Por favor, use este identificador para citar o enlazar este ítem: https://doi.org/10.14670/HH-18-625

Título: Plexin-mediated neuronal development and neuroinflammatory responses in the nervous system
Fecha de publicación: 2023
Editorial: Universidad de Murcia, Departamento de Biologia Celular e Histiologia
Cita bibliográfica: Histology and Histopathology Vol. 38, nº11 (2023)
ISSN: 0213-3911
1699-5848
Materias relacionadas: CDU::6 - Ciencias aplicadas::61 - Medicina::616 - Patología. Medicina clínica. Oncología
Palabras clave: Plexins
Glioma
Neurodevelopment
Neuroinflammation
Resumen: Plexins are a large family of single-pass transmembrane proteins that mediate semaphorin signaling in multiple systems. Plexins were originally characterized for their role modulating cytoskeletal activity to regulate axon guidance during nervous system development. Thereafter, different semaphorin-plexin complexes were identified in the nervous system that have diverse functions in neurons, astrocytes, glia, oligodendrocytes, and brain derived-tumor cells, providing unexpected but meaningful insights into the biological activities of this protein family. Here, we review the overall structure and relevant downstream signaling cascades of plexins. We consider the current knowledge regarding the function of semaphorin-plexin cascades in the nervous system, including the most recent data regarding their roles in neuronal development, neuroinflammation, and glioma.
Autor/es principal/es: Dai, Lu
Shen, Kai-Feng
Zhang, Chun-Qing
URI: http://hdl.handle.net/10201/135731
DOI: https://doi.org/10.14670/HH-18-625
Tipo de documento: info:eu-repo/semantics/article
Número páginas / Extensión: 10
Derechos: info:eu-repo/semantics/openAccess
Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Aparece en las colecciones:Vol.38,nº11 (2023)

Ficheros en este ítem:
Fichero Descripción TamañoFormato 
a7711c99-5d18-4734-a17c-d63eaa394dfc(2).pdf2,53 MBAdobe PDFVista previa
Visualizar/Abrir


Este ítem está sujeto a una licencia Creative Commons Licencia Creative Commons Creative Commons