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1.
J Clin Microbiol ; 50(5): 1762-3, 2012 May.
Article in English | MEDLINE | ID: mdl-22378909

ABSTRACT

A novel fecal antigen detection assay for fresh and frozen human samples that detects but does not differentiate Giardia spp, Cryptosporidium spp, and Entamoeba histolytica, the Tri-Combo parasite screen, was compared to three established enzyme-linked immunosorbent assays (ELISAs) at three international sites. It exhibited 97.9% sensitivity and 97.0% specificity, with positive and negative predictive values of 93.4% and 99.1%, respectively. The Tri-Combo test proved a reliable means to limit the use of individual parasite ELISAs to positive samples.


Subject(s)
Antigens, Protozoan/analysis , Clinical Laboratory Techniques/methods , Cryptosporidium/isolation & purification , Entamoeba histolytica/isolation & purification , Feces/parasitology , Giardia/isolation & purification , Parasitology/methods , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Enzyme-Linked Immunosorbent Assay/methods , Female , Humans , Infant , Male , Middle Aged , Sensitivity and Specificity , Young Adult
2.
PLoS One ; 10(2): e0116755, 2015.
Article in English | MEDLINE | ID: mdl-25714835

ABSTRACT

Co-culture of human primary epithelial cells with irradiated 3T3 fibroblast feeder cells (J2 cells) and the Rho kinase inhibitor Y-27632 (Y) allows for the unrestricted growth of cells of epithelial origin by the process termed conditional reprogramming. To better understand the nature of the signaling processes associated with conditionally reprogrammed cells, the effect of the two critical components of the co-culture conditions, J2 cells and Y, on the growth of human foreskin keratinocytes (HFKs) was evaluated by gene expression profiling, reverse-phase protein arrays and siRNA screening. J2 cells and Y acted cooperatively to down-regulate differentiation, and upregulate proliferation and cell adhesion, including increased pT308Akt and pERK, and reduced TGF-ß pathway signaling. These findings establish a mechanistic basis for the unlimited growth potential of human epithelial cells that will be invaluable to assess the effect of genetic changes in pathologic tissues and their response to therapeutic agents.


Subject(s)
Cellular Reprogramming , Keratinocytes/cytology , Keratinocytes/metabolism , Amides/pharmacology , Animals , Cell Adhesion , Cell Cycle/drug effects , Cell Differentiation/drug effects , Cell Line , Cell Proliferation , Cells, Cultured , Cluster Analysis , Coculture Techniques , Feeder Cells , Gene Expression Profiling , Gene Expression Regulation , Humans , Keratinocytes/drug effects , Protein Processing, Post-Translational , Pyridines/pharmacology , RNA, Small Interfering
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