作者: Natalie L. Prigozhina , Ling Zhong , Edward A. Hunter , Ivana Mikić , Scott Callaway
DOI: 10.1089/ADT.2006.024
关键词:
摘要: Abstract: High throughput image cytometers analyze individual cells in digital photomicrographs by first assigning pixels within each to plasma membrane, cytoplasm, nucleus, or other regions. In this study, we report on a novel algorithm that: 1) identifies membrane regions measure changes membrane-associated proteins (protein kinase C [PKC] α, N-cadherin, E-cadherin, vascular endothelium [VE]-cadherin, and pan-cadherin) that regulate cell division, migration, adhesion 2) delineates the for generalized three-compartment cytometry. Validation assays were performed these cultured 96-well plates also tissue sections obtained from transgenic chemical carcinogenic models of skin cancer. The successfully quantified phorbol 12-myristate 13-acetate (PMA)-induced localization PKCα HeLa (Z′ 0.88). Additionally, PMA activated translocation at P < .01 N-cadherin (in HeLa...