Poster Session 2.M - Neurosciences
Ms. Somogyi, Fanni, MSc
E58ZQ3
HUN-REN Research Centre for Natural Sciences
06702686813
vereslfanni@gmail.com
Transient protein expression in the brain via lipid nanoparticle-mediated mRNA delivery
Fanni Somogyi1,2, Virág György2, Hella Czigány2,3, Dávid Jólesz2,3, Dániel Hillier2,3
1: János Szentágothai Doctoral School of Neurosciences, Semmelweis University, Budapest, Hungary
2: HUN-REN Research Centre for Natural Sciences, Budapest, Hungary
3: Faculty of Information Technology and Bionics, Pázmány Péter Catholic University, Budapest, Hungary
Poszter
Poster Session 2.M - Neurosciences
English
Neurosciences
Transient protein expression in the brain is desirable when prolonged activity is unnecessary, biologically unfavorable, or experimentally limiting. This is particularly relevant for applications that require short-term protein function and for paradigms in which repeated interventions within the same brain region are advantageous. In this context, mRNA delivery offers a potentially flexible alternative to viral approaches by enabling controlled, non-permanent expression.
Here, we investigate lipid nanoparticle (LNP)-mediated mRNA delivery as a platform for transient protein expression in the brain. We assess selected LNP formulations with respect to delivery performance, expression kinetics, and local tissue response. To characterize these effects, we combine longitudinal in vivo imaging with post hoc histological analysis, allowing us to evaluate protein expression over time alongside markers of immune activation and cellular integrity.
Our findings show that LNP-mediated mRNA delivery can achieve robust but time-limited protein expression in the brain. We further observe formulation-dependent differences in expression efficiency and host response, indicating that nanoparticle composition is a critical determinant of performance in neural tissue. Together, these results support LNP-based mRNA delivery as a promising strategy for transient, localized protein expression in the brain and provide a basis for the further optimization of non-viral gene delivery approaches in neuroscience.
Supported by the following grants: 2019-2.1.7-ERA-NET-2021-00047, the Lendület (“Momentum") Programme of the Hungarian Academy of Sciences, Excellence 151368 from Ministry of Innovation and Technology of Hungary (NRDI fund), CELSA/24/020 and KSZF-161/2024 to DaH. The scientific research and results published here were reached with the sponsorship of Gedeon Richter Talentum Foundation in the framework of Gedeon Richter Excellence PhD Scholarship of Gedeon Richter to FS.
Semmelweis University
Dániel Hillier
I do not give consent to the publication of my abstract on the website of the congress.
in doctoral studies after complex exam (PhD)
Szabad
elfogadva
poszter
nem rendelkezett róla
8099
18:48
18:51