QUANTIFICATION OF APOPTOTIC DNA FRAGMENTATION IN A TRANSFORMED UTERINE EPITHELIAL CELL LINE, HRE-H9, USING CAPILLARY ELECTROPHORESIS WITH LASER-INDUCED FLUORESCENCE DETECTOR (CE-LIF)

2001 ◽  
Vol 25 (10) ◽  
pp. 1007-1011 ◽  
Author(s):  
R Fiscus
Keyword(s):  
Capillary Electrophoresis ◽  
Epithelial Cell ◽  
Cell Line ◽  
Dna Fragmentation ◽  
Laser Induced Fluorescence ◽  
Epithelial Cell Line ◽  
Fluorescence Detector ◽  
Uterine Epithelial Cell

scholarly journals Tumor Necrosis Factor α Stimulates MUC1 Synthesis and Ectodomain Release in a Human Uterine Epithelial Cell Line

Endocrinology ◽  
2004 ◽  
Vol 145 (9) ◽  
pp. 4192-4203 ◽  
Author(s):  
Amantha Thathiah ◽  
Melissa Brayman ◽  
Neeraja Dharmaraj ◽  
JoAnne J. Julian ◽  
Errin L. Lagow ◽  
...  
Keyword(s):  
Epithelial Cell ◽  
Cell Line ◽  
Proteolytic Activity ◽  
De Novo ◽  
Embryo Implantation ◽  
Epithelial Cell Line ◽  
Converting Enzyme ◽  
Uterine Epithelial Cell

Abstract Regulation of MUC1 expression and removal is a salient feature of embryo implantation, bacterial clearance, and tumor progression. In some species, embryo implantation is accompanied by a transcriptional decline in uterine epithelial expression of MUC1. In other species, MUC1 is locally removed at blastocyst attachment sites, suggesting a proteolytic activity. Previously, we demonstrated that MUC1 is proteolytically released from the surface of a human uterine epithelial cell line, HES, and identified TNFα converting enzyme/a disintegrin and metalloprotease 17 as a constitutive and phorbol ester-stimulated MUC1 sheddase. The aims of the current study were to test the ability of soluble factors elevated during the periimplantation interval in vivo to stimulate ectodomain shedding of MUC1 from HES uterine epithelial cells and to characterize the nature of this proteolytic activity(ies). We identified TNFα as a prospective endogenous stimulus of MUC1 ectodomain release and of MUC1 and TNFα converting enzyme/a disintegrin and metalloprotease 17 expression. Moreover, we established that TNFα-stimulated MUC1 shedding occurs independently of increased de novo protein synthesis and demonstrated that the TNFα-induced increase in MUC1 gene expression is mediated through the κB site in the MUC1 promoter. Finally, we determined that the TNFα-sensitive MUC1 sheddase is inhibited by the metalloprotease inhibitor, TNFα protease inhibitor (TAPI), and the endogenous tissue inhibitor of metalloprotease-3. Collectively, these studies provide the initial in vitro characterization of a putative physiological stimulus of MUC1 ectodomain release and establish the nature of the metalloproteolytic activity(ies) involved.

An Established Epithelial Cell Line (NPC/HK1) from a Nasopharyngeal Carcinoma - II. A Sem Study

1982 ◽  
Vol 40 ◽  
pp. 224-225
Author(s):  
Li C.L. ◽  
Chew E.C. ◽  
Huang D.P. ◽  
Ho H.C. ◽  
Mak L.S. ◽  
...  
Keyword(s):  
Nasopharyngeal Carcinoma ◽  
Epithelial Cell ◽  
Surface Morphology ◽  
Cell Line ◽  
Epithelial Cell Line ◽  
Present Communication ◽  
Cells In Culture ◽  
Sem Study ◽  
Well Differentiated

An epithelial cell line, NPC/HK1, has recently been successfully established from a nasopharyngeal carcinoma of the moderately to well differentiated squamous type. The present communication reports on the surface morphology of the NPC/HK1 cells in culture.

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