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. 2023 Jun 14;39(4):669–679. doi: 10.1007/s43188-023-00195-z

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© The Author(s) under exclusive licence to Korean Society of Toxicology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

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Fig. 3 — AXL regulates cell migration and nutrient-dependent cell death in glioblastoma. a Real-time migration assay of U251-MG using the xCELLigence RTCA DP assay (n = 2) when cultured in fetal bovine serum (FBS)-containing media. The blue line indicates control siRNA-transfected cells, and the black circle indicates AXL siRNA-transfected cells. b Real-time proliferation assay of U251-MG using the xCELLigence RTCA DP assay (n = 2) when cultured in FBS-containing media. The white circle indicates the control siRNA-transfected cells, and the black circle indicates the AXL siRNA-transfected cells. c Real-time proliferation assay of U251-MG using the xCELLigence RTCA DP assay (n = 2) when cultured in FBS-free media. White circle indicated for control siRNA transfected cells and red line indicated for AXL siRNA-transfected cells. d Immunoblot analysis with the indicated antibodies of lysates from U251-MG cells that were transfected with control siRNA or AXL siRNA under epidermal growth factor treatment condition