# Investigating Neuromelanin-Mediated Locus Coeruleus Neurodegeneration in a Novel Mouse Model of Parkinson's Disease > **NIH NIH F99** · EMORY UNIVERSITY · 2022 · $45,556 ## Abstract Investigating neuromelanin-mediated locus coeruleus neurodegeneration in a novel mouse model of Parkinson’s disease Alexa Iannitelli Summary Parkinson’s disease (PD) is the second most common neurodegenerative disorder worldwide, and is characterized by motor and non-motor symptoms. The leading pharmacotherapy, levodopa, is only effective for treating the motor symptoms caused by dopamine (DA) neuron degeneration, while non-motor symptoms associated with noradrenergic dysfunction have grave consequences for the quality of life experienced by PD patients and are not alleviated by any currently available therapies. Thus, new research on PD neuropathology and treatment must consider the locus coeruleus (LC), the major central noradrenergic nucleus. The LC develops alpha-synuclein pathology prior to DA neurons in PD and is almost completely degenerated in later stage disease, but the molecular mechanisms responsible for its vulnerability are unknown. Along with substantia nigra DA neurons, the LC is the only structure in the brain that produces appreciable amounts of neuromelanin (NM), a dark brown cytoplasmic pigment. It has been proposed that these NM granules initially play a protective role by sequestering toxic catecholamine metabolites and heavy metals, but become harmful during aging and particularly in PD as they overwhelm cellular machinery and get released during neurodegeneration. Because rodents do not naturally produce NM, the study of this pigment has been mostly limited to human postmortem studies, and it has not been possible to experimentally address the role of NM in PD-associated LC pathology. However, I have adapted a viral-mediated approach for expression of human tyrosinase, the enzyme responsible for the development of melanin in skin cells, to promote NM production in rodent LC neurons. I found that pigment expression in the LC recapitulates key features of endogenous NM found in primates, including eumelanin and pheomelanin, lipid droplets, and a double-membrane encasement. By 10-weeks post-injection, mice display severe LC neurodegeneration and a robust neuroinflammatory response, resulting in astrocytic glial scarring. Behavioral consequences include hyperarousal, increased anxiety-like behavior, and cognitive impairment. These phenotypes reflect non-motor symptoms of PD, validating the utility of this model for studying the consequences of NM accumulation in the LC as it relates to neurodegenerative disease. During the F99 phase, I propose to expand these findings by employing the ribo-tagging technique Translating Ribosome Affinity Purification (TRAP) to investigate how changes in gene transcription relate to, and potentially underlie, NM-induced LC dysfunction and degeneration. In the K00 phase, I will apply the information gleaned from these studies to investigate potential mechanistic and pharmacological interventions in the hopes of mitigating toxic NM accumulation and subsequent neurodegeneration, in both the LC and ... ## Key facts - **NIH application ID:** 10541704 - **Project number:** 1F99NS129168-01 - **Recipient organization:** EMORY UNIVERSITY - **Principal Investigator:** Alexa Faith Iannitelli - **Activity code:** F99 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2022 - **Award amount:** $45,556 - **Award type:** 1 - **Project period:** 2022-07-01 → 2023-05-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10541704 ## Citation > US National Institutes of Health, RePORTER application 10541704, Investigating Neuromelanin-Mediated Locus Coeruleus Neurodegeneration in a Novel Mouse Model of Parkinson's Disease (1F99NS129168-01). Retrieved via AI Analytics 2026-06-01 from https://api.ai-analytics.org/grant/nih/10541704. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*