Title :
Cell migration imaging and its functional analysis
Author :
Kushibiki, Toshihiro ; Eda, Hideo ; Sano, Tomoko ; Awazu, Kunio
Author_Institution :
Osaka Univ., Osaka
Abstract :
In this study, a new type of cell-cultivation system based on laser processing has been developed for the on-chip cultivation of living cells. We introduce a "laser cell-chip". A sheet prepared from epoxy resin was processed by KrF excimer laser (248 nm, 1.6 J/cm2) for preparation of microgrooved surfaces with various groove width, spacing, and depth. A laser cell-chip can make kinetic studies of cell migration depending on the concentration gradient of a chemoattractant. In this study, megakaryocytes were used for the migration on a groove of laser cell-chip by the concentration gradient of the stromal cell derived factor 1 (SDF-1/CXCL12). SDF-1/CXCL12 plays an important and unique role in the regulation of stem/progenitor cell trafficking. A megakaryocyte was migrated on a groove of laser cell-chip depending on the optical concentration gradient of SDF-1/CXCL12. However, SDF-1-induced cell migration was inhibited by the pretreatment of phosphatidylinositol 3-kinase (PI3K) inhibitor, wortmannin and LY294002, suggesting that PI3K is likely involved in SDF-1-induced megakaryocyte migration. It is concluded that "laser cell-chip" was useful for the screening assay for migratory/antimigratory compounds.
Keywords :
biochemistry; biology computing; cell motility; lab-on-a-chip; laser beam applications; cell migration imaging; cell-cultivation system; epoxy resin; functional analysis; laser cell-chip; laser processing; megakaryocytes; microgrooved surfaces; phosphatidylinositol 3-kinase inhibitor; wavelength 248 nm; Biochemical analysis; Cells (biology); Chemical lasers; Functional analysis; Metastasis; Microstructure; Power engineering and energy; Stem cells; Tumors; White blood cells; cell migration; chemoattractant; laser cell-chip; megakaryocyte; stromal cell derived factor 1 (SDF-1/CXCL12);
Conference_Titel :
Automation Congress, 2006. WAC '06. World
Conference_Location :
Budapest
Print_ISBN :
1-889335-33-9
DOI :
10.1109/WAC.2006.375758