Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
J Biomed Opt ; 19(3): 36004, 2014 Mar.
Article in English | MEDLINE | ID: mdl-24599086

ABSTRACT

Quantification of cell proliferation and monitoring its kinetics are essential in fields of research such as developmental biology, oncology, etc. Although several proliferation assays exist, monitoring cell proliferation kinetics remains challenging. We present a novel cell proliferation assay based on real-time monitoring of cell culture inside a standard incubator using a lensfree video-microscope, combined with automated detection of single cell divisions over a population of several thousand cells. Since the method is based on direct visualization of dividing cells, it is label-free, continuous, and not sample destructive. Kinetics of cell proliferation can be monitored from a few hours to several days. We compare our method to a standard assay, the EdU proliferation assay, and as proof of principle, we demonstrate concentration-dependent and time-dependent effect of actinomycin D-a cell proliferation inhibitor.


Subject(s)
Cell Proliferation , Cytological Techniques/instrumentation , Cytological Techniques/methods , Microscopy, Video/instrumentation , Microscopy, Video/methods , Animals , Cells, Cultured , Kinetics , Mice , NIH 3T3 Cells
2.
Biosens Bioelectron ; 49: 176-83, 2013 Nov 15.
Article in English | MEDLINE | ID: mdl-23747358

ABSTRACT

We present a lensfree imaging method to analyze polarity in RWPE1 prostate epithelial cells that form polarized acini with lumen under standard tridimensional (3D) culture conditions. The first event in epithelial carcinogenesis is loss of polarity, followed by uncontrolled proliferation leading to metastasis. We demonstrate that it is possible to use optical signatures to discriminate 3D objects with distinct polarities in a large field of view. The three metrics we present here are designed as image processing tools to discriminate acini from spheroids without any 3D reconstruction. To demonstrate that our lensfree imaging platform may be used to study the 3D organization of epithelial cells, we analyzed and quantified the modulation of dynamic processes, e.g., the polarity of acini and the merging of polarized structures, upon transforming growth factor beta-1 (TGF beta-1) addition to the culture media. Hence, coupling lensfree microscopy with 3D cell culture provides an innovative tool to study epithelial tissue morphogenesis in a large field of view and to elucidate the regulation of growth, morphogenesis and differentiation in normal and cancerous human prostate cells. Moreover, such biosensor would be a powerful tool to follow cancer progression and to evaluate anti-cancer drugs.


Subject(s)
Acinar Cells/cytology , Epithelial Cells/cytology , Microscopy/instrumentation , Prostate/cytology , Spheroids, Cellular/cytology , Cell Culture Techniques , Cell Line , Cell Line, Tumor , Cell Polarity , Equipment Design , Humans , Image Processing, Computer-Assisted , Male
SELECTION OF CITATIONS
SEARCH DETAIL
...