Abstract

.Optogenetics has become an integral tool for studying and dissecting the neural circuitries of the brain using optical control. Recently, it has also begun to be used in the investigation of the spinal cord and peripheral nervous system. However, information on these regions’ optical properties is sparse. Moreover, there is a lack of data on the dependence of light propagation with respect to neural tissue organization and orientation. This information is important for effective simulations and optogenetic planning, particularly in the spinal cord where the myelinated axons are highly organized. To this end, we report experimental measurements for the scattering coefficient, validated with three different methods in both the longitudinal and radial directions of multiple mammalian spinal cords. In our analysis, we find that there is indeed a directional dependence of photon propagation when interacting with organized myelinated axons. Specifically, light propagating perpendicular to myelinated axons in the white matter of the spinal cord produced a measured reduced scattering coefficient () of , and light that was propagated along the myelinated axons in the white matter produced a measured of , across the various species considered. This 50% decrease in scattering power along the myelinated axons is observed with three different measurement strategies (integrating spheres, observed transmittance, and punch-through method). Furthermore, this directional dependence in scattering power and overall light attenuation did not occur in the gray matter regions where the myelin organization is nearly random. The acquired information will be integral in preparing future light-transport simulations and in overall optogenetic planning in both the spinal cord and the brain.

Highlights

  • Optogenetics, the use of light and genetic engineering to probe and manipulate cell activity, is an important emerging technology that is instrumental in decoding the functional organization of brain tissue

  • DePaoli et al.: Anisotropic light scattering from myelinated axons in the spinal cord study behavioral consequences of stimulation in specific classes of neurons under both normal and pathological conditions without confounding effects of genetic ablation or pharmacological intervention.[13,14]

  • We show that light propagation patterns in the spinal cord depend both on the local tissue scattering properties as well as the regional tissue organization

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Summary

Introduction

Optogenetics, the use of light and genetic engineering to probe and manipulate cell activity, is an important emerging technology that is instrumental in decoding the functional organization of brain tissue. The technique has shown promise in the study of the spinal cord and peripheral nervous system.[1,2,3] In the context of motor guidance, optogenetic tools have been used to establish the role played by individual neural populations in motor navigation and have shown potential for restoring function after spinal cord injury or motor neuron disease.[4,5,6,7] In the study of sensory and pain processing, experiments involving targeted optical stimulation have greatly expanded our knowledge about the connectivity and function of peripheral and spinal sensory neurons.[8,9,10,11,12] In vivo control of somatosensory circuits continues to enable researchers to Neurophotonics. Optogenetic control of nerve cell activity relies on the expression of light-sensitive proteins called opsins, which generate depolarizing or hyperpolarizing currents when exposed to light.[15] Cell-selective and temporally precise control over action potential generation in neural circuits, requires a specific knowledge and consideration of the tissue optical properties and illumination profiles

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