Evidence map›Paper›PMID 31924779›Full record

ArticleNature communications2020

Macropinocytosis drives T cell growth by sustaining the activation of mTORC1.

John C Charpentier, Di Chen, Philip E Lapinski, Jackson Turner, Irina Grigorova, Joel A Swanson, Philip D King

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.1field-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

45 citing papers in PubMed, 72 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Macropinosomes are a site of HIV-1 entry into primary CD4Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Cellular Regulation of Macropinocytosis.International journal of molecular sciences · 2024
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

7 authors at 1 institution in 1 country.

John C CharpentierDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.ORCID http://orcid.org/0000-0001-9488-8239
Di ChenDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.
Philip E LapinskiDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.
Jackson TurnerDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.
Irina GrigorovaDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.
Joel A SwansonDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA.ORCID http://orcid.org/0000-0003-0900-8212
Philip D KingDepartment of Microbiology and Immunology, University of Michigan Medical School, Ann Arbor, Michigan, 48109, USA. kingp@umich.edu.
University of Michigan · US

Funding

The Regulation of MacropinocytosisR35GM131720 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SWANSON, JOEL A · 2019 to 2023
$2.4M
The Regulation of MacropinocytosisR01GM110215 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SWANSON, JOEL A · 2014 to 2017
$1.3M
NIGMS NIH HHS R01 GM110215NIGMS NIH HHS R35 GM131720
6 · The paper itself

Abstract

Macropinocytosis is an evolutionarily-conserved, large-scale, fluid-phase form of endocytosis that has been ascribed different functions including antigen presentation in macrophages and dendritic cells, regulation of receptor density in neurons, and regulation of tumor growth under nutrient-limiting conditions. However, whether macropinocytosis regulates the expansion of non-transformed mammalian cells is unknown. Here we show that primary mouse and human T cells engage in macropinocytosis that increases in magnitude upon T cell activation to support T cell growth even under amino acid (AA) replete conditions. Mechanistically, macropinocytosis in T cells provides access of extracellular AA to an endolysosomal compartment to sustain activation of the mechanistic target of rapamycin complex 1 (mTORC1) that promotes T cell growth. Our results thus implicate a function of macropinocytosis in mammalian cell growth beyond Ras-transformed tumor cells via sustained mTORC1 activation.

Indexed as

Amino AcidsAnimalsCD4-Positive T-LymphocytesEndosomesGuanine Nucleotide Exchange FactorsHumansLysosomesMechanistic Target of Rapamycin Complex 1MiceMice, Inbred C57BLPinocytosisSignal TransductionT-LymphocytesAmino AcidsGuanine Nucleotide Exchange FactorsMechanistic Target of Rapamycin Complex 1Rasgrp1 protein, mouse

Identifiers

PMID31924779
PMCPMC6954116
OpenAlexW3000257769

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.