Evidence map›Paper›PMID 18326892›Full record

ReviewJournal of lipid research2008

Nuclear sphingolipids: metabolism and signaling.

Robert W Ledeen, Gusheng Wu

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of lipid research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

52 citing papers in PubMed, 106 citations in OpenAlex.

  1. Toward an NGF-based therapy for Rett syndrome.Frontiers in neuroscience · 2026
    Review
  2. Review
  3. Article
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  6. Article
  7. Article
  8. Review
  9. The expanding organelle lipidomes: current knowledge and challenges.Cellular and molecular life sciences : CMLS · 2023
    Review
  10. SMPDL3b modulates radiation-induced DNA damage response in renal podocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Review
  16. S1P/S1P Receptor Signaling in Neuromuscolar Disorders.International journal of molecular sciences · 2019
    Review
  17. Review
  18. Review
  19. Review
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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

2 authors at 2 institutions in 1 country.

Robert W LedeenDepartment of Neurology & Neurosciences, New Jersey Medical School, The University of Medicine and Dentistry of New Jersey, Newark, NJ 07103, USA. ledeenro@umdnj.edu
Gusheng Wu
Rutgers New Jersey Medical SchoolUniversity Hospital, Newark · US

Funding

Role of Nuclear Gangliosides in Neuronal FunctionR01NS033912 · NINDS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI LEDEEN, ROBERT W · 1996 to 2012
$3.8M
NINDS NIH HHS 2R01 NS033912NINDS NIH HHS R01 NS033912
6 · The paper itself

Abstract

Sphingolipids are most prominently expressed in the plasma membrane, but recent studies have pointed to important signaling and regulatory roles in the nucleus. The most abundant nuclear sphingolipid is sphingomyelin (SM), which occurs in the nuclear envelope (NE) as well as intranuclear sites. The major metabolic product of SM is ceramide, which is generated by nuclear sphingomyelinase and triggers apoptosis and other metabolic changes. Ceramide is further hydrolyzed to free fatty acid and sphingosine, the latter undergoing conversion to sphingosine phosphate by action of a specific nuclear kinase. Gangliosides are another type of sphingolipid found in the nucleus, members of the a-series of gangliotetraose gangliosides (GM1, GD1a) occurring in the NE and endonuclear compartments. GM1 in the inner membrane of the NE is tightly associated with a Na(+)/Ca(2+) exchanger whose activity it potentiates, thereby contributing to regulation of Ca(2+) homeostasis in the nucleus. This was shown to exert a cytoprotective role as absence or inactivation of this nuclear complex rendered cells vulnerable to apoptosis. This was demonstrated in the greatly enhanced kainite-induced seizure activity in knockout mice lacking gangliotetraose gangliosides. The pathology included apoptotic destruction of neurons in the CA3 region of the hippocampus. Ca(2+) homeostasis was restored in these animals with LIGA-20, a membrane-permeant derivative of GM1 that entered the NE and activated the nuclear Na(+)/Ca(2+) exchanger. Some evidence suggests the presence of uncharged glycosphingolipids in the nucleus.

Indexed as

Signal TransductionAnimalsCarbohydrate SequenceCell NucleusHumansMolecular Sequence DataSphingolipidsSphingolipids

Identifiers

PMID18326892
PMCPMC2386903
OpenAlexW2093186342

What OpenQuestion holds

Textmetadata
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.