PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
This study employs the optical redox ratio and fluorescence lifetime imaging microscopy of intrinsic metabolic coenzymes NAD(P)H and FAD to assess the metabolic state of human neutrophils in vitro, under a variety of activation conditions and targeted metabolic pathway inhibition at the single-cell level. By measuring effector functions such as oxidative burst, neutrophil activation could be confirmed. In addition, identical metabolic changes were detected in zebrafish larvae neutrophils following activation, confirming the validity of these findings in vivo.
Rupsa Datta
"Optical metabolic imaging of neutrophil activation and effector function", Proc. SPIE PC12847, Multiphoton Microscopy in the Biomedical Sciences XXIV, PC128470Q (13 March 2024); https://doi.org/10.1117/12.3001813
ACCESS THE FULL ARTICLE
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Rupsa Datta, "Optical metabolic imaging of neutrophil activation and effector function," Proc. SPIE PC12847, Multiphoton Microscopy in the Biomedical Sciences XXIV, PC128470Q (13 March 2024); https://doi.org/10.1117/12.3001813