Evidence map›Paper›PMID 29746165›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2018

A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest.

Maura Samarani, Nicoletta Loberto, Giulia Soldà, Letizia Straniero, Rosanna Asselta, Stefano Duga, Giulia Lunghi, Fabio A Zucca, Laura Mauri, Maria Grazia Ciampa and 7 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

23 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
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  4. Review
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  9. Article
  10. Article
  11. Review
  12. Article
  13. Glycosphingolipids.Advances in experimental medicine and biology · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Synthesis and Therapeutic Applications of Iminosugars in Cystic Fibrosis.International journal of molecular sciences · 2020
    Review
  19. Article
  20. Article
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

17 authors at 3 institutions in 1 country.

Maura SamaraniDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Nicoletta LobertoDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Giulia SoldàDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Letizia StranieroDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Rosanna AsseltaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Stefano DugaDepartment of Biomedical Sciences, Humanitas University, Pieve Emanuele, Milan, Italy.
Giulia LunghiDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Fabio A ZuccaInstitute of Biomedical Technologies, National Research Council of Italy, Segrate, Italy.
Laura MauriDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Maria Grazia CiampaDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Domitilla SchiumariniDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Rosaria BassiDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Paola GiussaniDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Elena ChiricozziDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Alessandro PrinettiDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Massimo AureliDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
Sandro SonninoDepartment of Medical Biotechnology and Translational Medicine, University of Milan, Milan, Italy.
University of Milan · ITHumanitas University · ITInstitute of Biomedical Technologies · IT

Funding

Translational Science Laboratory Shared ResourceP30CA138313 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND N. DUBOIS · 2009 to 2026
$42.7M
THE ROLE OF LACTOSYLCERAMIDE IN RENAL AGING AND DISEASEP20RR017677 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SISKIND, LEAH J · 2002 to 2011
$23.4M
EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR018823 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND, JOHN R · 2003 to 2003
$2.9M
NCI NIH HHS P30 CA138313NCRR NIH HHS C06 RR018823NCRR NIH HHS P20 RR017677
6 · The paper itself

Abstract

Lysosomal accumulation of undegraded materials is a common feature of lysosomal storage diseases, neurodegenerative disorders, and the aging process. To better understand the role of lysosomal storage in the onset of cell damage, we used human fibroblasts loaded with sucrose as a model of lysosomal accumulation. Sucrose-loaded fibroblasts displayed increased lysosomal biogenesis followed by arrested cell proliferation. Notably, we found that reduced lysosomal catabolism and autophagy impairment led to an increase in sphingolipids ( i.e., sphingomyelin, glucosylceramide, ceramide, and the gangliosides GM3 and GD3), at both intracellular and plasma membrane (PM) levels. In addition, we observed an increase in the lysosomal membrane protein Lamp-1 on the PM of sucrose-loaded fibroblasts and a greater release of the soluble lysosomal protein cathepsin D in their extracellular medium compared with controls. These results indicate increased fusion between lysosomes and the PM, as also suggested by the increased activity of lysosomal glycosphingolipid hydrolases on the PM of sucrose-loaded fibroblasts. The inhibition of β-glucocerebrosidase and nonlysosomal glucosylceramidase, both involved in ceramide production resulting from glycosphingolipid catabolism on the PM, partially restored cell proliferation. Our findings indicate the existence of a new molecular mechanism underlying cell damage triggered by lysosomal impairment.-Samarani, M., Loberto, N., Soldà, G., Straniero, L., Asselta, R., Duga, S., Lunghi, G., Zucca, F. A., Mauri, L., Ciampa, M. G., Schiumarini, D., Bassi, R., Giussani, P., Chiricozzi, E., Prinetti, A., Aureli, M., Sonnino, S. A lysosome-plasma membrane-sphingolipid axis linking lysosomal storage to cell growth arrest.

Indexed as

Cell Cycle CheckpointsCathepsin DCell LineCell MembraneFibroblastsHumansLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsLysosomesSphingolipidsCathepsin DCTSD protein, humanLAMP1 protein, humanLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsSphingolipidscatabolismcell proliferationcell surfaceglycohydrolasesglycosphingolipids

Identifiers

PMID29746165
PMCPMC6133699
OpenAlexW2801181686

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.