[Thèse - 2024] Focused ultrasound neurostimulation for chronic pain treatment

Date de soutenance : 01/04/2024

Equipe associée :
Équipe Ondes et Imagerie


Keywords: Ultrasound neurostimulation, chronic pain, in vivo neuroimaging, cell lineage, FOS-TRAP mice, RNA-sequencing 

Focused ultrasound neurostimulation for chronic pain treatment

*** CENTURI PhD program at Aix-Marseille University (LMA/IBDM/FRESNEL)

Abstract

Focused ultrasound (US) neurostimulation is a promising alternative technique for chronic pain treatment. The advantages of US neurostimulation compared to standard electrical stimulation are non-invasiveness, deep-penetration and high spatiotemporal accuracy. Our recent in vitro study in mouse dorsal root ganglia (DRG) neurons demonstrated that a specific class of mechanoreceptors (termed the low-threshold C-mechanoreceptors C-LTMRs) is potently excited by ultrasound than any other class. Interestingly, the C-LTMRs have been identified as strong modulators of injury-induced pain, suggesting that this particular class of neurons is likely to constitute an important, yet unexplored, target for the treatment of chronic pathological pain. The aim of this interdisciplinary PhD project is to explore the US-induced stimulation of C-LTMRs in mice in vivo and to identify the sensory pathways triggered by US stimuli using optical imaging techniques (multi-photon microscopy and/or photoacoustic tomography) in combination with molecular readouts all along the pain pathway. This will pave the way to a new generation of therapeutic ultrasound device for pain treatment.

Objectives 
The first objective of the Centuri PhD project is to explore the US-induced stimulation of C-LTMRs in mice in vivo. Following our previous in vitro demonstration that C-LTMRs are sensitive to US stimulation, we propose to stimulate skin in mice in vivo and identify the sensory pathways triggered by US stimuli using optical imaging techniques (multi-photon microscopy and/or photoacoustic tomography). The second objective will be to understand the physical mechanisms by which US activate C-LTMRs by developing an in vitro device for measuring the effects of focused US on 3D neuronal cell models.

Proposed approach
The mechanosensory DRG neurons that innervate the skin transmit sensory information to a complex network of neurons in the dorsal horn of the spinal cord, where this information is processed. Then this information is relayed to the somatosensory cortex for integration and perception. The skin of FOS-TRAP mouse (available at IBDM) will be sonicated by focused US. The US-activated circuit will first be identified thanks to the genetic marking of the trapped neurons at the DRGs, spinal cord and brain levels. We will then investigate several combinations of US parameters in vivo to identify efficient and reliable US protocol to stimulate DRGs (and peculiarly targeted C-LTMRs) by using optical neuroimaging techniques. Finally, the molecular and functional identities of the trapped neurons will be unraveled using FACS sorting followed by single cell RNA-sequencing.  The physical mechanisms will be quantified by conducting in vitro experiments on 3D neuronal cell models to assess the deformation of cells/nerves due to acoustic radiation force during US stimulation. 

Interdisciplinarity
This project will combine the strengths of three Centuri laboratories at the interface of physics and biology with complementary skills: the LMA with an expertise in ultrasonic imaging and neurostimulation, the IBDM in molecular biology of mechanosensory neurons and the Fresnel Institute in optical imaging of neuronal activity.
The LMA (Franceschini group) is developing experimental approaches and applying physical concepts to achieve a quantitative understanding of physical mechanisms of US-induced neurostimulation. The IBDM (Moqrich group) is expert in the functional significance of primary sensory neurons in chronic pain, who will contribute to the understanding of molecular mechanisms and of sensory pathways triggered by US stimuli. The Fresnel institute (Rigneault – Chaigne group) is developing advanced optical neuroimaging techniques, enabling in vivo monitoring of neuronal activity by using multi-photon microscopy and/or photoacoustics.

PhD student’s expected profile
The PhD candidate should hold a MSc (or equivalent degree) in physics, biophysics, acoustics, molecular or cellular biology, neurosciences or a related discipline. We aim to find a highly-motivated student with creative skills and appeal for experimental work. Ability to work in an interdisciplinary environment involving several research teams will be required. Some good English language skills and profusion in data analysis using, e.g. Matlab, will be a strong plus.

More information & References related to the project here

 

lien PDF
Voir le PDF