Senior Staff Scientist Waters BioSciences Milpitas, California, United States
Disclosure(s):
Xiaoshan Shi, PhD: No relevant disclosure to display
Introduction/Rationale: T cells have critical roles in immune response to infections, tumors, and other pathologies, and their efficacy is rooted in their functional and metabolic status. Mitochondria are important intracellular organelles intertwined with T cell metabolism and function. Upon T cell activation, mitochondria undergo dynamic remodeling marked by a series of structural changes associated with efficient electron transport and metabolic transitions. Failure to induce these metabolic changes can prevent T cell proliferation, activation and effector function. Although mitochondrial structure and metabolic programs are of wide interest to researchers, tools for rapidly assessing T cell mitochondrial morphology together with other phenotypic features remain limited.
Methods: Currently, researchers utilize various microscopy techniques to visualize mitochondria, which is technically demanding and can be biased due to limited number of images available for analysis. In this study, we addressed this technical gap by leveraging high-speed imaging flow cytometry to enable interrogation of mitochondrial dynamics in T cells.
Results: Using an in vitro system of T-cell activation that recapitulated increases in the number and volume of mitochondria, we identified unique mitochondrial phenotypes using a high-speed imaging flow cytometer. A set of intuitive spatial image parameters were examined to select ideal parameters based on unsupervised clustering. Using these imaging parameters, we quantified and sorted T cells with distinct mitochondrial morphology at high speed. Subsequent transcriptomic characterization revealed metabolic heterogeneity associated with distinct mitochondrial phenotypes, validating the new imaging flow cytometry and cell sorting method.
Conclusion: This work develops a high-throughput method to characterize phenotypic variation in mitochondrial morphology, and provides a workflow integrating cell activation, sorting, and transcriptomics to elucidate mechanisms underlying mitochondrial dynamics.
