Evidence map›Paper›PMID 26582390›Full record

ArticleMolecular biology of the cell2016

mTOR controls lysosome tubulation and antigen presentation in macrophages and dendritic cells.

Amra Saric, Victoria E B Hipolito, Jason G Kay, Johnathan Canton, Costin N Antonescu, Roberto J Botelho

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

73 citing papers in PubMed, 137 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. mTOR Signaling in Macrophages: All Depends on the Context.International journal of molecular sciences · 2025
    Review
  8. Review
  9. Article
  10. Review
  11. Inhibition of mTOR differently modulates planar and subepithelial fibrogenesis in human conjunctival fibroblasts.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
    Article
  12. Article
  13. Virulence · 2024
    Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

13 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

6 authors at 3 institutions in 2 countries.

Amra SaricMolecular Science Program and Department of Chemistry and Biology, Ryerson University, Toronto, ON M5B 2K3, Canada.
Victoria E B HipolitoMolecular Science Program and Department of Chemistry and Biology, Ryerson University, Toronto, ON M5B 2K3, Canada.
Jason G KayDepartment of Oral Biology, University at Buffalo, Buffalo, NY 14214.
Johnathan CantonProgram in Cell Biology, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
Costin N AntonescuMolecular Science Program and Department of Chemistry and Biology, Ryerson University, Toronto, ON M5B 2K3, Canada.
Roberto J BotelhoMolecular Science Program and Department of Chemistry and Biology, Ryerson University, Toronto, ON M5B 2K3, Canada rbotelho@ryerson.ca.
Toronto Metropolitan University · CAHospital for Sick Children · CAUniversity at Buffalo, State University of New York · US

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Macrophages and dendritic cells exposed to lipopolysaccharide (LPS) convert their lysosomes from small, punctate organelles into a network of tubules. Tubular lysosomes have been implicated in phagosome maturation, retention of fluid phase, and antigen presentation. There is a growing appreciation that lysosomes act as sensors of stress and the metabolic state of the cell through the kinase mTOR. Here we show that LPS stimulates mTOR and that mTOR is required for LPS-induced lysosome tubulation and secretion of major histocompatibility complex II in macrophages and dendritic cells. Specifically, we show that the canonical phosphatidylinositol 3-kinase-Akt-mTOR signaling pathway regulates LPS-induced lysosome tubulation independently of IRAK1/4 and TBK. Of note, we find that LPS treatment augmented the levels of membrane-associated Arl8b, a lysosomal GTPase required for tubulation that promotes kinesin-dependent lysosome movement to the cell periphery, in an mTOR-dependent manner. This suggests that mTOR may interface with the Arl8b-kinesin machinery. To further support this notion, we show that mTOR antagonists can block outward movement of lysosomes in cells treated with acetate but have no effect in retrograde movement upon acetate removal. Overall our work provides tantalizing evidence that mTOR plays a role in controlling lysosome morphology and trafficking by modulating microtubule-based motor activity in leukocytes.

Indexed as

ADP-Ribosylation FactorsAnimalsAntigen PresentationDendritic CellsEndosomesFemaleLysosomesMacrophagesMiceMice, Inbred C57BLOncogene Protein v-aktPhosphatidylinositol 3-KinasesProtein TransportRAW 264.7 CellsSignal TransductionToll-Like Receptor 4ADP-Ribosylation FactorsmTOR protein, mouseOncogene Protein v-aktPhosphatidylinositol 3-KinasesToll-Like Receptor 4TOR Serine-Threonine Kinases

Identifiers

PMID26582390
PMCPMC4713134
OpenAlexW2192238419

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.