# Monitoring neurochemical signaling dynamics in the lymph node

> **NIH NIH R01** · UNIVERSITY OF CINCINNATI · 2024 · $392,085

## Abstract

PROJECT SUMMARY
Neurochemical signaling within immune organs, like the lymph node, remains challenging to probe with existing
technology yet knowing the mechanisms and function of this signaling would positively impact our understanding
of immunity. Our long-term goal is to understand neurochemical regulated immunity during inflammation,
autoimmunity, and even depression. To achieve this goal, new analytical tools are needed which can capture rapid
neurochemical signaling in intact immune organs with high spatial resolution. The specific objective of this proposal
is to develop and validate methods using fast-scan cyclic voltammetry (FSCV) at carbon-based microelectrodes to
detect norepinephrine, ATP, and melatonin in slices of the mesenteric lymph node (mLN). All three neurochemicals
are important for either triggering or suppressing immune responses within the gut-immune system; however, the
dynamics and mechanisms by which they function are not understood. The rationale for this proposal is that the
development of new tools to monitor rapid neurochemical signaling in an intact mLN will provide knowledge of
neuroimmune communication dynamics in the gut which could lead to sophisticated neurochemical-targeted
therapies for gastrointestinal inflammation and an improved understanding of the gut-brain axis. The proposal will
be completed by the following three specific aims: (1) Develop innovative electrochemical methods to detect and
validate neuronal norepinephrine release in live mLN slices, (2) Develop anion-exchange doped carbon-fiber
microelectrodes for sensitive ATP detection in the mLN, and (3) Develop fouling-resistant sensors for multiplexed
detection of melatonin with catecholamines in the mLN. We will pursue these aims with an innovative approach
combining the power of fast-scan cyclic voltammetry’s high temporal resolution and spatial resolution with detection
in live slices of the lymph node. This work is also innovative because new carbon electrodes and surface
chemistries will be developed for targeted-analyte detection. This work is significant because the tools developed
will help shift the paradigm that immunomodulation is slow and will impact our understanding of neuroimmune
communication mechanisms and dynamics, specifically within the gut-immune system. Tools to detect rapid
concentrations fluctuations in norepinephrine, ATP, and melatonin are also significant because they are not only
involved in immunomodulation in the immune system, but are heavily involved in signaling throughout the body.
The tools are translatable to any biological system. The expected outcome is a new toolbox for high temporal
resolution detection of neurochemicals in the lymph node which will lead to an improved understanding of the
mechanism and function of neurochemical signaling in spatially-resolved regions of mLN during conditions of health
and inflammation. This work will have a positive impact on how neuroimmune communication is studied, and wil...

## Key facts

- **NIH application ID:** 10906750
- **Project number:** 5R01AI151552-05
- **Recipient organization:** UNIVERSITY OF CINCINNATI
- **Principal Investigator:** Ashley E Ross
- **Activity code:** R01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $392,085
- **Award type:** 5
- **Project period:** 2020-09-14 → 2026-08-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10906750

## Citation

> US National Institutes of Health, RePORTER application 10906750, Monitoring neurochemical signaling dynamics in the lymph node (5R01AI151552-05). Retrieved via AI Analytics 2026-05-23 from https://api.ai-analytics.org/grant/nih/10906750. Licensed CC0.

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