| Literature DB >> 26451599 |
Inka Regine Weingaertner, Sarah Koutnik, Hermann Ammer.
Abstract
Entities:
Year: 2015 PMID: 26451599 PMCID: PMC4599909 DOI: 10.1371/journal.pone.0140727
Source DB: PubMed Journal: PLoS One ISSN: 1932-6203 Impact factor: 3.240
Fig 2Regulation of BT474 cell growth and migration by Morphine.
(A) BT474 cells were cultured for 5 d in the presence or absence of Morphine (10 μM), Naloxone (100 μM), and Heregulin (40 ng/ml), before cell growth was determined by crystal violet staining. Top: Photograph of tissue culture wells from a representative experiment before solubilisation of the dye. Bottom: Data of n = 6 independent experiments normalized to controls. Note that co-incubation of the cells with Morphine significantly attenuates Heregulin-stimulated cell growth (**, p < .005). (B) BT474 cell migration was assessed by the scratch assay done in cells grown for 5 d in the absence (control) or presence of Heregulin (40 ng/ml), Morphine (10 μM) and Naloxone (100 μM) as indicated. After scratching, cells were kept for another 24 h in the presence of the above ligands, before images were acquired using an Olympus BH-2 microscope (40× magnification). The figures shown are representative for 3 independent experiments yielding qualitatively similar results.