Evidence map›Paper›PMID 30467385›Full record

ReviewNature reviews. Neuroscience2019

Necroptosis and RIPK1-mediated neuroinflammation in CNS diseases.

Junying Yuan, Palak Amin, Dimitry Ofengeim

Abstract readReview
In one paragraph

Review in Nature reviews. Neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 565 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
565citing papers in PubMed, 3 pooled it
23.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

565 citing papers in PubMed, 3 syntheses or guidelines pooled it, 934 citations in OpenAlex.

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  11. Mechanisms, regulation and clinical relevance of necroptosis.Nature reviews. Molecular cell biology · 2026
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505 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Junying YuanDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA. junying_yuan@hms.harvard.edu.
Palak AminDepartment of Cell Biology, Harvard Medical School, Boston, MA, USA.
Dimitry OfengeimNeuroscience Research, Sanofi, Framingham, MA, USA.
Harvard University · USSanofi (United States) · US

Funding

Single cell RNA-seq analyses of age-related changes in glial cells and in ADRF1AG055521 · NIA · HARVARD MEDICAL SCHOOL · PI YUAN, JUNYING · 2017 to 2017
$2.9M
Investigating the neuroinflammatory role of RIP1 kinaseR01AG047231 · NIA · HARVARD MEDICAL SCHOOL · PI YUAN, JUNYING · 2014 to 2018
$2.2M
Investigating the mechanism of TNFalpha mediated cell death in oligodendrocytesR01NS082257 · NINDS · HARVARD MEDICAL SCHOOL · PI YUAN, JUNYING · 2013 to 2017
$1.9M
Investigating the role and mechanism of RIPK1 in mediating cerebrovascular pathology of ADR21AG059073 · NIA · HARVARD MEDICAL SCHOOL · PI YUAN, JUNYING · 2018 to 2019
$466k
NIA NIH HHS R01 AG047231NIA NIH HHS R21 AG059073NIA NIH HHS RF1 AG055521NINDS NIH HHS R01 NS082257
6 · The paper itself

Abstract

Apoptosis is crucial for the normal development of the nervous system, whereas neurons in the adult CNS are relatively resistant to this form of cell death. However, under pathological conditions, upregulation of death receptor family ligands, such as tumour necrosis factor (TNF), can sensitize cells in the CNS to apoptosis and a form of regulated necrotic cell death known as necroptosis that is mediated by receptor-interacting protein kinase 1 (RIPK1), RIPK3 and mixed lineage kinase domain-like protein (MLKL). Necroptosis promotes further cell death and neuroinflammation in the pathogenesis of several neurodegenerative diseases, including multiple sclerosis, amyotrophic lateral sclerosis, Parkinson disease and Alzheimer disease. In this Review, we outline the evidence implicating necroptosis in these neurological diseases and suggest that targeting RIPK1 might help to inhibit multiple cell death pathways and ameliorate neuroinflammation.

Indexed as

AnimalsBrainHumansInflammationNecroptosisNeurodegenerative DiseasesNeuronsPhosphorylationReceptor-Interacting Protein Serine-Threonine KinasesReceptor-Interacting Protein Serine-Threonine KinasesRIPK1 protein, human

Identifiers

PMID30467385
PMCPMC6342007
OpenAlexW2901410206

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.