Abstract

Critical for metabolism, oxygen plays an essential role in maintaining the structure and function of neurons. Oxygen sensing is important in common neurological disorders such as strokes, seizures, or neonatal hypoxic–ischemic injuries, which result from an imbalance between metabolic demand and oxygen supply. Phosphorescence quenching by oxygen provides a non-invasive optical method to measure oxygen levels within cells and tissues. Difluoroboron β-diketonates are a family of luminophores with high quantum yields and tunable fluorescence and phosphorescence when embedded in certain rigid matrices such as poly (lactic acid) (PLA). Boron nanoparticles (BNPs) can be fabricated from dye-PLA materials for oxygen mapping in a variety of biological milieu. These dual-emissive nanoparticles have oxygen-insensitive fluorescence, oxygen-sensitive phosphorescence, and rigid matrix all in one, enabling real-time ratiometric oxygen sensing at micron-level spatial and millisecond-level temporal resolution. In this study, BNPs are applied in mouse brain slices to investigate oxygen distributions and neuronal activity. The optical properties and physical stability of BNPs in a biologically relevant buffer were stable. Primary neuronal cultures were labeled by BNPs and the mitochondria membrane probe MitoTracker Red FM. BNPs were taken up by neuronal cell bodies, at dendrites, and at synapses, and the localization of BNPs was consistent with that of MitoTracker Red FM. The brain slices were stained with the BNPs, and the BNPs did not significantly affect the electrophysiological properties of neurons. Oxygen maps were generated in living brain slices where oxygen is found to be mostly consumed by mitochondria near synapses. Finally, the BNPs exhibited excellent response when the conditions varied from normoxic to hypoxic and when the neuronal activity was increased by increasing K+ concentration. This work demonstrates the capability of BNPs as a non-invasive tool in oxygen sensing and could provide fundamental insight into neuronal mechanisms and excitability research.

Highlights

  • Critical for metabolism, oxygen plays an essential role in maintaining the structure and function of neurons

  • Oxygen is required as a terminal electron acceptor in the aerobic metabolic process, known as oxidative ­phosphorylation[3]. This reaction takes place in mitochondria, during which the electrons transfer from an electron donor to an electron acceptor or oxygen, and energy released from electron flow is used to transform adenosine diphosphate (ADP) to adenosine triphosphate (ATP)

  • Oxygen nanosensors based on phosphorescence quenching can provide information about the brain with improved micron-level spatial and sub-seconds temporal resolution

Read more

Summary

Introduction

Critical for metabolism, oxygen plays an essential role in maintaining the structure and function of neurons. Boron nanoparticles (BNPs) can be fabricated from dye-PLA materials for oxygen mapping in a variety of biological milieu These dualemissive nanoparticles have oxygen-insensitive fluorescence, oxygen-sensitive phosphorescence, and rigid matrix all in one, enabling real-time ratiometric oxygen sensing at micron-level spatial and millisecond-level temporal resolution. Oxygen is required as a terminal electron acceptor in the aerobic metabolic process, known as oxidative ­phosphorylation[3] This reaction takes place in mitochondria, during which the electrons transfer from an electron donor to an electron acceptor or oxygen, and energy released from electron flow is used to transform adenosine diphosphate (ADP) to adenosine triphosphate (ATP). Computed tomography), magnetic resonance techniques (e.g., fMRI), and optical methods based on hemoglobin ­O2 saturation and phosphorescence q­ uenching[15] Some of these methods have significant limitations of equipment cost, invasiveness, or low spatial resolution. Hemoglobinbased detection is indirect and only provides an estimation of ­O2 levels in the blood; and fMRI assessments are restricted to long time scales

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call