Bioactive sphingolipids: metabolism and function
Open accessAbstract
Sphingolipids (SLs) are essential constituents of eukaryotic cells. Besides playing structural roles in cellular membranes, some metabolites, including ceramide, sphingosine, and sphingosine-1-phosphate, have drawn attention as bioactive signaling molecules involved in the regulation of cell growth, differentiation, senescence, and apoptosis. Understanding the many cell regulatory functions of SL metabolites requires an advanced knowledge of how and where in the cell they are generated, converted, or degraded. This review will provide a short overview of the metabolism, localization, and compartmentalization of SLs. Also, a discussion on bioactive members of the SL family and inducers of SL enzymes that lead to ceramide generation will be presented.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Ceramides are bioactive sphingolipids involved in cell signaling, apoptosis, and membrane structure, and play a critical role in neurodegenerative diseases like Alzheimer's disease.
“Cers are bioactive sphingolipids involved in cell signaling, apoptosis, and membrane structure, playing a critical role in neurodegenerative diseases like AD. 22 , 23”
From Protective mechanisms against Alzheimer's disease in APOE3‐Christchurch homozygous astrocytes (2025) · cites this paper as [22]
The Abstract identifies ceramide as a bioactive sphingolipid and describes sphingolipids’ roles in membrane structure and signaling. “SLs as Bioactive Molecules” links ceramide signaling to apoptosis. But “Inducers of SL Enzymes” says ceramide has been linked to Alzheimer’s disease and neurodegeneration and may mediate an amyloid-β response; it does not establish the claimed critical role. (LLM, conf=0.88)
Experimental — accuracy not yet measured
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Functional rafts in cell membranes
Simons, K., & Ikonen, E. (1997) · Nature · doi:10.1038/42408 · Cited by 9,757 · cited 1× · see citing works
“namically cluster with sterols to form lipid microdomains or rafts, which function as hubs for effective signal transduction and protein sorting (1).”
Flagged first, then by citations
Cited by
Sorted by citations
Chipuk, J. E., McStay, G. P., Bharti, A., Kuwana, T., Clarke, C. J., Siskind, L. J., Obeid, L. M., & Green, D. R. (2012) · Cell · doi:10.1016/j.cell.2012.01.038 · Cited by 436 · see citing works
Lipid metabolism and storage in neuroglia: role in brain development and neurodegenerative diseases
Yang, D., Wang, X., Zhang, L., Fang, Y., Zheng, Q., Liu, X., Yu, W., Chen, S., Ying, J., & Hua, F. (2022) · Cell & Bioscience · doi:10.1186/s13578-022-00828-0 · Cited by 179 · see citing works
Bujak, R., Daghir-Wojtkowiak, E., Kaliszan, R., & Markuszewski, M. J. (2016) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2016.00035 · Cited by 81 · see citing works
Zabielski, P., Blachnio-Zabielska, A., Lanza, I. R., Gopala, S., Manjunatha, S., Jakaitis, D. R., Persson, X.-M., Gransee, J., Klaus, K. A., Schimke, J. M., et al. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00610.2012 · Cited by 30 · see citing works
Nutraceutical Properties of Chestnut Flours: Beneficial Effects on Skeletal Muscle Atrophy
Frati, A., Landi, D., Marinelli, C., Gianni, G., Fontana, L., Migliorini, M., Pierucci, F., Garcia-Gil, M., & Meacci, E. (2014) · Food Funct. · doi:10.1039/c4fo00353e · Cited by 23 · see citing works
Protective mechanisms against Alzheimer's disease in APOE3‐Christchurch homozygous astrocytes
Tian, X., Rivera, E. K., Hwang, I., Nikitina, A. A., Smith, J. A., Cho, Y. J., Sala‐Jarque, J., DuBose, A., Andriola, C., Gollan‐Myers, T., et al. (2025) · Alzheimer's & Dementia · doi:10.1002/alz.70589 · Cited by 7 · see citing works
- Authors
- Bartke, N., & Hannun, Y. A.
- Affiliations
- Medical University of South Carolina (US)
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 2009-04
- Volume
- 50
- Pages
- S91-S96
- ISSN
- 0022-2275 (ISSN-L)
- PMC
- PMC2674734
- OpenAlex
- W2096237954
- Cited by
- 683
- References
- 1
- Citations by year
- 2026: 20 · 2025: 32 · 2024: 27 · 2023: 32 · 2022: 44 · 2021: 55 · 2020: 47 · 2019: 52 · 2018: 46 · 2017: 30 · 2016: 31 · 2015: 47 · 2014: 30 · 2013: 39 · 2012: 46
- FWCI
- 2.75
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health (GM43825)
- National Cancer Institute (R01CA087584, CA87584)
- National Institute of General Medical Sciences (GM-43825)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sphingolipid Metabolism and Signaling
- Health Sciences › Medicine › Physiology › Lysosomal Storage Disorders Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- sphingolipids, ceramide, sphingosine, sphingosine-1-phosphate, sphingolipid metabolism, cell growth, cell differentiation, senescence, apoptosis, subcellular compartmentalization, enzyme inducers
- MeSH terms
- Animals, Biological Transport, Esterases, Humans, Phospholipases, Sphingolipids, Lipid Metabolism
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review