|Kahl, Stanislaw - Stass|
|KERR, DAVID - University Of Vermont|
|ZUDAIRE, ENRIQUE - National Cancer Institute (NCI, NIH)|
|CUTTITTA, FRANK - National Cancer Institute (NCI, NIH)|
Submitted to: Meeting Abstract
Publication Type: Abstract Only
Publication Acceptance Date: 3/19/2014
Publication Date: 7/18/2014
Citation: Elsasser, T.H., Kahl, S., Kerr, D., Zudaire, E., Cuttitta, F. 2014. Proinflammatory responses of a hTERT-transformed, immortalized line of cultured bovine mammary epithelial cells (BME). Meeting Abstract. 65.
Technical Abstract: Primary cultures BME were generated from healthy mammary glands as described (Vet Immunol Immunopath 101(3-4):191-202, 2004). Towards immortalization, BME from four cows were pooled and transfected with pCI neo-hEST2-HA , a human telomerase segment containing a neomycin/Geneticin resistance selection cassette (Cell 90:785-95, 1997). Cells were grown in DMEM +10%FBS and Geneticin (800 microgram/ml) and followed through the ensuing selection growth lag to full proliferation capacity. Following 50+ passages, cells were further subcloned to increase epithelial and decrease myoepithelial cell content; the resulting culture was called ELS-321-Clone2B. For function studies and to achieve hormone and cytokine receptor access by the apical-lumenal polarized cells, cultures experiments were conducted on porous (0.4 micron) hanging well inserts coated with laminin-111. At confluence, cells had the following characteristics: tight junctions (electron microscopic confirmation of desmosomes, EpCAM-1 and E-cadherin immunostaining), expression (immunohistochemical localization ) of prolactin receptor PRLr, xanthine oxidase (XO), inducible nitric oxide synthase (iNOS), and cytokeratin-18 (<10% cells displayed myoepithelial smooth muscle actin).