastasis. Our microfluidic platform was applied to study the extravasation of a breast cancer cell line (MDA-MB-231) and their subsequent proliferation in collagen gel, which mimics the 3D nature of the extracellular space. Although microfluidics has limitations in replicating true in vivo condition, the system presented here enables a tightly-regulated and well-visualized study of cancer cell extravasation. Using this assay, we have cultured.
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