<p>HUVEC and bEND3 cells were plated on 60 mm plates and allowed to grow to 80% confluency. The semi-confluent cell layer was scraped using a 200 µl sterile pipette tip to create a scratch/wound devoid of cells. The remaining cells were treated with vehicle control or 300 nM PLA-695 for 45 min prior to IR with 3 Gy. Migration was assessed at 24 h after treatment. The number of cells migrated in the scratch/wound were counted and normalized to surrounding cell density per HPF. Shown are representative photomicrographs and bar graphs representing the mean percentages of migrating cells relative to corresponding controls with SEM from three experiments.</p
BACKGROUND: To overcome the compromised wound healing in radiation induced chronic wounds platelet-...
<p>SHSY5Y cells were cultured in the presence or absence of 10 mM ManNAc, ManNProp or ManNPent. Cell...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
<p>Equal numbers of bEND3, HUVEC, LLC and A549 cells were plated in 96 well plates and treated with ...
Cell migration affects many physiologic and pathologic processes in mammalian organisms. Thus, our a...
<p>Cell suspensions were obtained 24 hours after irradiation at a total dose of 4 Gy, and then they ...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>HUVEC migration was detected using a scratch wound assay. The cell monolayer was scraped with a s...
<p>A: HMEC-1 cells were seeded in the same density as for the proliferation assay and treated with t...
<p>Confluent cell cultures were wounded post-treatment and migration distances were measured at 8 ho...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>The transwell assay was performed by using a 24-well chamber as the outer chambers and polycarbon...
<p>The normal untreated and irradiated veins were separately cultured on fibronectin-coated culture ...
<p>Raw264.7 cells given 2Gy or 0Gy radiation were placed in the upper chamber with no FBS, and mediu...
<p>Inhibition of vascular tube formation of HUVEC endothelial cells (A) and inhibition of migration ...
BACKGROUND: To overcome the compromised wound healing in radiation induced chronic wounds platelet-...
<p>SHSY5Y cells were cultured in the presence or absence of 10 mM ManNAc, ManNProp or ManNPent. Cell...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...
<p>Equal numbers of bEND3, HUVEC, LLC and A549 cells were plated in 96 well plates and treated with ...
Cell migration affects many physiologic and pathologic processes in mammalian organisms. Thus, our a...
<p>Cell suspensions were obtained 24 hours after irradiation at a total dose of 4 Gy, and then they ...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>HUVEC migration was detected using a scratch wound assay. The cell monolayer was scraped with a s...
<p>A: HMEC-1 cells were seeded in the same density as for the proliferation assay and treated with t...
<p>Confluent cell cultures were wounded post-treatment and migration distances were measured at 8 ho...
<p>(A and B) To measure cell migration activity, A549 (left panels) and Panc-1 (right panels) cells ...
<p>The transwell assay was performed by using a 24-well chamber as the outer chambers and polycarbon...
<p>The normal untreated and irradiated veins were separately cultured on fibronectin-coated culture ...
<p>Raw264.7 cells given 2Gy or 0Gy radiation were placed in the upper chamber with no FBS, and mediu...
<p>Inhibition of vascular tube formation of HUVEC endothelial cells (A) and inhibition of migration ...
BACKGROUND: To overcome the compromised wound healing in radiation induced chronic wounds platelet-...
<p>SHSY5Y cells were cultured in the presence or absence of 10 mM ManNAc, ManNProp or ManNPent. Cell...
BACKGROUND: Cell migration is a vital process for growth and repair. In vitro migration assays, util...