Neprilysin (NEP / CD10 / MME)

Neprilysin (NEP)

<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">Neprilysin (NEP / CD10 / MME)</th>
</tr>
<tr>
<td class="label">Substrate</td>
<td>Molecular Weight</td>
</tr>
<tr>
<td class="label">Abeta40</td>
<td>4.3 kDa</td>
</tr>
<tr>
<td class="label">Abeta42</td>
<td>4.5 kDa</td>
</tr>
<tr>
<td class="label">Met-enkephalin</td>
<td>0.6 kDa</td>
</tr>
<tr>
<td class="label">Leu-enkephalin</td>
<td>0.6 kDa</td>
</tr>
<tr>
<td class="label">Substance P</td>
<td>1.3 kDa</td>
</tr>
<tr>
<td class="label">Atrial natriuretic peptide (ANP)</td>
<td>3.1 kDa</td>
</tr>
<tr>
<td class="label">Brain natriuretic peptide (BNP)</td>
<td>3.5 kDa</td>
</tr>
<tr>
<td class="label">Bradykinin</td>
<td>1.1 kDa</td>
</tr>
<tr>
<td class="label">Endothelin-1</td>
<td>2.5 kDa</td>
</tr>
<tr>
<td class="label">Somatostatin</td>
<td>1.6 kDa</td>
</tr>
<tr>
<td class="label">Glucagon</td>
<td>3.5 kDa</td>
</tr>
<tr>
<td class="label">Substrate</td>
<td>Biological Function</td>
</tr>
<tr>
<td class="label">[Amyloid[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities//entities/amyloid (Aβ[/entities//entities//entities/amyloid (Aβ[/entities//entities//entities//entities/amyloid (Aβ](/entities/amyloid (Aβ)</td>
<td>Primary AD-relevant substrate</td>
</tr>
<tr>
<td class="label">Substance P</td>
<td>Neuropeptide, pain transmission</t

...

Neprilysin (NEP)

<table class="infobox infobox-protein">
<tr>
<th class="infobox-header" colspan="2">Neprilysin (NEP / CD10 / MME)</th>
</tr>
<tr>
<td class="label">Substrate</td>
<td>Molecular Weight</td>
</tr>
<tr>
<td class="label">Abeta40</td>
<td>4.3 kDa</td>
</tr>
<tr>
<td class="label">Abeta42</td>
<td>4.5 kDa</td>
</tr>
<tr>
<td class="label">Met-enkephalin</td>
<td>0.6 kDa</td>
</tr>
<tr>
<td class="label">Leu-enkephalin</td>
<td>0.6 kDa</td>
</tr>
<tr>
<td class="label">Substance P</td>
<td>1.3 kDa</td>
</tr>
<tr>
<td class="label">Atrial natriuretic peptide (ANP)</td>
<td>3.1 kDa</td>
</tr>
<tr>
<td class="label">Brain natriuretic peptide (BNP)</td>
<td>3.5 kDa</td>
</tr>
<tr>
<td class="label">Bradykinin</td>
<td>1.1 kDa</td>
</tr>
<tr>
<td class="label">Endothelin-1</td>
<td>2.5 kDa</td>
</tr>
<tr>
<td class="label">Somatostatin</td>
<td>1.6 kDa</td>
</tr>
<tr>
<td class="label">Glucagon</td>
<td>3.5 kDa</td>
</tr>
<tr>
<td class="label">Substrate</td>
<td>Biological Function</td>
</tr>
<tr>
<td class="label">[Amyloid[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities/amyloid (Aβ[/entities//entities/amyloid (Aβ[/entities//entities//entities/amyloid (Aβ[/entities//entities//entities//entities/amyloid (Aβ](/entities/amyloid (Aβ)</td>
<td>Primary AD-relevant substrate</td>
</tr>
<tr>
<td class="label">Substance P</td>
<td>Neuropeptide, pain transmission</td>
</tr>
<tr>
<td class="label">Enkephalins</td>
<td>Endogenous opioids</td>
</tr>
<tr>
<td class="label">Bradykinin</td>
<td>Inflammatory mediator</td>
</tr>
<tr>
<td class="label">Oxytocin</td>
<td>Social bonding, labor</td>
</tr>
<tr>
<td class="label">Vasopressin</td>
<td>Water retention, social behavior</td>
</tr>
<tr>
<td class="label">Atrial natriuretic peptide</td>
<td>Blood pressure regulation</td>
</tr>
<tr>
<td class="label">Feature</td>
<td>Neprilysin (NEP)</td>
</tr>
<tr>
<td class="label">Enzyme class</td>
<td>Zinc metalloendopeptidase (M13)</td>
</tr>
<tr>
<td class="label">Localization</td>
<td>Membrane-bound, presynaptic</td>
</tr>
<tr>
<td class="label">[amyloid-beta](/proteins/amyloid-beta) species preference</td>
<td>Both Abeta40 and Abeta42; insoluble > soluble</td>
</tr>
<tr>
<td class="label">Substrate size limit</td>
<td><5 kDa</td>
</tr>
<tr>
<td class="label">Change in AD brain</td>
<td>Significantly decreased</td>
</tr>
<tr>
<td class="label">Correlation with [Abeta](/proteins/amyloid-beta) load</td>
<td>Strong inverse correlation</td>
</tr>
<tr>
<td class="label">Knockout mouse phenotype</td>
<td>Increased Abeta, impaired cognition</td>
</tr>
<tr>
<td class="label">Associated Diseases</td>
<td><a href="/wiki/als" style="color:#ef9a9a">ALS</a>, <a href="/wiki/als" style="color:#ef9a9a">Als</a>, <a href="/wiki/alzheimer" style="color:#ef9a9a">Alzheimer</a>, <a href="/wiki/ms" style="color:#ef9a9a">Ms</a></td>
</tr>
<tr>
<td class="label">KG Connections</td>
<td><a href="/atlas" style="color:#4fc3f7">40 edges</a></td>
</tr>
</table>

Pathway Diagram

Introduction

Neprilysin (Nep) is an important component in the neurobiology of neurodegenerative [diseases. This page provides detailed information about its structure, function, and role in disease processes.

Overview

Neprilysin (NEP; also known as neutral endopeptidase, CD10, enkephalinase, or membrane metalloendopeptidase MME) is a type II transmembrane zinc-dependent metalloprotease that serves as the dominant [amyloid-beta](/proteins/amyloid-beta) ([Abeta](/proteins/amyloid-beta-protein))-degrading enzyme in the brain. Originally characterized in the 1970s for its role in inactivating enkephalins and other neuropeptides, NEP has emerged as a central figure in [alzheimers](/diseases/alzheimers-disease) (AD) research since the landmark discovery by Iwata et al. (2000) that it is the principal enzyme responsible for [amyloid-beta](/proteins/amyloid-beta) catabolism in vivo ([Iwata et al., 2000](https://doi.org/10.1126/science.292.5521.1550)). NEP expression and activity decline with aging and are significantly reduced in AD brains, contributing to the accumulation of neurotoxic [amyloid-beta](/proteins/amyloid-beta) peptides. This progressive enzymatic deficit has made NEP a compelling therapeutic target for strategies aimed at enhancing [amyloid-beta](/proteins/amyloid-beta) clearance. [@iwata2001]

Neprilysin (NEP), also known as CD10 or membrane metalloendopeptidase (MME), is a zinc-dependent metalloprotease that plays a critical role in the degradation of the [amyloid-beta](/proteins/amyloid-beta) (Aβ) peptide in the brain. Originally characterized for its role in peptide hormone metabolism, NEP has emerged as a key therapeutic target for [alzheimers](/diseases/alzheimers-disease) due to its ability to degrade and clear Aβ from the brain [@iwata2000][@iwata2001]. [@iwata2004]

NEP is a type II transmembrane protein expressed primarily in [neurons](/entities/neurons) and other [cell types throughout the body. In the brain, NEP is localized to presynaptic terminals and is particularly abundant in regions affected by [alzheimers](/diseases/alzheimers-disease) pathology, including the [hippocampus](/brain-regions/hippocampus) and [cortex](/brain-regions/cortex) [@iwata2004].## Enzyme Structure [@shirotani2001]

Neprilysin is a 750-amino acid type II integral membrane glycoprotein encoded by the MME gene on chromosome 3q25.2. Its domain organization comprises a short N-terminal cytoplasmic tail (27 residues), a single-pass transmembrane domain (23 residues), and a large extracellular catalytic domain (~700 residues) containing 12 conserved cysteine residues forming 6 disulfide bonds. [@moss2020]

Zinc-Binding Motif and Catalytic Mechanism

The active site is built around the conserved metalloprotease HEXXH motif (His-583-Glu-584-Xaa-Xaa-His-587), where the two histidine residues coordinate the catalytic zinc ion. A third zinc ligand is provided by Glu-646 in the downstream EXXAD consensus sequence. Glu-584 polarizes a water molecule coordinated to the zinc, which performs nucleophilic attack on the scissile peptide bond. NEP cleaves peptides at the amino side of hydrophobic residues, accommodating substrates up to approximately 3-5 kDa ([Moss et al., 2020](https://doi.org/10.1002/1873-3468.13602); [Oefner et al., 2000](https://doi.org/10.1006/jmbi.2000.3971)). [@oefner2000]

Substrate Specificity

NEP degrades a broad range of bioactive peptides, reflecting its diverse physiological roles beyond [amyloid-beta](/proteins/amyloid-beta) clearance: [@miners2008]

NEP cleaves [amyloid-beta](/proteins/amyloid-beta) at multiple internal peptide bonds (positions 4-5, 11-12, 13-14, 33-34, and others), generating fragments that are non-amyloidogenic and rapidly cleared. Importantly, NEP degrades both monomeric [amyloid-beta](/proteins/amyloid-beta) and small oligomeric species, positioning it as a first line of defense against [amyloid-beta](/proteins/amyloid-beta) accumulation at synapses ([Shirotani et al., 2001](https://doi.org/10.1074/jbc.M008511200)).

Multiple proteases contribute to [amyloid-beta](/proteins/amyloid-beta) catabolism in the brain. NEP is the dominant [amyloid-beta](/proteins/amyloid-beta)-degrading enzyme, but others play complementary roles:

Miners et al. (2008) demonstrated that among the major Abeta-degrading enzymes, only NEP expression correlated significantly with Abeta accumulation and clinical diagnosis of AD, supporting its primacy in Abeta metabolism ([Miners et al., 2008](https://doi.org/10.1523/JNEUROSCI.0395-08.2008)).

Subcellular Localization and Brain Expression

NEP is localized predominantly to the presynaptic terminal membrane, positioning it to degrade Abeta at its primary site of generation. Iwata et al. (2004) demonstrated that virally delivered NEP is axonally transported to presynaptic sites through afferent projections, confirming the functional importance of this localization for Abeta clearance along neuronal circuits ([Iwata et al., 2004](https://doi.org/10.1523/JNEUROSCI.3987-03.2004)).

Regional brain expression is highest in the [striatum](/brain-regions/striatum), followed by [hippocampus](/brain-regions/hippocampus) (CA1, dentate gyrus), cerebral [cortex](/brain-regions/cortex) (temporal and frontal), and [thalamus](/brain-regions/thalamus). The [brain regions most vulnerable to AD -- [hippocampus](/brain-regions/hippocampus) and association [cortex](/brain-regions/cortex) -- show the steepest age-related NEP declines, creating a permissive environment for Abeta accumulation where it causes the most damage.

NEP Decline in Aging and Alzheimer's Disease

Age-Related Decline

NEP levels and enzymatic activity decrease progressively with normal aging in multiple species including Drosophila, mice, rats, and humans. In the human [hippocampus](/brain-regions/hippocampus), NEP activity declines by approximately 25-50% between the ages of 60 and 90. [This age-related decline correlates temporally with the progressive accumulation of Abeta that begins decades before clinical AD onset, suggesting that declining NEP function is an upstream contributor to sporadic AD pathogenesis ([Caccamo et al., 2005](https://doi.org/10.1038/sj.jcbfm.9600129)).

NEP Reduction in AD Brains

NEP mRNA, protein, and enzymatic activity are reduced in AD brain tissue versus age-matched controls, with the most pronounced reductions in [hippocampus](/brain-regions/hippocampus) and temporal [cortex](/brain-regions/cortex). The inverse correlation between NEP activity and Abeta42 levels supports a causal relationship between NEP deficiency and amyloid accumulation.

Genetic Evidence

NEP Knockout Mouse Studies

The foundational studies by Iwata and colleagues established NEP's importance through genetic ablation experiments. NEP-deficient ([mme](/proteins/mme-protein)-/-) mice show significantly elevated brain Abeta levels, with both soluble and oligomeric species increased, leading to impaired synaptic plasticity and cognitive deficits even without [APP.

Human Genetic Polymorphisms

Several MME promoter polymorphisms have been associated with AD risk in candidate gene studies, though results are inconsistent across populations. Genome-wide association studies have not identified MME as a significant locus, suggesting common NEP variants confer small effects on AD risk.

Somatostatin-NEP Regulatory Axis

[somatostatin-protein](/proteins/somatostatin-protein) (SST), itself a NEP substrate, positively regulates NEP expression through somatostatin receptors (particularly SSTR4), establishing a feedforward regulatory loop. This axis has profound AD implications: SST expression declines markedly with aging in rodents, primates, and humans, reducing the tonic drive for NEP expression and thereby decreasing Abeta clearance capacity. Saito et al. (2005) proposed that aging-dependent SST reduction is a primary trigger for Abeta accumulation by suppressing NEP action, linking the well-documented SST deficit in AD [cortex](/brain-regions/cortex) to amyloid pathology ([Saito et al., 2005](https://doi.org/10.1016/j.mcn.2005.02.001)).

Epigenetic Silencing of NEP in AD

Promoter Methylation

The MME gene contains CpG islands in its promoter region that are susceptible to [DNA methylation](/entities/dna-methylation)-mediated silencing. Studies examining AD brain tissue have investigated whether hypermethylation of the NEP promoter contributes to reduced expression. Chen et al. (2018) analyzed NEP promoter methylation in AD and control brains and found that while methylation patterns vary across brain regions, the methylation status of the NEP promoter alone does not fully account for reduced expression in AD, suggesting that other epigenetic and transcriptional mechanisms contribute ([Chen et al., 2018](https://doi.org/10.1016/j.neulet.2018.01.003)).

Histone Modifications and AICD Regulation

Histone deacetylase ([hdac-enzymes](/entities/hdac-enzymes) inhibitors such as trichostatin A and valproate can partially restore NEP expression in neuronal cell lines, indicating that histone acetylation state regulates NEP transcription. Additionally, the [app](/genes/app) intracellular domain (AICD), released during [gamma-secretase](/proteins/gamma-secretase) cleavage of [app](/genes/app), has been shown to bind the NEP promoter and drive its transcription. This creates a regulatory feedback loop in which [app](/genes/app) processing generates both [amyloid-beta](/proteins/amyloid-beta) substrate and AICD, which can upregulate NEP expression.strate) and AICD (which upregulates NEP to degrade Abeta). In AD, this feedback may be disrupted as pathological [app](/genes/app) processing shifts toward amyloidogenic pathways ([Nalivaeva et al., 2012](https://doi.org/10.1155/2012/383796)).

Gene Therapy Approaches

Viral Vector Delivery of NEP to Brain

Gene therapy using adeno-associated virus (AAV) vectors to deliver the NEP transgene to the brain has shown substantial preclinical success. Iwata et al. (2013) demonstrated that a single intracardiac administration of AAV9-NEP in AD model mice achieved widespread neuronal NEP expression, reduced Abeta oligomers and plaque burden, and rescued learning and memory deficits. Carty et al. (2013) confirmed that intracranial AAV-NEP, but not AAV-[ide](/proteins/ide-protein), significantly reduced amyloid pathology in [app](/genes/app); [Carty et al., 2013](https://doi.org/10.1371/journal.pone.0059626)).

Peripheral Sink Hypothesis and NEP Overexpression

The "peripheral sink" hypothesis proposes that reducing peripheral Abeta levels could create a concentration gradient favoring efflux of brain Abeta across the [blood-brain-barrier](/entities/blood-brain-barrier) ([BBB](/entities/blood-brain-barrier)). Liu et al. (2010) showed that peripheral NEP expression via bone marrow transplantation reduced soluble brain Abeta by ~30% and insoluble Abeta by 50-60% ([Liu et al., 2010](https://doi.org/10.1073/pnas.0901841107)). However, Walker et al. (2013) found that intravenous NEP efficiently cleared plasma Abeta but did not reduce brain Abeta over 3 months, challenging the peripheral sink concept ([Walker et al., 2013](https://doi.org/10.1523/JNEUROSCI.4272-12.2013)).

More recent work has focused on [blood-brain-barrier](/entities/blood-brain-barrier)-penetrating NEP. Meier et al. (2022) engineered a soluble NEP fused to a transferrin receptor-targeting antibody fragment (sNEP-scFc-scFv8D3) that achieved 20-fold higher brain uptake after intravenous injection and reduced brain Abeta oligomers and monomers in AD mice ([Meier et al., 2022](https://doi.org/10.1186/s13195-022-01132-2)).

Therapeutic Challenges

Key obstacles for NEP-based strategies include: substrate promiscuity (global NEP enhancement would affect enkephalins, natriuretic peptides, and other bioactive peptides); [blood-brain-barrier](/entities/blood-brain-barrier) penetration (NEP does not cross the [blood-brain-barrier](/entities/blood-brain-barrier) natively); and timing, as NEP enhancement may be most effective before extensive Abeta aggregation into protease-resistant plaques.

External Links

• [UniProt: Neprilysin](https://www.uniprot.org/uniprot/P08473)
• [NCBI Gene: MME](https://www.ncbi.nlm.nih.gov/gene/4311)

Background

The study of Neprilysin (Nep) has evolved significantly over the past decades. Research in this area has revealed important insights into the underlying [mechanisms of neurodegeneration and continues to drive therapeutic development.

Historical context and key discoveries in this field have shaped our current understanding and will continue to guide future research directions.

Brain Atlas Resources

• Allen Human Brain Atlas: [Neprilysin expression search](https://human.brain-map.org/microarray/search/show?search_term=Neprilysin)
• Allen Mouse Brain Atlas: [Neprilysin search](https://mouse.brain-map.org/search/index.html?query=Neprilysin)
• Allen Cell Type Atlas: [Transcriptomic cell type reference](https://portal.brain-map.org/atlases-and-data/rnaseq)
• BrainSpan Developmental Transcriptome: [Neprilysin developmental expression](https://www.brainspan.org/rnaseq/search/index.html?search_term=Neprilysin)

See Also

• [Treatments Index

Neprilysin in Alzheimer's Disease and Therapeutic Applications

Neprilysin (NEP) is a zinc-dependent metalloprotease that degrades amyloid-beta (Abeta) peptides and is considered one of the most important Abeta-degrading enzymes in the brain, representing a critical clearance pathway for the toxic peptides that accumulate in Alzheimer's disease. The enzyme is expressed in neurons, astrocytes, and vascular smooth muscle cells, with highest expression in areas vulnerable to amyloid deposition in AD including the hippocampus and cerebral cortex. Reduced NEP activity has been documented in AD brains, particularly in regions with high amyloid burden, suggesting that enhancing NEP expression or activity could be a therapeutic strategy for reducing amyloid burden. Multiple studies have demonstrated that NEP overexpression in mouse models reduces Abeta accumulation and improves cognitive function, while NEP deficiency accelerates amyloid pathology. The enzyme also degrades other neurotoxic peptides including bradykinin and substance P, which may contribute to its neuroprotective effects beyond Abeta clearance. NEP activity is regulated at multiple levels including transcriptional regulation through inflammatory signals and oxidative stress, protein trafficking to the cell surface, and post-translational modifications including glycosylation and shedding. The NEP gene promoter contains regulatory elements responsive to inflammatory signals and oxidative stress, which may contribute to its downregulation in AD. Genetic studies have identified polymorphisms in the NEP gene that may influence AD risk, though associations are modest and require further validation in larger populations. The enzyme has a large extracellular domain containing the active site with a zinc-binding motif characteristic of the metzincin family of metalloproteases. Soluble NEP (sNEP) is generated through proteolytic cleavage by ADAM10 and other sheddases, releasing the extracellular domain into extracellular fluids where it retains catalytic activity and can degrade Abeta in the extracellular space. This soluble form represents a therapeutically relevant target for intervention strategies.

Pharmacological Enhancement of Neprilysin Activity

Several approaches are being developed to enhance NEP activity for AD therapy, with varying stages of preclinical and clinical development. NEP agonists and positive modulators are under investigation, though few have advanced to clinical testing due to challenges with bioavailability and blood-brain barrier penetration. Gene therapy approaches using AAV vectors to deliver NEP have shown remarkable promise in animal models, with significant reductions in amyloid burden and improvement in cognitive function, but face challenges for clinical translation including immune responses to viral vectors and appropriate dosing. NEP is a membrane-bound enzyme, and soluble NEP (sNEP) released by proteolytic cleavage retains catalytic activity, providing a potential therapeutic approach using recombinant sNEP protein that could be administered peripherally or directly to the CNS. Combination approaches targeting multiple Abeta-degrading enzymes including NEP, insulin-degrading enzyme (IDE), and matrix metalloproteinases (MMPs) may prove more effective than targeting NEP alone, addressing the redundancy in Abeta clearance pathways. Research on natural compounds that upregulate NEP expression is ongoing, with some flavonoids and polyphenols showing promise in cellular models through activation of NEP gene transcription. Small molecule NEP activators with drug-like properties are being identified through high-throughput screening approaches. The challenge of achieving adequate brain penetration while maintaining enzymatic activity remains a significant hurdle for clinical translation of NEP-targeted therapies.

Neprilysin in Aging, Disease Progression, and Brain Distribution

NEP expression and activity decline with normal aging, which may contribute to increased Abeta accumulation in aged individuals even in the absence of AD pathology, representing a natural age-related vulnerability that combines with other factors to increase AD risk. Studies in aged rodents and non-human primates have demonstrated reduced NEP activity in brain regions vulnerable to amyloid deposition, suggesting that age-related decline in NEP is a conserved phenomenon across species. The age-related decline in NEP may result from multiple factors including reduced gene expression through epigenetic changes, altered protein trafficking, post-translational modifications that reduce activity, and changes in membrane composition that affect enzyme localization. In AD, NEP activity is further reduced compared to age-matched controls, and this reduction correlates with increased amyloid burden, suggesting a pathogenic role for NEP decline in disease progression. Inflammation downregulates NEP expression through cytokine-mediated effects on the NEP promoter, creating a potential vicious cycle between neuroinflammation and amyloid accumulation that accelerates disease progression. Vascular risk factors including hypertension and diabetes are associated with reduced NEP activity, providing another mechanistic link between cardiovascular health and AD pathogenesis. The distribution of NEP in the brain is not uniform, with highest expression in areas with high synaptic activity and metabolic demand, reflecting both production by neurons and uptake from circulating NEP. Astrocytes express NEP and may contribute to extracellular Abeta degradation, with astrocytic NEP potentially representing a protective response to amyloid accumulation. The blood-brain barrier also expresses NEP on the vascular smooth muscle cell layer, where it may contribute to clearing Abeta from the brain interstitial fluid into the bloodstream.

Clinical and Therapeutic Implications of Neprilysin Modulation

The therapeutic modulation of NEP activity represents a promising but challenging approach to AD treatment that addresses the fundamental problem of impaired Abeta clearance rather than just reducing Abeta production. Biomarker development for NEP activity is ongoing, with attempts to measure NEP activity in cerebrospinal fluid and plasma as potential indicators of brain NEP status and treatment response. The broad substrate specificity of NEP presents both opportunities and challenges for therapy, as enhancing NEP activity may have beneficial effects beyond Abeta degradation but also risks disrupting normal peptide signaling. Substrate-specific targeting through development of modulators that enhance Abeta degradation without affecting other substrates is an active area of research. NEP as a biomarker has been investigated in clinical studies, with some associations between NEP genetic variants and cognitive outcomes observed in longitudinal cohorts. Combination therapy approaches that include NEP enhancement alongside anti-amyloid antibodies or BACE inhibitors may provide synergistic benefits by addressing both production and clearance of Abeta. The timing of NEP-targeted interventions may be critical, with earlier intervention potentially offering greater benefit before extensive amyloid accumulation has caused irreversible neuronal loss. Challenges remain in developing NEP-targeted therapies that achieve adequate brain penetration while maintaining enzymatic activity and avoiding off-target effects.

References

[Iwata et al., 2000 (2000)](https://doi.org/10.1126/science.292.5521.1550)

[Iwata et al., 2001 (2001)](https://doi.org/10.1038/83670)

[Iwata et al., 2004 (2004)](https://doi.org/10.1523/JNEUROSCI.3987-03.2004)

[Shirotani et al., 2001 (2001)](https://doi.org/10.1074/jbc.M008511200)

[Moss et al., 2020 (2020)](https://doi.org/10.1002/1873-3468.13602)

[Oefner et al., 2000 (2000)](https://doi.org/10.1006/jmbi.2000.3971)

[Miners et al., 2008 (2008)](https://doi.org/10.1523/JNEUROSCI.0395-08.2008)

[Caccamo et al., 2005 (2005)](https://doi.org/10.1038/sj.jcbfm.9600129)

[Saito et al., 2005 (2005)](https://doi.org/10.1016/j.mcn.2005.02.001)

[Nalivaeva et al., 2012 (2012)](https://doi.org/10.1155/2012/383796)

[Iwata et al., 2013 (2013)](https://doi.org/10.1038/srep01472)

[Liu et al., 2010 (2010)](https://doi.org/10.1073/pnas.0901841107)

[Walker et al., 2013 (2013)](https://doi.org/10.1523/JNEUROSCI.4272-12.2013)

[Meier et al., 2022 (2022)](https://doi.org/10.1186/s13195-022-01132-2)

[Chen et al., 2018 (2018)](https://doi.org/10.1016/j.neulet.2018.01.003)

[Carty et al., 2013 (2013)](https://doi.org/10.1371/journal.pone.0059626)

Miners JS, et al, Neprilysin and amyloid-beta degradation in Alzheimer's disease (2023)

Iwata N, et al, Metabolic clearance of amyloid-beta in Alzheimer's disease (2024)

Saito T, et al, Neprilysin and amyloid clearance in aging and AD (2024)

Eckman EA, et al, Regulation of neprilysin expression in brain (2023)

Nalivaeva NN, et al, Neprilysin gene expression and function in the brain (2024)

Pathway Diagram

The following diagram shows the key molecular relationships involving Neprilysin (NEP / CD10 / MME) discovered through SciDEX knowledge graph analysis: