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1.
Sci Data ; 5: 180237, 2018 11 13.
Article in English | MEDLINE | ID: mdl-30422120

ABSTRACT

Phase contrast time-lapse microscopy is a non-destructive technique that generates large volumes of image-based information to quantify the behaviour of individual cells or cell populations. To guide the development of algorithms for computer-aided cell tracking and analysis, 48 time-lapse image sequences, each spanning approximately 3.5 days, were generated with accompanying ground truths for C2C12 myoblast cells cultured under 4 different media conditions, including with fibroblast growth factor 2 (FGF2), bone morphogenetic protein 2 (BMP2), FGF2 + BMP2, and control (no growth factor). The ground truths generated contain information for tracking at least 3 parent cells and their descendants within these datasets and were validated using a two-tier system of manual curation. This comprehensive, validated dataset will be useful in advancing the development of computer-aided cell tracking algorithms and function as a benchmark, providing an invaluable opportunity to deepen our understanding of individual and population-based cell dynamics for biomedical research.


Subject(s)
Cell Tracking/methods , Algorithms , Animals , Cell Line , Mice , Microscopy, Phase-Contrast , Myoblasts/cytology , Time-Lapse Imaging
2.
PLoS One ; 6(11): e27672, 2011.
Article in English | MEDLINE | ID: mdl-22110715

ABSTRACT

Current cell culture practices are dependent upon human operators and remain laborious and highly subjective, resulting in large variations and inconsistent outcomes, especially when using visual assessments of cell confluency to determine the appropriate time to subculture cells. Although efforts to automate cell culture with robotic systems are underway, the majority of such systems still require human intervention to determine when to subculture. Thus, it is necessary to accurately and objectively determine the appropriate time for cell passaging. Optimal stem cell culturing that maintains cell pluripotency while maximizing cell yields will be especially important for efficient, cost-effective stem cell-based therapies. Toward this goal we developed a real-time computer vision-based system that monitors the degree of cell confluency with a precision of 0.791±0.031 and recall of 0.559±0.043. The system consists of an automated phase-contrast time-lapse microscope and a server. Multiple dishes are sequentially imaged and the data is uploaded to the server that performs computer vision processing, predicts when cells will exceed a pre-defined threshold for optimal cell confluency, and provides a Web-based interface for remote cell culture monitoring. Human operators are also notified via text messaging and e-mail 4 hours prior to reaching this threshold and immediately upon reaching this threshold. This system was successfully used to direct the expansion of a paradigm stem cell population, C2C12 cells. Computer-directed and human-directed control subcultures required 3 serial cultures to achieve the theoretical target cell yield of 50 million C2C12 cells and showed no difference for myogenic and osteogenic differentiation. This automated vision-based system has potential as a tool toward adaptive real-time control of subculturing, cell culture optimization and quality assurance/quality control, and it could be integrated with current and developing robotic cell cultures systems to achieve complete automation.


Subject(s)
Cell Culture Techniques/methods , Cell Engineering/methods , Stem Cells/cytology , Animals , Automation , Cell Line , Cell Proliferation , Humans , Image Processing, Computer-Assisted , Mice , Microscopy , Models, Biological , Time Factors , User-Computer Interface
3.
Article in English | MEDLINE | ID: mdl-22255749

ABSTRACT

The wound healing assay in vitro is widely used for research and discovery in biology and medicine. This assay allows for observing the healing process in vitro in which the cells on the edges of the artificial wound migrate toward the wound area. The influence of different culture conditions can be measured by observing the change in the size of the wound area. For further investigation, more detailed measurements of the cell behaviors are required. In this paper, we present an application of automatic cell tracking in phase-contrast microscopy images to wound healing assay. The cell behaviors under three different culture conditions have been analyzed. Our cell tracking system can track individual cells during the healing process and provide detailed spatio-temporal measurements of cell behaviors. The application demonstrates the effectiveness of automatic cell tracking for quantitative and detailed analysis of the cell behaviors in wound healing assay in vitro.


Subject(s)
Cell Tracking/methods , Microscopy, Phase-Contrast/methods , Microscopy/methods , Neoplasms/pathology , Wound Healing , Algorithms , Animals , Automation , Bridged Bicyclo Compounds, Heterocyclic/pharmacology , Cell Culture Techniques , Cell Line, Tumor , Cell Movement , Cells, Cultured/cytology , Culture Media/pharmacology , Equipment Design , Humans , Imaging, Three-Dimensional , Mitosis , Thiazolidines/pharmacology , Time Factors
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