<p>HaCaT cells and fibroblasts were grown in 6-well plates until the 100% confluence was reached, then cells were starved for the next 12 hours in DMEM without 10% FCS and scratched once vertically with a 200μL pipette tip. After being washed two times with sterile PBS, a fresh portion of DMEM medium was added and cells were treated with the tested peptides applied at their optimal doses (25 μg/mL). Migration was analyzed after 24 hours by means of Zeiss Observer D1 microscope, wounding areas were analyzed with AxioVision software and expressed as the percentage of the wound width in comparison to the control sample (cells incubated in DMEM without FCS). Control+ FCS corresponds to the sample with cells incubated in the medium containing 10...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>Experiments were conducted using PES43 cells. (A) Migration was assayed in 24-well Transwell cham...
<p>Wound healing of human dermal fibroblast monolayers was evaluated by an <i>in vitro</i> scratch a...
<p>Cells were incubated with 1 µg/mL TE, 10 ng/mL HGF or treated with DMSO, as control. Images were ...
<p>A—control probe for keratinocytes, B—migration of keratinocytes in the presence of the peptide (2...
<p>Scratch wounds of FB (<b>A</b>) and KC (<b>D</b>) are shown. One representative experiment of thr...
<p>(A) 800 peptide or 800SCR tagged with tetramethylrhodamine (TMR) were added to primary keratinocy...
<p>Scratch wound assay <i>in vitro</i>. (A) Representative phase-contrast images of RbTCF cells imme...
<p>A) <i>In vitro</i> migration of K5-GR and K5-GR-TR primary keratinocytes isolated from WT, K5-GR ...
<p>HaCaT cells were seeded in each side of an ibidi culture insert and grown to confluence. Afterwar...
<p>(A): two monolayers of HaCaT cells separated by a defined distance were treated with LL-37 at dif...
<p><b>A.</b> Significantly increased (*p<0.03) cell migration occurred in NF over a 30 hrs period fo...
<p>HaCaT keratinocytes were used to determine the effect of VPA on human keratinocyte migration. Cel...
<p>(A-C) HCFs were scratched and the relative cell migration percentage was quantified at 0, 4, 24, ...
<p>NIH-3T3 fibroblasts were grown to confluency on fibronectin (A&B) or collagen (C) coated coversli...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>Experiments were conducted using PES43 cells. (A) Migration was assayed in 24-well Transwell cham...
<p>Wound healing of human dermal fibroblast monolayers was evaluated by an <i>in vitro</i> scratch a...
<p>Cells were incubated with 1 µg/mL TE, 10 ng/mL HGF or treated with DMSO, as control. Images were ...
<p>A—control probe for keratinocytes, B—migration of keratinocytes in the presence of the peptide (2...
<p>Scratch wounds of FB (<b>A</b>) and KC (<b>D</b>) are shown. One representative experiment of thr...
<p>(A) 800 peptide or 800SCR tagged with tetramethylrhodamine (TMR) were added to primary keratinocy...
<p>Scratch wound assay <i>in vitro</i>. (A) Representative phase-contrast images of RbTCF cells imme...
<p>A) <i>In vitro</i> migration of K5-GR and K5-GR-TR primary keratinocytes isolated from WT, K5-GR ...
<p>HaCaT cells were seeded in each side of an ibidi culture insert and grown to confluence. Afterwar...
<p>(A): two monolayers of HaCaT cells separated by a defined distance were treated with LL-37 at dif...
<p><b>A.</b> Significantly increased (*p<0.03) cell migration occurred in NF over a 30 hrs period fo...
<p>HaCaT keratinocytes were used to determine the effect of VPA on human keratinocyte migration. Cel...
<p>(A-C) HCFs were scratched and the relative cell migration percentage was quantified at 0, 4, 24, ...
<p>NIH-3T3 fibroblasts were grown to confluency on fibronectin (A&B) or collagen (C) coated coversli...
<p>SW-480 cells in 24-well plates were wounded by scratching with a pipette tip and the cells were i...
<p>Experiments were conducted using PES43 cells. (A) Migration was assayed in 24-well Transwell cham...
<p>Wound healing of human dermal fibroblast monolayers was evaluated by an <i>in vitro</i> scratch a...