2014
DOI: 10.3791/51963
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Analysis of Cell Migration within a Three-dimensional Collagen Matrix

Abstract: The ability to migrate is a hallmark of various cell types and plays a crucial role in several physiological processes, including embryonic development, wound healing, and immune responses. However, cell migration is also a key mechanism in cancer enabling these cancer cells to detach from the primary tumor to start metastatic spreading. Within the past years various cell migration assays have been developed to analyze the migratory behavior of different cell types. Because the locomotory behavior of cells mar… Show more

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Cited by 24 publications
(20 citation statements)
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“…The analysis of the migratory activity within a 3D collagen matrix was performed as described [ 22 , 25 ]. In brief, 4×10 6 cells were resuspended in 50 μL medium, which was thoroughly mixed with 100 μL collagen solution composed of liquid collagen (PureCol; Nutacon BV, Leimuiden, The Netherlands), 10× minimal essential medium (Sigma-Aldrich, Taufkirchen, Germany) and 7.5% sodium bicarbonate solution (Sigma-Aldrich, Taufkirchen, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…The analysis of the migratory activity within a 3D collagen matrix was performed as described [ 22 , 25 ]. In brief, 4×10 6 cells were resuspended in 50 μL medium, which was thoroughly mixed with 100 μL collagen solution composed of liquid collagen (PureCol; Nutacon BV, Leimuiden, The Netherlands), 10× minimal essential medium (Sigma-Aldrich, Taufkirchen, Germany) and 7.5% sodium bicarbonate solution (Sigma-Aldrich, Taufkirchen, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…To do this, we specifically examined the phosphorylation of tyrosine-1248 residue of HER2 which is tightly linked to oncogenic transformation and the ras/ mitogen activated protein (MAP) kinase signaling pathway [27]. Apparently, anti-HER2his-scFv treatment blocked the heregulindependent phosphorylation of the expressed HER2 in SK-OV-3 cells, as shown in Fig.…”
Section: Bioactivity Of Anti-her2his-scfvmentioning
confidence: 97%
“…Then, cells were stained with AlexaFluor 488-phalloidin and DAPI and analysed by confocal microscopy. For live cell imaging in 3D collagen, we built chambers, as described by Rommerswinkel et al (2014), placed 150 µl of collagen solution into these chambers, polymerised collagen for 1 h at 37°C and analysed cell motility using Nikon Еclipse Ti-E microscope.…”
Section: (D) Migration In 3d Collagen Gelmentioning
confidence: 99%