The functional and molecular roles of p75 neurotrophin receptor (p75 NTR ) in epilepsy

Abstract

Epilepsy is a chronic neurological disorder manifested by recurring unprovoked seizures resulting from an imbalance in the inhibitory and excitatory neurotransmitters in the brain. The process of epileptogenesis involves a complex interplay between the reduction of inhibitory gamma-aminobutyric acid (GABA) and the enhancement of excitatory glutamate. Pro-BDNF/p75^NTR expression is augmented in both glial cells and neurons following epileptic seizures and status epileptics (SE). Over-expression of p75^NTR is linked with the pathogenesis of epilepsy, and augmentation of pro-BDNF/p75^NTR is implicated in the pathogenesis of epilepsy. However, the precise mechanistic function of p75^NTR in epilepsy has not been completely elucidated. Therefore, this review aimed to revise the mechanistic pathway of p75^NTR in epilepsy.

Plain Language Summary

Roles of p75 neurotrophin receptor (p75NTR) in epilepsy: Epilepsy is a chronic neurological disorder manifested by recurring unprovoked seizures resulting from an imbalance in the inhibitory and excitatory neurotransmitters in the brain. The process of epileptogenesis involves a complex interplay between the reduction of inhibitory gamma-aminobutyric acid (GABA) and the enhancement of excitatory glutamate. Pro-BDNF/p75NTR expression is augmented in both glial cells and neurons following epileptic seizures and status epileptics (SE). Over-expression of p75NTR is linked with the pathogenesis of epilepsy, and augmentation of pro-BDNF/p75NTR is implicated in the pathogenesis of epilepsy. However, the precise mechanistic function of p75NTR in epilepsy has not been completely elucidated.

Keywords

Epilepsy

Introduction

The p75 neurotrophin receptor (p75^NTR) was initially identified in 1973 as a low-affinity nerve growth factor receptor (LNGFR).¹ The p75^NTR is considered to be a functional receptor for various growth factors, such as pro-brain derived neurotrophic factor (pro-BDNF), neurotrophin 3 (NT-3), and neurotrophin 4 (NT-4).² Noteworthy, p75^NTR is a member of the superfamily of tumor necrosis factor receptors.³ It consists of 3 domains, intracellular, transmembrane and extracellular.² The tendency of p75^NTR is toward dimerization rather than trimerization, owing to the activation of the tyrosine kinase co-receptor.⁴ The p75^NTR promotes neuronal maturation, differentiation, and survival.⁴ The induction of apoptosis by neurotrophins through p75^NTR involves the activation of p53, caspase, and c-Jun N-terminal kinase signaling.⁵ The engagement of neurotrophins with p75^NTR enhances the viability of neurons through the initiation of the nuclear factor kappa B (NF-κB) signaling pathway.⁶ p75^NTR also involves in interactions with various receptors, such as interaction with the sortilin receptor, which serves as a co-receptor-for-the-functional effects of multiple neurotrophins, including BDNF.⁷ Additionally, the pro-BDNF exhibits a more specific binding affinity towards p75^NTR in the presence of sortilin receptors.⁸ Moreover, the interaction between p75^NTR and tropomyosin receptor kinase A (TrkA), resulted in the reduction of p75^NTR-induced apoptosis.⁹ Also, p75^NTR with the help of the nogo-66 receptor (NgR1) induces apoptosis and inhibits neuronal myelin sheath.¹⁰ The effects of diverse signaling pathways, such as NF-κB, which plays a crucial role in the advancement and progression of neurodegenerative disorders, are mediated by p75^NTR ¹¹ (Figure 1).

Figure 1.

Pathway of p75^NTR.

It has been shown that p75^NTR is highly expressed during neuronal development, though these receptors are re-expressed in different pathological conditions including neurodegenerative diseases and epilepsy. For example, toxic peptides and proteins like amyloid beta (Aβ) which accumulated in AD are regarded as a ligand for p75^NTR that induces axonal degeneration and synaptic dysfunction.¹² It has been demonstrated that the signaling of p75^NTR plays a role in epilepsy, though the precise mechanism was not fully elucidated. Thus, this review tries to show how p75^NTR signaling is intricate in epilepsy neuropathology.

Role of p75^NTR in epilepsy

Epilepsy is a chronic neurological disorder manifested by recurring unprovoked seizures resulting from an imbalance in the inhibitory and excitatory neurotransmitters in the brain.¹³ Epilepsy is classified as a primary (idiopathic) epilepsy when the underlying causes are unidentified.¹⁴ However, secondary (symptomatic) epilepsy is caused by different neurological disorders such as brain injury, brain tumors, neurodegenerative diseases, and infection. Epilepsy is regarded as the fourth common neurological disease affecting more than 50 million in the world. The incidence of epilepsy is 2%–5% in the general population.^15,16 Notably, many signaling pathways are implicated in the pathogenesis of epileptogenesis and epilepsy.¹⁶

It has been reported that pro-BDNF and mature BDNF (mBDNF) induce divergent physiological responses by activating p75^NTR and TrkB respectively.¹⁷ Of note, pro-BDNF/p75^NTR is essential for cognitive function, and impairment of this signaling is associated with the development of neurodegenerative and neurodevelopmental disorders.¹⁸ Neuronal cell death in the hippocampus following status epilepticus (SE) is mainly mediated by pro-BDNF/p75^NTR signaling since administration of antibodies against pro-BDNF prevents hippocampal cell death following pilocarpine-induced SE.¹⁹ Of interest, proBDNF is localized to mossy fibers and microglia following SE. in addition, p75^NTR is momentarily induced primarily in axons and axon terminals following SE, as well as in neuron and astrocyte cell bodies. Furthermore, proBDNF and p75^NTR increased independently of cell death and their localization was different depending on the severity of SE. The expression of pro neurotrophin co-receptors, sortilin and sorCS2. Following severe SE, sorCS2, but not sortilin, was elevated in neurons and astrocytes.²⁰ These data indicate that important differences exist between rat and mouse in the pro-neurotrophin response following SE. Moreover, the proBDNF and p75^NTR increase after seizures in the absence of significant cell death suggesting that proneurotrophin signaling may play other roles following SE. However, Pro-BDNF/p75^NTR expression is augmented in both glial cells and neurons following seizure and SE in mice regardless of neuronal cell death.²⁰ This finding signifies that pro-BDNF/p75^NTR is linked with epileptogenesis by inhibiting GABA neurotransmission.²⁰ It has been observed that pro-BDNF/p75^NTR signaling inhibits GABA_A receptor and synaptic plasticity though BDNF/TrkB signaling activates GABA long-term potentiation.^21,22 In addition, pro-BDNF/p75^NTR via the Rho-ROCK pathway increases the internalization of the GABA_A receptor and induces degradation of these receptors by the lysosomes leading to disruption of GABAergic neurotransmission in the cortical neurons.²³ In SE, cleavage of BDNF to mBDNF by plasminogen and plasminogen activator is impaired leading to increased pro-BDNF which via the activation of p75^NTR induces recurrent seizure by inhibiting GABAergic neurotransmission.^24,25 Mutation of the plasminogen gene in mice results in recurrent seizure and SE.²⁶ Therefore, a deficiency of plasminogen induces severe epilepsy through augmentation of augmentation of pro-BDNF/p75^NTR.²⁶ Consequently, dysregulation of neuronal plasminogen is involved in the pathogenesis of epilepsy.²⁷ However, many studies confirmed that neuronal plasminogen has little or no role in the pathogenesis of epilepsy.^28,29 Experimental and clinical studies showed that endogenous tissue plasminogen activator (t-PA) was increased following stroke but not intricate in the pathogenesis of epileptogenesis.²⁸ Likewise, in animal model epilepsy, t-PA plays a little role in the pathogenesis of epileptogenesis.²⁹ Thus, t-PA is not involved in the pathogenesis of post-stroke epilepsy.

Furthermore, KCC2 which regulates GABAergic neurotransmission and balance between inhibitory/excitatory neural circuits, inhibits epileptogenesis. Down-regulation of KCC2 leads to epileptogenesis in both preclinical and clinical studies.^30,31 Neurons from patients with temporal lobe epilepsy (TLE) had low expression of KCC2.³⁰ Interestingly, down-regulation of KCC2 following SE persists for weeks leading to the reduction of inhibitory GABAergic neurotransmission and induction of excitatory neurotransmission with subsequent recurrent seizures.³¹ Of note, pro-BDNF/p75^NTR inhibits the expression of neuronal KCC2 in the TLE animal model.³² However, BDNF/TrkB promotes the expression of KCC2 in the GABAergic neurons.³³ Indeed, pro-BDNF triggers the expression of p75^NTR,²³ leading to epileptogenesis by inhibiting GABAergic neurotransmission. Notoriously, GABA-mediated depolarization provokes the expression of p75^NTR.³⁴ These findings illustrated that pro-BDNF/p75^NTR is involved in the pathogenesis of epilepsy. Conversely, inhibition of p75^NTR before or at the onset of SE did not prevent subsequent seizures in pilocarpine-induced SE in mice.³⁵ In addition, p75^NTR null mice experience higher excitability in the cortical neurons.³⁶ Thus, pro-BDNF/p75^NTR signaling seems to have a neuroprotective against epileptogenesis.³⁶ A postmortem study involved 18 hippocampal specimens from patients with TLE showed that p75^NTR expression was increased in hippocampal neurons contributing to epileptogenesis and neuronal cell deaths.³⁷ Furthermore, the increased expression of p75^NTR in hippocampal neurons of TLE may critically influence neuronal survival during the epileptogenic process.³⁸ These observations suggest that over-expression of p75^NTR is linked with the pathogenesis of severe epilepsy and TLE and SE (Figure 2). However, the mechanistic role of p75^NTR and related ligands in epilepsy is not fully elucidated.

Figure 2.

Role of p75^NTR in epilepsy.

Mechanistic pathways of p75^NTR in epilepsy

PI3K/Aκt

It has been shown that phosphoinositide 3 kinase (PI3K) and protein kinase B also known as the Aκt signaling pathway regulate several neurological processes that are critical for the development of the central nervous system, including neurogenesis, synaptic plasticity, neuronal differentiation, and autophagy.³⁹ Exaggerated PI3K/Aκt is linked with hippocampal neuronal injury in rat epilepsy model, and inhibition of this pathway prevents hippocampal neurodegeneration.⁴⁰ Upregulation of neuronal PI3K is linked with epileptogenesis and induction of epilepsy.⁴¹ Therefore, PI3K inhibitor LY294002 prevents pentylenetetrazole (PTZ)-induced epileptic seizure in zebrafish model.⁴¹ Besides, the Aκt signaling pathway promotes epileptic seizure by enhancing the expression of the mechanistic target of rapamycin (mTOR) in the rat TLE model.⁴² In this state, Aκt inhibitor perifosine attenuates kainic acid (KA)-induced TLE in rats.⁴² It has been shown that the PI3K/Aκt signaling pathway promotes mTOR-induced epileptogenesis in hippocampal cultured neurons of the post-traumatic epilepsy model.⁴³ Interestingly, a dual inhibitor of mTOR and PI3K NVP-BEZ235 attenuates the development and progression of epileptic seizures.⁴³

On the other hand, p75^NTR activation is linked with stimulation of the PI3K/Aκt/mTOR signaling pathway. It has been reported that p75^NTR signaling increases the activation of the PI3K/Aκt signaling pathway.⁴⁴ Remarkably, pro-BDNF/p75^NTR regulates the excitability of cortical neurons by modulating the PI3K/Aκt signaling pathway.³⁶ However, the preclinical study demonstrated that p75^NTR activates autophagy by inhibiting the PI3K/Aκt/mTOR signaling pathway.⁴⁵ Of note, over-expression of p75^NTR during aging promotes the expression of mTOR-mediated synaptic dysfunction in mice.⁴⁶ In addition, mTOR inhibitor rapamycine promotes autophagy through a p75^NTR-dependent pathway.⁴⁷ Different studies confirmed that mTOR signaling is highly upregulated in epilepsy.^48,49 It has been observed that the BDNF/p75^NTR axis promotes hippocampal glutamatergic excitotoxicity by enhancing the mTOR signaling pathway.⁵⁰

Likewise, The PI3K/Aκt/mTOR signaling pathway is modulated by p75^NTR-mediated enhancement of phosphatase and tensin homolog (PTEN) expression.⁴⁷ Of note, PTEN overexpression is associated with glutamate excitotoxicity, neuronal cell death, and epileptogenesis.⁵¹ An experimental study revealed that the administration of PTEN inhibitor picolinate attenuates KA-induced TLE in mice.⁵¹ Interestingly, PTEN variants are associated with drug resistance in patients with focal epilepsy.⁵²

Therefore, p75^NTR activation is implicated in epileptogenesis by increasing PTEN expression and dysregulation of the PI3K/Aκt/mTOR signaling pathway (Figure 3).

Figure 3.

p75NTR activation and epileptogenesis.

Caspase 3 and p75^NTR

Cysteine proteases, or caspases, play a key role in apoptosis. Caspases are produced as dormant proenzymes and can be classified as effectors (caspase 3, 6, 7), or initiators (caspase 2, 8, 9, 10). The primary mediator of neuronal apoptosis is caspase 3, which also performs non-apoptotic tasks. The physiological functions of caspases are control memory and synaptic functions.⁵³ The p75^NTR activates caspase 3 leading to progressive neuronal injury.⁵⁴ Song and coworkers⁵⁵ found that PTEN is necessary for shifting the switch between apoptotic and survival pathways in rat brain neurons. Regardless of whether TrkB is activated by BDNF or not, apoptosis is triggered instantly by pro-BDNF and p75^NTR. The inhibition of PTEN blocks the apoptotic pathway and augments the BDNF/TrkB signaling pathway. This evidence is corroborated by the confirmation that inhibiting PTEN decreases p75^NTR-mediated neuronal damage and cell death in rats with pilocarpine-induced epilepsy.⁵⁵

Caspase 3 is extremely activated in patients with TLE⁵⁶ signifying that caspase 3 is involved in epileptogenesis, and inhibition of this pathway could be a novel pathway in the management of epilepsy. A previous study indicated that over-expression of caspase 3 is present in resected neocortex from patients with TLE.^57,58 Thus, targeting of caspase 3 may be effective against epileptogenesis. Besides, caspase 3 inhibitors attenuate neuronal loss in traumatic brain injury which is intricate in the development of epilepsy.⁵⁹ Different studies reported that pharmacological suppression of caspase 3 was effective in TLE.⁶⁰ In this state, pro-BDNF/p75^NTR through activation of caspase 3 may lead to neuronal injury, apoptosis, and induction of epileptogenesis.⁶¹ Therefore, direct inhibition of the pro-BDNF/p75^NTR signaling pathway or indirect suppression of caspase 3 could be an effective therapeutic strategy in epilepsy (Figure 4).

Figure 4.

Caspase 3 and p75NTR in epileptogenesis.

NF-κB and p75^NTR

NF-κB, a collective of transcription factors, plays a crucial role in diverse physiological and pathological processes.⁶² Two principal pathways of NF-κB have been described, namely the canonical and non-canonical pathways. The canonical NF-κB pathway is initiated in reaction to various external stimuli involved in immune response, inflammation, cell proliferation, and survival.⁶³ This pathway results in the rapid release of NF-κB and the subsequent inhibition of IκB, which triggers IκB kinase.⁶⁴ Higher levels of NF-κB expression trigger the expression of negative regulators like IκBα, which limit the conical NF-κB pathway.⁶² However, tumor necrosis factor-alpha (TNF-α) stimulates the non-conical NF-κB pathway by activating NF-κB inducing kinase (NIK).⁶³ The non-conical NF-κB pathway plays a complex role in the thymus’s T cell maturation and immune response regulation.⁶⁴ Moreover, an in vitro study found that p75^NTR activates NF-κB during the apoptosis pathway.⁶⁵ It’s interesting to note that p75^NTR causes cognitive impairment in an animal model study by triggering NF-κB.⁶ Furthermore, NF-κB is intricate in the epileptogenesis process by increasing the expression of genes involved in the release of pro-inflammatory cytokines, chemokines, and the development of inflammation.⁶⁶ NF-κB is highly expressed in glial cells and neurons, and upregulated of NF-κB is associated with BBB dysfunction and GABA inhibition.⁶⁶ NF-κB is highly upregulated in neurons and astrocytes following epileptic seizure within 4 hr in animal epilepsy models.⁶⁷ Wang et al.⁶⁸ observed that neuronal expression of NF-κB following SE persist for 14 days. Pro-inflammatory cytokines which released from astrocytes and glial cells during epileptic seizure promote the expression of NF-κB and induction of further recurrent epileptic seizure.⁶⁹ Therefore, p75^NTR via activation of NF-κB may induce the development and progression of epilepsy (Figure 5).

Figure 5.

NF-κB and p75^NTR in epileptogenesis.

Ras homology family member A/Rho/ROCK and p75^NTR

RhoA, a member of the Ras homology family, is a small GPTase that plays various cellular roles. It is extensively expressed in neurons and in glial cells.⁷⁰ RhoA overexpression is linked to the onset and progression of neurodegenerative diseases.⁷¹ It has been shown that pro-BDNF-induced p75^NTR activation increases RhoA signaling and the expression of apoptosis-mediated proteins like synaptophysin, which causes neuronal apoptosis.⁷⁰ Additionally, the p75^NTR/RhoA signaling pathway is triggered in response to isoflurane, which causes neurotoxicity.⁷² Moreover, fingolimod enhances the synaptic plasticity of the hippocampus by suppressing the expression of p75^NTR and lowering RhoA signaling in the Huntington disease (HD) mouse model.⁷³ Identical to Ras, Rho is balanced by regulatory proteins such as GTPase activating protein. ROCK which is also known as Rho kinase is a serine/threonine protein kinase with a molecular weight of 160 kDa. Two types of ROCK are present, ROCK1 which is expressed in non-neuronal tissues and ROCK2 is mainly expressed in neuronal tissues including the brain and spinal cord.⁷⁴ Rho-ROCK signaling pathway is implicated in different pathophysiological processes, for example, it inhibits axonal growth during brain injury, and Rho-ROCK inhibitors can improve axonal growth.⁷⁵ In addition, over-expression of the Rho-ROCK signaling pathway is associated with the development of Alzheimer’s disease (AD).⁷⁶ Rho-ROCK is highly expressed in neurons and astrocytes that are intricate in synaptic plasticity.⁷⁷ Expression of the Rho-ROCK signaling pathway in the hippocampus is augmented following KA-induced SE.⁷⁸ It has been shown that Rho-ROCK inhibitor fasudil attenuates KA-induced neuronal injury.⁷⁹ Likewise, Rho-ROCK inhibitor Y-27632 decreased the expression of ROCK2 in experimental epileptic seizure in mice.⁸⁰ Different studies revealed that p75^NTR signaling pathways activate neuronal expression of Rho-ROCK and linked neuronal injury.^81-83 These findings that p75^NTR signaling pathway via activation of RhoA and Rho-ROCK signaling increases the risk of epileptic seizure (Figure 6).

Figure 6.

Rho/ROCK and p75^NTR in epileptogenesis.

Taken together, p75^NTR signaling pathway is implicated in epileptogenesis and the pathogenesis of epilepsy by inducing various molecular pathways. Targeting of p75^NTR signaling pathway could be a novel pathway in the management of epilepsy.

Conclusions

Epilepsy is a chronic neurological disorder manifested by recurring seizures resulting from an imbalance in the inhibitory and excitatory neurotransmitters in the brain. Many signaling pathways are implicated in the pathogenesis of epileptogenesis and epilepsy. It has been observed that p75^NTR a function receptor of proBDNF is dysregulated in epilepsy and implicated in the development and progression of SE and TLE. However, the mechanistic role of p75^NTR in the pathogenesis of epilepsy is not completely clarified. Therefore, this review was suggested to review the mechanistic pathway of p75^NTR in epilepsy. Interestingly, p75^NTR activation is implicated in epileptogenesis by increasing the expression of different signaling pathways. For example, p75^NTR increases PTEN expression and dysregulation of the PI3K/Aκt/mTOR signaling pathway that induces epileptogenesis and the induction of epileptic seizure. As well, p75^NTR enhances the activity of caspase 3 with subsequent progressive neuronal injury and epileptogenesis. In addition, p75^NTR promotes the expression of NF-κB, RhoA and Rho-ROCK signaling which induces the progression of epileptic seizure and the development of TLE. Taken together, the p75^NTR signaling pathway is associated with epileptogenesis and the pathogenesis of epilepsy by inducing various molecular pathways. Hence, targeting of p75^NTR signaling pathway and associated pathways could be an innovative therapeutic strategy in the management of epilepsy. This review suggests doing preclinical and clinical studies to confirm this scientific claim.

Footnotes

Author contributions

AT, HMA-K, AIA and AkA conceptualized the manuscript, wrote, edited and reviewed the main text and approved the final edition of the manuscript. OE, AAF, FA, HMS and GE-SB prepared the figures, wrote, corrected, amended and approved the final edition of the manuscript.

Declaration of conflicting interests

The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Funding

The author(s) received no financial support for the research, authorship, and/or publication of this article.

ORCID iD

Hebatallah M. Saad

Data availability statement

Data sharing is not applicable to this article as no new data were created or analyzed in this study.*

References

Underwood

Coulson

. The p75 neurotrophin receptor. Int J Biochem Cell Biol. 2008;40:1664-1668.

Ismail

Leong

AMFI

Hami

, et al. A narrative review of brain-derived neurotrophic factor (BDNF) on cognitive performance in Alzheimer’s disease. Growth Factors. 2020;38:210-225.

Kuhn

Edamura

Bhatia

, et al. Molecular dissection of TNFR-TNFα bidirectional signaling reveals both cooperative and antagonistic interactions with p75 neurotrophic factor receptor in axon patterning. Mol Cell Neurosci. 2020;103:103467.

Goncharuk

Artemieva

Nadezhdin

, et al. Revising the mechanism of p75NTR activation: intrinsically monomeric state of death domains invokes the “helper” hypothesis. Sci Rep. 2020;10:13686.

Sankorrakul

Qian

Thangnipon

, et al.

Is there a role for the p75 neurotrophin receptor in mediating degeneration during oxidative stress and after hypoxia?

J Neurochem. 2021;158:1292-1306.

Wei

Yang

Feng

, et al. p75NTR enhances cognitive dysfunction in a mouse Alzheimer’s disease model by inhibiting microRNA-210-3p-mediated PCYT2 through activation of NF-κB. Int J Biol Macromol. 2023;225:404-415.

Eggert

Kins

Endres

, et al. Brothers in arms: proBDNF/BDNF and sAPPα/Aβ-signaling and their common interplay with ADAM10, TrkB, p75NTR, sortilin, and sorLA in the progression of Alzheimer’s disease. Biol Chem. 2022;403:43-71.

Riolo

Ricci

De Angelis

, et al. BDNF and pro-BDNF in amyotrophic lateral sclerosis: a new perspective for biomarkers of neurodegeneration. Brain Sci. 2022;12:617.

Blondy

Christou

David

, et al. Neurotrophins and their involvement in digestive cancers. Cell Death Dis. 2019;10:123.

10.

Dave

Shah

, et al. Unveiling the modulation of Nogo receptor in neuroregeneration and plasticity: novel aspects and future horizon in a new frontier. Biochem Pharmacol. 2023;210:115461.

11.

Zhang

Kisiswa

Ramanujan

, et al. Structural basis of NF-κB signaling by the p75 neurotrophin receptor interaction with adaptor protein TRADD through their respective death domains. J Biol Chem. 2021;297:100916.

12.

Dechant

Barde

Y-A

. The neurotrophin receptor p75NTR: novel functions and implications for diseases of the nervous system. Nat Neurosci. 2002;5:1131-1136.

13.

AlRuwaili

Al-Kuraishy

Al-Gareeb

, et al. The possible role of brain-derived neurotrophic factor in epilepsy. Neurochem Res. 2023;49:533-547.

14.

Alnaaim

Al-kuraishy

Al-Gareeb

, et al. New insights on the potential anti-epileptic effect of metformin: mechanistic pathway. J Cell Mol Med. 2023;27:3953-3965.

15.

Al-Kuraishy

Al-Gareeb

Rauf

, et al. Mechanistic insight and possible mechanism of seizure in Covid-19: the nuances and focal points. CNS Neurol Disord Drug Targets. 2022;22:875-883.

16.

Beghi

. The epidemiology of epilepsy. Neuroepidemiology. 2020;54:185-191.

17.

Pang

Woo

. The yin and yang of neurotrophin action. Nat Rev Neurosci. 2005;6:603-614.

18.

Garcia

Nicolini

, et al. Altered balance of proteolytic isoforms of pro-brain-derived neurotrophic factor in autism. J Neuropathol Exp Neurol. 2012;71:289-297.

19.

Volosin

Trotter

Cragnolini

, et al. Induction of proneurotrophins and activation of p75NTR-mediated apoptosis via neurotrophin receptor-interacting factor in hippocampal neurons after seizures. J Neurosci. 2008;28:9870-9879.

20.

VonDran

LaFrancois

Padow

, et al. p75NTR, but not proNGF, is upregulated following status epilepticus in mice. ASN Neuro. 2014;6:1759091414552185.

21.

Langlois

Diabira

Ferrand

, et al. NMDA-dependent switch of proBDNF actions on developing GABAergic synapses. Cereb Cortex. 2013;23:1085-1096.

22.

Gubellini

Ben-Ari

Gaïarsa

J-L

. Endogenous neurotrophins are required for the induction of GABAergic long-term potentiation in the neonatal rat hippocampus. J Neurosci. 2005;25:5796-5802.

23.

Riffault

Medina

Dumon

, et al. Pro-brain-derived neurotrophic factor inhibits GABAergic neurotransmission by activating endocytosis and repression of GABAA receptors. J Neurosci. 2014;34:13516-13534.

24.

Porcher

Medina

Gaiarsa

J-L

. Mechanism of BDNF modulation in GABAergic synaptic transmission in healthy and disease brains. Front Cell Neurosci. 2018;12:273.

25.

Angelucci

Čechová

Průša

, et al. Amyloid beta soluble forms and plasminogen activation system in Alzheimer’s disease: consequences on extracellular maturation of brain-derived neurotrophic factor and therapeutic implications. CNS Neurosci Ther. 2019;25:303-313.

26.

Ndode-Ekane

Pitkänen

. Urokinase-type plasminogen activator receptor modulates epileptogenesis in mouse model of temporal lobe epilepsy. Mol Neurobiol. 2013;47:914-937.

27.

Shmakova

Rubina

Anokhin

, et al. The role of plasminogen activator system in the pathogenesis of epilepsy. Biochemistry (Moscow). 2019;84:979-991.

28.

Tan

Pandher

, et al. Tissue plasminogen activator does not alter development of acquired epilepsy. Epilepsia. 2012;53:1998-2004.

29.

Rantala

Kemppainen

Ndode-Ekane

, et al. Urokinase-type plasminogen activator deficiency has little effect on seizure susceptibility and acquired epilepsy phenotype but reduces spontaneous exploration in mice. Epilepsy Behav. 2015;42:117-128.

30.

Pathak

Weissinger

Terunuma

, et al. Disrupted dentate granule cell chloride regulation enhances synaptic excitability during development of temporal lobe epilepsy. J Neurosci. 2007;27:14012-14022.

31.

Huberfeld

Wittner

Clemenceau

, et al. Perturbed chloride homeostasis and GABAergic signaling in human temporal lobe epilepsy. J Neurosci. 2007;27:9866-9873.

32.

Riffault

Kourdougli

Dumon

, et al. Pro-brain-derived neurotrophic factor (proBDNF)-mediated p75NTR activation promotes depolarizing actions of GABA and increases susceptibility to epileptic seizures. Cereb Cortex. 2018;28:510-527.

33.

Ludwig

Uvarov

Soni

, et al. Early growth response 4 mediates BDNF induction of potassium chloride cotransporter 2 transcription. J Neurosci. 2011;31:644-649.

34.

Shulga

Magalhaes

Autio

, et al. The loop diuretic bumetanide blocks posttraumatic p75NTR upregulation and rescues injured neurons. J Neurosci. 2012;32:1757-1770.

35.

Grabenstatter

Carlsen

Raol

, et al. Acute administration of the small-molecule p75NTR ligand does not prevent hippocampal neuron loss or development of spontaneous seizures after pilocarpine-induced status epilepticus. J Neurosci Res. 2014;92:1307-1318.

36.

Gibon

Buckley

Unsain

, et al. proBDNF and p75NTR control excitability and persistent firing of cortical pyramidal neurons. J Neurosci. 2015;35:9741-9753.

37.

Özbas-Gerçeker

Gorter

Redeker

, et al. Neurotrophin receptor immunoreactivity in the hippocampus of patients with mesial temporal lobe epilepsy. Neuropathol Appl Neurobiol. 2004;30:651-664.

38.

Fernández-García

Sancho-Balsells

Longueville

, et al. Astrocytic BDNF and TrkB regulate severity and neuronal activity in mouse models of temporal lobe epilepsy. Cell Death Dis. 2020;11:411.

39.

Long

H-Z

Cheng

Zhou

Z-W

, et al. PI3K/AKT signal pathway: a target of natural products in the prevention and treatment of Alzheimer’s disease and Parkinson’s disease. Front Pharmacol. 2021;12:648636.

40.

. Down-regulation of long noncoding RNA MALAT1 protects hippocampal neurons against excessive autophagy and apoptosis via the PI3K/Akt signaling pathway in rats with epilepsy. J Mol Neurosci. 2018;65:234-245.

41.

Mazumder

Kumari

Singh

. Anticonvulsant action of a selective phosphatidylinositol-3-kinase inhibitor LY294002 in pentylenetetrazole-mediated convulsions in zebrafish. Epilepsy Res. 2019;157:106207.

42.

Zhu

Kai

Chen

, et al. Akt inhibitor perifosine prevents epileptogenesis in a rat model of temporal lobe epilepsy. Neurosci Bull. 2018;34:283-290.

43.

Berdichevsky

Dryer

Saponjian

, et al. PI3K-Akt signaling activates mTOR-mediated epileptogenesis in organotypic hippocampal culture model of post-traumatic epilepsy. J Neurosci. 2013;33:9056-9067.

44.

Roux

Bhakar

Kennedy

, et al. The p75 neurotrophin receptor activates Akt (protein kinase B) through a phosphatidylinositol 3-kinase-dependent pathway. J Biol Chem. 2001;276:23097-23104.

45.

Shi

Bian

. p75NTR silencing inhibits proliferation, migration, and extracellular matrix deposition of hypertrophic scar fibroblasts by activating autophagy through inhibiting the PI3K/Akt/mTOR pathway. Can J Physiol Pharmacol. 2021;99:349-359.

46.

Wang

Kennedy

Wong

, et al. Aging inverts the effects of p75NTR-modulated mTOR manipulation on hippocampal neuron synaptic plasticity in male mice. Faseb J. 2023;37:e23067.

47.

Lupinacci

Perri

Toteda

, et al. Rapamycin promotes autophagy cell death of Kaposi’s sarcoma cells through P75NTR activation. Exp Dermatol. 2022;31:143-153.

48.

Hodges

Lugo

. Therapeutic role of targeting mTOR signaling and neuroinflammation in epilepsy. Epilepsy Res. 2020;161:106282.

49.

Samanta

. DEPDC5-related epilepsy: a comprehensive review. Epilepsy Behav. 2022;130:108678.

50.

Troca-Marín

Alves-Sampaio

Montesinos

. An increase in basal BDNF provokes hyperactivation of the Akt-mammalian target of rapamycin pathway and deregulation of local dendritic translation in a mouse model of Down’s syndrome. J Neurosci. 2011;31:9445-9455.

51.

Grande

Manassero

Vercelli

. Neuroprotective and anti-inflammatory roles of the phosphatase and tensin homolog deleted on chromosome ten (PTEN) inhibition in a mouse model of temporal lobe epilepsy. PLoS One. 2014;9:e114554.

52.

Ronzano

Scala

Abiusi

, et al. Phosphatase and tensin homolog (PTEN) variants and epilepsy: a multicenter case series. Seizure. 2022;100:82-86.

53.

Hartmann

Hunot

Michel

, et al. Caspase-3: a vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson’s disease. Proc Natl Acad Sci USA. 2000;97:2875-2880.

54.

Bradshaw

Nguyen

Wallace

, et al. Monitoring signaling by the p75NTR receptor utilizing a caspase-3 activation assay amenable to small-molecule screening. Assay Drug Dev Technol. 2012;10:353-364.

55.

Song

Volosin

Cragnolini

, et al. ProNGF induces PTEN via p75NTR to suppress Trk-mediated survival signaling in brain neurons. J Neurosci. 2010;30:15608-15615.

56.

Schindler

Pearson

Bonner

, et al. Caspase-3 cleavage and nuclear localization of caspase-activated DNase in human temporal lobe epilepsy. J Cereb Blood Flow Metab. 2006;26:583-589.

57.

Henshall

Clark

Adelson

, et al. Alterations in bcl-2 and caspase gene family protein expression in human temporal lobe epilepsy. Neurology. 2000;55:250-257.

58.

Henshall

Simon

. Epilepsy and apoptosis pathways. J Cereb Blood Flow Metab. 2005;25:1557-1572.

59.

Liou

Clark

Henshall

, et al. To die or not to die for neurons in ischemia, traumatic brain injury and epilepsy: a review on the stress-activated signaling pathways and apoptotic pathways. Prog Neurobiol. 2003;69:103-142.

60.

Narkilahti

Nissinen

Pitkänen

. Administration of caspase 3 inhibitor during and after status epilepticus in rat: effect on neuronal damage and epileptogenesis. Neuropharmacology. 2003;44:1068-1088.

61.

Muzyka

Men’shanov

Bannova

, et al. The interrelationship between BDNF and its precursor and the level of active caspase-3 in the brain regions of neonatal rats. Neurochemical Journal. 2012;6:260-264.

62.

Lin

Zhang

, et al. Targeting NF-κB pathway for the therapy of diseases: mechanism and clinical study. Signal Transduct Targeted Ther. 2020;5:209.

63.

Barnabei

Laplantine

Mbongo

, et al. NF-κB: at the borders of autoimmunity and inflammation. Front Immunol. 2021;12:716469.

64.

Zhang

, et al. NF-κB signaling in inflammation and cancer. MedComm. 2021;2:618-653.

65.

Bai

Yang

, et al. p75NTR activation of NF-κB is involved in PrP106-126-induced apoptosis in mouse neuroblastoma cells. Neurosci Res. 2008;62:9-14.

66.

Cai

Lin

. The function of NF-kappa B during epilepsy, a potential therapeutic target. Front Neurosci. 2022;16:851394.

67.

Lerner-Natoli

Montpied

Rousset

M-C

, et al. Sequential expression of surface antigens and transcription factor NFκB by hippocampal cells in excitotoxicity and experimental epilepsy. Epilepsy Res. 2000;41:141-154.

68.

Wang

Yan

Wang

, et al. Dynamic regulation effect of long non-coding RNA-UCA1 on NF-kB in hippocampus of epilepsy rats. Eur Rev Med Pharmacol Sci. 2017;21:3113-3119.

69.

Huang

X-y

Q-p

Shi

H-y

, et al. Everolimus inhibits PI3K/Akt/mTOR and NF-kB/IL-6 signaling and protects seizure-induced brain injury in rats. J Chem Neuroanat. 2021;114:101960.

70.

Yang

Wang

Nie

, et al. proBDNF expression induces apoptosis and inhibits synaptic regeneration by regulating the RhoA-JNK pathway in an in vitro post-stroke depression model. Transl Psychiatry. 2021;11:578.

71.

Schmidt

Blaabjerg

Freude

, et al. RhoA signaling in neurodegenerative diseases. Cells. 2022;11:1520.

72.

Lemkuil

Head

Pearn

, et al. Isoflurane neurotoxicity is mediated by p75NTR-RhoA activation and actin depolymerization. The Journal of the American Society of Anesthesiologists. 2011;114:49-57.

73.

Miguez

Garcia-Diaz

Brito

, et al. Fingolimod (FTY720) enhances hippocampal synaptic plasticity and memory in Huntington’s disease by preventing p75NTR up-regulation and astrocyte-mediated inflammation. Hum Mol Genet. 2015;24:4958-4970.

74.

Yamaguchi

Nakao

Arima

, et al. Rho-kinase/ROCK as a potential drug target for vitreoretinal diseases. Journal of ophthalmology. 2017;2017:8543592.

75.

Bai

Zhou

Ouyang

, et al. A de novo mutation in the MTUS1 gene decreases the risk of non-compaction of ventricular myocardium via the Rac1/Cdc42 pathway. Frontiers in Pediatrics. 2019;7:247.

76.

Hamano

Shirafuji

Yen

S-H

, et al. Rho-kinase ROCK inhibitors reduce oligomeric tau protein. Neurobiol Aging. 2020;89:41-54.

77.

Fujita

Yamashita

. Axon growth inhibition by RhoA/ROCK in the central nervous system. Front Neurosci. 2014;8:338.

78.

Dubreuil

Marklund

Deschamps

, et al. Activation of Rho after traumatic brain injury and seizure in rats. Exp Neurol. 2006;198:361-369.

79.

Xiang

Niu

Xie

, et al. Inhibition of RhoA/Rho kinase signaling pathway by fasudil protects against kainic acid-induced neurite injury. Brain and Behavior. 2021;11:e2266.

80.

Kourdougli

Varpula

Chazal

, et al. Detrimental effect of post Status Epilepticus treatment with ROCK inhibitor Y-27632 in a pilocarpine model of temporal lobe epilepsy. Front Cell Neurosci. 2015;9:413.

81.

Forgione

Fehlings

. Rho-ROCK inhibition in the treatment of spinal cord injury. World Neurosurg. 2014;82:e535-e539.

82.

Naska

Lin

Miller

, et al. p75NTR is an obligate signaling receptor required for cues that cause sympathetic neuron growth cone collapse. Mol Cell Neurosci. 2010;45:108-120.

83.

Zeng

J-J

Zhou

X-F

, et al. Roles of p75NTR in the pathogenesis of Alzheimer’s disease: a novel therapeutic target. Biochem Pharmacol. 2011;82:1500-1509.

The functional and molecular roles of p75 neurotrophin receptor (p75 NTR ) in epilepsy

Abstract

Plain Language Summary

Keywords

Introduction

Role of p75NTR in epilepsy

Mechanistic pathways of p75NTR in epilepsy

PI3K/Aκt

Caspase 3 and p75NTR

NF-κB and p75NTR

Ras homology family member A/Rho/ROCK and p75NTR

Conclusions

Footnotes

Author contributions

Declaration of conflicting interests

Funding

ORCID iD

Data availability statement

References

Role of p75^NTR in epilepsy

Mechanistic pathways of p75^NTR in epilepsy

Caspase 3 and p75^NTR

NF-κB and p75^NTR

Ras homology family member A/Rho/ROCK and p75^NTR