The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy

Fyn is a cytoplasmic tyrosine kinase (TK) that is a nonreceptor and a member of the Src family of kinases (SFKs). It is involved in several transduction pathways in the central nervous system (CNS), such as oligodendrocyte development, myelination, axon guidance, and synaptic transmission. Owing to...

Full description

Saved in:
Bibliographic Details
Main Authors: Jiao Zhou, Xiang Lu, Haichuan Wang
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-11-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2024.1476856/full
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846151926812508160
author Jiao Zhou
Jiao Zhou
Xiang Lu
Haichuan Wang
author_facet Jiao Zhou
Jiao Zhou
Xiang Lu
Haichuan Wang
author_sort Jiao Zhou
collection DOAJ
description Fyn is a cytoplasmic tyrosine kinase (TK) that is a nonreceptor and a member of the Src family of kinases (SFKs). It is involved in several transduction pathways in the central nervous system (CNS), such as oligodendrocyte development, myelination, axon guidance, and synaptic transmission. Owing to its wide range of activities in the molecular signaling pathways that underpin both neuropathologic and neurodevelopmental events, Fyn has remained of great interest for more than a century. Accumulating preclinical data have highlighted the potential role of Fyn in the pathophysiology of neonatal hypoxic-ischaemic encephalopathy (HIE). By mediating important signaling pathways, Fyn may control glutamate excitotoxicity, promote neuroinflammation and facilitate the death of neurons caused by oxidative stress. In this review, we address new evidence regarding the role of Fyn in the pathogenesis of this condition, with the aim of providing a reference for the development of new strategies to improve the prognosis of neonatal HIE. In addition, we also offer insights into additional Fyn-related molecular mechanisms involved in HIE pathology.
format Article
id doaj-art-ad08525fae814b4681c6f5c7f90d6ec0
institution Kabale University
issn 1662-5102
language English
publishDate 2024-11-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Cellular Neuroscience
spelling doaj-art-ad08525fae814b4681c6f5c7f90d6ec02024-11-27T04:21:21ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022024-11-011810.3389/fncel.2024.14768561476856The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathyJiao Zhou0Jiao Zhou1Xiang Lu2Haichuan Wang3Department of Reproductive Medicine Nursing, West China Second University Hospital, Sichuan University, Chengdu, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children (Sichuan University), Ministry of Education, Chengdu, ChinaDepartment of Cardiology, The First People’s Hospital of Yuexi County, Yuexi, ChinaDepartment of Paediatrics, Sichuan Academy of Medical Science and Sichuan Provincial People’s Hospital, School of Medicine, University of Electronic Science and Technology of China, Chengdu, ChinaFyn is a cytoplasmic tyrosine kinase (TK) that is a nonreceptor and a member of the Src family of kinases (SFKs). It is involved in several transduction pathways in the central nervous system (CNS), such as oligodendrocyte development, myelination, axon guidance, and synaptic transmission. Owing to its wide range of activities in the molecular signaling pathways that underpin both neuropathologic and neurodevelopmental events, Fyn has remained of great interest for more than a century. Accumulating preclinical data have highlighted the potential role of Fyn in the pathophysiology of neonatal hypoxic-ischaemic encephalopathy (HIE). By mediating important signaling pathways, Fyn may control glutamate excitotoxicity, promote neuroinflammation and facilitate the death of neurons caused by oxidative stress. In this review, we address new evidence regarding the role of Fyn in the pathogenesis of this condition, with the aim of providing a reference for the development of new strategies to improve the prognosis of neonatal HIE. In addition, we also offer insights into additional Fyn-related molecular mechanisms involved in HIE pathology.https://www.frontiersin.org/articles/10.3389/fncel.2024.1476856/fullFynHIEmolecular mechanismpathogenesisbrain
spellingShingle Jiao Zhou
Jiao Zhou
Xiang Lu
Haichuan Wang
The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
Frontiers in Cellular Neuroscience
Fyn
HIE
molecular mechanism
pathogenesis
brain
title The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
title_full The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
title_fullStr The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
title_full_unstemmed The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
title_short The underlying molecular mechanisms of Fyn in neonatal hypoxic-ischaemic encephalopathy
title_sort underlying molecular mechanisms of fyn in neonatal hypoxic ischaemic encephalopathy
topic Fyn
HIE
molecular mechanism
pathogenesis
brain
url https://www.frontiersin.org/articles/10.3389/fncel.2024.1476856/full
work_keys_str_mv AT jiaozhou theunderlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT jiaozhou theunderlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT xianglu theunderlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT haichuanwang theunderlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT jiaozhou underlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT jiaozhou underlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT xianglu underlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy
AT haichuanwang underlyingmolecularmechanismsoffyninneonatalhypoxicischaemicencephalopathy