Abstract

Two-photon fluorescence (TPF) microscopy of intrinsic fluorophores provides physiological and pathological information from biological tissues. Reduced nicotinamide adenine dinucleotide (NADH) and flavin adenine dinucleotide (FAD) are two endogenous fluorescent coenzymes existing on the intracellular scale. Autofluorescence images of NADH and FAD have been applied to noninvasively record changes during metabolism, according to their distributions and concentrations. However, the widely used sequential (non-simultaneous) excitation scheme results in artifacts caused by sample motion or laser power fluctuation. The single-wavelength illumination scheme suffers from low excitation efficiency and spectral bleed-through. In this paper, we demonstrate a new imaging system simultaneously capturing autofluorescence images from NADH and FAD, with high excitation efficiency and negligible spectral bleed-through. Two temporally multiplexed and spatially overlapped excitation beams were achieved with fast-switching light paths based on an electro-optic modulator. The switching beams were centered at 750 and 860 nm, enabling independent excitations of NADH and FAD. Autofluorescence images of NADH and FAD were acquired at the wavelength ranges of 415–455 nm and 500–550 nm, respectively. The electro-optic modulator was synchronized with the pixel clock from the microscope, achieving pixel-to-pixel wavelength-switching. The capability of the system was demonstrated by performing TPF imaging of freshly excised mouse colon tissues. The microenvironment of the colon wall was depicted by the distributions of colonocytes, goblet cells, and crypts of Lieberkühn, and the relative concentrations of NADH and FAD were estimated. The experimental results show that the system can effectively perform simultaneous imaging of NADH and FAD, and is considered a promising tool for investigations into metabolism-associated processes and diseases.

Highlights

  • Two-photon fluorescence (TPF) microscopy has been proven to be a powerful technique for imaging in biological tissues [1]

  • We first demonstrate the capability of the imaging system in NADH and flavin adenine dinucleotide (FAD) solutions

  • If a mixture of both NADH and FAD is applied as the specimen, the excitation/detection combination of 750/500–550 nm is not suitable for imaging NADH or FAD anymore, because of severe spectral bleed-through (SBT)

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Summary

Introduction

Two-photon fluorescence (TPF) microscopy has been proven to be a powerful technique for imaging in biological tissues [1]. TPF microscopy is a label-free technique because the existence of endogenous fluorophores in biological tissues eliminates the need for exogenous biomarkers for imaging. The advantage is that autofluorescence signals of NADH and FAD can be completely separated, and misinterpretation can be avoided during analysis. It suffers from low acquisition speed and artifacts from sample motion or laser power fluctuation when tuning between two wavelengths. Another scheme using single-wavelength (e.g., 800 nm) excitation can excite NADH and FAD simultaneously at the cost of unavoidable spectral bleed-through (SBT) and low excitation efficiency [8]

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