Efficient and multiplexed tracking of single cells using whole-body PET/CT.
Hieu T M NguyenNeeladrisingha DasYuting WangCarlos RuvalcabaBrahim MehadjiEmilie RoncaliCharles K F ChanGuillem J PratxPublished in: bioRxiv : the preprint server for biology (2023)
In vivo molecular imaging tools are crucially important for elucidating how cells move through complex biological systems; however, achieving single-cell sensitivity over the entire body remains challenging. Here, we report a highly sensitive and multiplexed approach for tracking upwards of 20 single cells simultaneously in the same subject using positron emission tomography (PET). The method relies on a new tracking algorithm (PEPT-EM) to push the cellular detection threshold to below 4 Bq/cell, and a streamlined workflow to reliably label single cells with over 50 Bq/cell of 18F-fluorodeoxyglucose (FDG). To demonstrate the potential of method, we tracked the fate of over 70 melanoma cells after intracardiac injection and found they primarily arrested in the small capillaries of the pulmonary, musculoskeletal, and digestive organ systems. This study bolsters the evolving potential of PET in offering unmatched insights into the earliest phases of cell trafficking in physiological and pathological processes and in cell-based therapies.
Keyphrases
- positron emission tomography
- pet ct
- single cell
- induced apoptosis
- computed tomography
- cell cycle arrest
- rna seq
- cell therapy
- pet imaging
- cell death
- high throughput
- endoplasmic reticulum stress
- oxidative stress
- machine learning
- bone marrow
- cell proliferation
- atrial fibrillation
- mesenchymal stem cells
- molecularly imprinted
- electronic health record