El lactato extracelular mejora la neurogénesis mediante la modulación de la lactilación de H3K9 y la expresión de
Wenhong Xu1, Anqi Zhao1, Rui Han2
1The Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun, 130021, China.
Stem cell research & therapy
|August 27, 2025
Resumen
El L-lactato promueve la neurogénesis a través de la lactilación de histonas (H3K9la) y la proteína SnoN bajo hipoxia. Esta vía destaca objetivos terapéuticos potenciales para la recuperación neurológica.
Área de la Ciencia:
- La neurociencia
- La bioquímica
- Biología de las células madre
Sus antecedentes:
- El lactato beneficia la neurogénesis en adultos y media la lactilación de proteínas.
- El papel de la lactilación histónica en la neurogénesis no se comprende bien.
- La investigación del impacto del lactato en las células madre neurales (CNS) y la lactilación histónica es crucial.
Objetivo del estudio:
- Para aclarar la relación entre el lactato y el destino NSC.
- Para explorar la función de la lactilación histónica en la neurogénesis.
Principales métodos:
- Los NSC fueron tratados con lactato en condiciones hipóxicas.
- Se emplearon Western blot, inmunofluorescencia, secuenciación de ARN y secuenciación de ChIP.
- Se analizaron las modificaciones de la lactilación de histonas y los cambios en la expresión génica.
Principales resultados:
- El L-lactato promovió la neurogénesis e indujo la lactilación de la histona H3K9 (H3K9la) bajo hipóxia.
- La inhibición del L-lactato o de la H3K9la altera el desarrollo neuronal y la diferenciación de los NSC.
- H3K9la se enriqueció en el promotor de SnoN, y la inhibición de SnoN redujo la generación de neuronas de Doublecortin (DCX).
Conclusiones:
- El L-lactato promueve la neurogénesis a través de la vía H3K9la/SnoN en condiciones hipóxicas.
- El SnoN se identifica como un mediador clave en la neurogénesis inducida por el lactato.
- El eje H3K9la/SnoN presenta un objetivo terapéutico potencial para la recuperación neurológica, particularmente en la isquemia cerebral.
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