| Literature DB >> 25360383 |
Youbo Zhao1, Marina Marjanovic1, Eric J Chaney1, Benedikt W Graf2, Ziad Mahmassani3, Marni D Boppart3, Stephen A Boppart4.
Abstract
We demonstrate real-time, longitudinal, label-free tracking of apoptotic and necrotic cells in living tissue using a multimodal microscope. The integrated imaging platform combines multi-photon microscopy (MPM, based on two-photon excitation fluorescence), optical coherence microscopy (OCM), and fluorescence lifetime imaging microscopy (FLIM). Three-dimensional (3-D) co-registered images are captured that carry comprehensive information of the sample, including structural, molecular, and metabolic properties, based on light scattering, autofluorescence intensity, and autofluorescence lifetime, respectively. Different cell death processes, namely, apoptosis and necrosis, of keratinocytes from different epidermal layers are longitudinally monitored and investigated. Differentiation of the two cell death processes in a complex living tissue environment is enabled by quantitative image analysis and high-confidence classification processing based on the multidimensional, cross-validating imaging data. These results suggest that despite the limitations of each individual label-free modality, this multimodal imaging approach holds the promise for studies of different cell death processes in living tissue and in vivo organs.Entities:
Keywords: (170.1530) Cell analysis; (170.1870) Dermatology; (170.4500) Optical coherence tomography; (180.2520) Fluorescence microscopy; (180.4315) Nonlinear microscopy
Year: 2014 PMID: 25360383 PMCID: PMC4206335 DOI: 10.1364/BOE.5.003699
Source DB: PubMed Journal: Biomed Opt Express ISSN: 2156-7085 Impact factor: 3.732