A Review of Cerebrospinal Fluid Circulation and the Pathogenesis of Congenital Hydrocephalus

被引:0
作者
Mingzhao Zhang
Xiangjun Hu
Lifeng Wang
机构
[1] Beijing Institute of Radiation Medicine,Laboratory of pathology
来源
Neurochemical Research | 2024年 / 49卷
关键词
Cerebrospinal fluid circulation; Choroid plexus; Congenital hydrocephalus; Cilia; Aqueductal stenosis;
D O I
暂无
中图分类号
学科分类号
摘要
The brain’s ventricles are filled with a colorless fluid known as cerebrospinal fluid (CSF). When there is an excessive accumulation of CSF in the ventricles, it can result in high intracranial pressure, ventricular enlargement, and compression of the surrounding brain tissue, leading to potential damage. This condition is referred to as hydrocephalus. Hydrocephalus is classified into two categories: congenital and acquired. Congenital hydrocephalus (CH) poses significant challenges for affected children and their families, particularly in resource-poor countries. Recognizing the psychological and economic impacts is crucial for developing interventions and support systems that can help alleviate the distress and burden faced by these families. As our understanding of CSF production and circulation improves, we are gaining clearer insights into the causes of CH. In this article, we will summarize the current knowledge regarding CSF circulation pathways and the underlying causes of CH. The main causes of CH include abnormalities in the FoxJ1 pathway of ventricular cilia, dysfunctions in the choroid plexus transporter Na+-K+-2Cl- contransporter isoform 1, developmental abnormalities in the cerebral cortex, and structural abnormalities within the brain. Understanding the causes of CH is indeed crucial for advancing research and developing effective treatment strategies. In this review, we will summarize the findings from existing studies on the causes of CH and propose potential research directions to further our understanding of this condition.
引用
收藏
页码:1123 / 1136
页数:13
相关论文
共 242 条
[51]  
Dewan A(2012)A ciliopathy with hydrocephalus, isolated craniosynostosis, hypertelorism, and clefting caused by deletion of Kif3a[J] Semin Fetal Neonatal Med 17 285-398
[52]  
Rattani R(2020)Dysfunctional cilia lead to altered ependyma and choroid plexus function, and result in the formation of hydrocephalus[J] Nat Med 26 1754-1
[53]  
Mekary RT(2014)Loss of Rsph9 causes neonatal hydrocephalus with abnormal development of motile cilia in mice[J] Reprod Toxicol 48 88-251
[54]  
Muir S(2005)Nonsense mutation in CFAP43 causes normal-pressure hydrocephalus with ciliary abnormalities[J] Development 132 5329-52
[55]  
Wang BC(2020)CFAP43 modulates ciliary beating in mouse and Xenopus[J] Sci Rep 10 12435-285
[56]  
Warf I(2019)Rethinking the cilia hypothesis of hydrocephalus[J] Neurology 92 e2364-448
[57]  
Bachy R(2020)Breaking the barrier: Invitro models to study choroid plexus development[J] Dev Biol 459 109-634
[58]  
Kozyraki M(2022)NLRP3 inflammasome-mediated choroid plexus hypersecretion contributes to hydrocephalus after intraventricular hemorrhage via phosphorylated NKCC1 channels[J] Neurobiol Dis 175 105913-126
[59]  
Wassef J(2021)Choroid plexus NKCC1 mediates cerebrospinal fluid clearance during mouse early postnatal development[J] Curr Opin Cell Biol 73 41-79
[60]  
Buddensiek A(2022)TRPV4 antagonists: a patent review (2015–2020)[J] J Neuroinflammation 19 163-95