Carregant...
Tipus de document
Treball de fi de grauData de publicació
Llicència de publicació
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/199965
Optimization of SH-SY5Y Differentiation to Study Neuronal Mechanosensitivity
Títol de la revista
Autors
Director/Tutor
ISSN de la revista
Títol del volum
Recurs relacionat
Resum
Neurodegenerative disorders, including Alzheimer’s disease, pose a global social burden strongly
linked with aging populations. Despite extensive research efforts, the underlying causes of the
neuropathological changes that result in neuronal death are unknown, making the improvement of
in vitro models a priority to address. Moreover, these pathological events are accompanied by
alterations in brain rigidity, and while it is well established how various cell types can feel these
mechanical cues and adapt their function, neuronal mechanosensing remains mostly unexplored.
For this reason, in this project we aimed to investigate the mechanobiology of Alzheimer's disease
by optimizing the differentiation of SH-SY5Y cells into pseudo-neurons.
To facilitate neuronal differentiation, we adopted a novel strategy in which, by introducing a genetic
construct in the SH-SY5Y cells, we could control the expression of the neuronal master gene
NGN2. We demonstrated that this system, along with an optimized differentiation protocol, led to
the production of more mature neuron-like cells.
Subsequently, the response of differentiated cells to mechanical stimulation was tested by culturing
them in polyacrylamide gels with varying stiffness. Immunostaining and image analysis confirmed
the morphological adaptation of neuron-like cells to matrix stiffness, presenting better morphology
at a higher stiffness. Finally, we observed detectable levels of the co-transcriptional factor YAP and
confirmed that its nuclear presence is mechanoregulated in neurons.
In conclusion, by combining differentiation techniques, genetic modification, and mechanical
stimulation, our study provides a new model to explore Alzheimer's disease mechanobiology,
potentially leading to innovative therapeutic strategies by uncovering complex underlying
mechanisms.
Descripció
Treballs Finals de Grau d'Enginyeria Biomèdica. Facultat de Medicina i Ciències de la Salut. Universitat de Barcelona. Curs: 2022-2023. Tutor/Director: Roca-Cusachs Soulere, Pere, De la Cruz, Jorge Oliver
Matèries (anglès)
Citació
Citació
HINOJOSA GRAJALES, Yara. Optimization of SH-SY5Y Differentiation to Study Neuronal Mechanosensitivity. [consulta: 5 de febrer de 2026]. [Disponible a: https://hdl.handle.net/2445/199965]