Evidence map›Paper›PMID 9105039›Full record

ArticleThe Journal of cell biology1997

Lysosomes behave as Ca2+-regulated exocytic vesicles in fibroblasts and epithelial cells.

A Rodríguez, P Webster, J Ortego, N W Andrews

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 229 papers.

0numbers the graph read from it
0cells of the map it votes in
229citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

229 citing papers in PubMed, 530 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Autophagy-lysosomal pathway in neurodegeneration.Molecular neurodegeneration advances · 2026
    Review
  8. Review
  9. Review
  10. Molecular biology of the cell · 2025
    Article
  11. Article
  12. Canonical and noncanonical autophagy: involvement in Parkinson's disease.Frontiers in cell and developmental biology · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

169 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

4 authors at 1 institution in 1 country.

A RodríguezDepartment of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06520, USA.
P Webster
J Ortego
N W Andrews
Yale University · US

Funding

Lyosome Mediated Cell Invasion by Trypanosoma CruziR37AI034867 · NIAID · YALE UNIVERSITY · PI ANDREWS, NORMA WINDSOR · 2003 to 2012
$4.5M
LYSOSOME-MEDIATED CELL INVASION BY TRYPANOSOMA CRUZIR01AI034867 · NIAID · YALE UNIVERSITY · PI ANDREWS, NORMA WINDSOR · 1994 to 2003
$880k
NIAID NIH HHS R01 AI034867NIAID NIH HHS R01 AI34867NIAID NIH HHS R37 AI034867
6 · The paper itself

Abstract

Lysosomes are considered to be a terminal degradative compartment of the endocytic pathway, into which transport is mostly unidirectional. However, specialized secretory vesicles regulated by Ca2+, such as neutrophil azurophil granules, mast cell-specific granules, and cytotoxic lymphocyte lytic granules, share characteristics with lysosomes that may reflect a common biogenesis. In addition, the involvement of Ca2+ transients in the invasion mechanism of the parasite Trypanosoma cruzi, which occurs by fusion of lysosomes with the plasma membrane, suggested that lysosome exocytosis might be a generalized process present in most cell types. Here we demonstrate that elevation in the intracellular free Ca2+ concentration of normal rat kidney (NRK) fibroblasts induces fusion of lysosomes with the plasma membrane. This was verified by measuring the release of the lysosomal enzyme beta-hexosaminidase, the appearance on the plasma membrane of the lysosomal glycoprotein lgp120, the release of fluid-phase tracers previously loaded into lysosomes, and the release of the lysosomally processed form of cathepsin D. Exposure to the Ca2+ ionophore ionomycin or addition of Ca2+-containing buffers to streptolysin O-permeabilized cells induced exocytosis of approximately 10% of the total lysosomes of NRK cells. The process was also detected in other cell types such as epithelial cells and myoblasts. Lysosomal exocytosis was found to require micromolar levels of Ca2+ and to be temperature and ATP dependent, similar to Ca2+-regulated secretory mechanisms in specialized cells. These findings highlight a novel role for lysosomes in cellular membrane traffic and suggest that fusion of lysosomes with the plasma membrane may be an ubiquitous form of Ca2+-regulated exocytosis.

Indexed as

Adenosine TriphosphateAnimalsAntigens, CDCalciumCathepsin DCell MembraneCell Membrane PermeabilityCells, CulturedDose-Response Relationship, DrugEndosomesEpithelial CellsEpitheliumExocytosisFibroblastsFluorescein-5-isothiocyanateFluorescent DyesAdenosine TriphosphateAntigens, CDCalciumCathepsin DFluorescein-5-isothiocyanateFluorescent DyesIonomycinIonophoresLysosomal-Associated Membrane Protein 1Lysosomal Membrane ProteinsMembrane GlycoproteinsReceptors, Transferrin

Identifiers

PMID9105039
PMCPMC2139854
OpenAlexW2102696072

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.