Wnt-5a Signaling Mediates Metaplasticity at Hippocampal CA3-CA1 Synapses in Mice


Por: Parodi, J, Mira, RG, Fuenzalida, M, Cerpa, W, Serrano, FG, Tapia-Rojas, C, Martinez-Torres, A, Inestrosa, NC

Publicada: 1 dic 2024
Resumen:
Wnt signaling plays a role in synaptic plasticity, but the specific cellular events and molecular components involved in Wnt signaling-mediated synaptic plasticity are not well defined. Here, we report a change in the threshold required to induce synaptic plasticity that facilitates the induction of long-term potentiation (LTP) and inhibits the induction of long-term depression (LTD) during brief exposure to the noncanonical ligand Wnt-5a. Both effects are related to the metaplastic switch of hippocampal CA3-CA1 synaptic transmission, a complex mechanism underlying the regulation of the threshold required to induce synaptic plasticity and of synaptic efficacy. We observed an early increase in the amplitude of field excitatory postsynaptic potentials (fEPSPs) that persisted over time, including after washout. The first phase involves an increase in the fEPSP amplitude that is required to trigger a spontaneous second phase that depends on Jun N-terminal kinase (JNK) and N-methyl D-aspartate receptor (NMDAR) activity. These changes are prevented by treatment with secreted frizzled-related protein 2 (sFRP-2), an endogenous antagonist of Wnt ligands. Here, we demonstrate the contribution of Wnt-5a signaling to a process associated with metaplasticity at CA3-CA1 synapses that favors LTP over LTD.

Filiaciones:
Parodi, J:
 Univ Autonoma Chile, Fac Ciencias Sociales & Humanidades, Dept Anal Datos, Temuco 4810101, Chile

Mira, RG:
 Univ Magallanes, Escuela Med, Ctr Excelencia Biomed Magallanes CEBIMA, Punta Arenas, Chile

Fuenzalida, M:
 Univ Valparaiso, Ctr Neurobiol & Fisiopatol Integrat CENFI, Inst Fisiol, Valparaiso Millenium Nucleus Neuroepigenet & Plast, Santiago, Valparaiso, Chile

Cerpa, W:
 Pontificia Univ Catolica Chile, Fac Ciencias Biol, Dept Biol Celular & Mol, Santiago, Chile

Serrano, FG:
 Pontificia Univ Catolica Chile, Fac Ciencias Biol, Dept Biol Celular & Mol, Santiago, Chile

Tapia-Rojas, C:
 Univ San Sebastian, Fdn Ciencia & Vida, Fac Med & Ciencia, Ctr Cientif & Tecnol Excelencia Ciencia & Vida, Santiago, Chile

Martinez-Torres, A:
 Univ Nacl Autonoma Mexico, Inst Neurobiol, Dept Neurobiol Celular & Mol, Queretaro, Mexico

Inestrosa, NC:
 Univ Magallanes, Escuela Med, Ctr Excelencia Biomed Magallanes CEBIMA, Punta Arenas, Chile

 Pontificia Univ Catolica Chile, Fac Ciencias Biol, Dept Biol Celular & Mol, Santiago, Chile
ISSN: 02724340
Editorial
Kluwer Academic Publishers-Plenum Publishers, 233 SPRING ST, NEW YORK, NY 10013 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 44 Número: 1
Páginas:
WOS Id: 001353706300001
ID de PubMed: 39535658
imagen hybrid, Green Accepted, All Open Access; Green Open Access; Hybrid Gold Open Access

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