Evidence map›Paper›PMID 32109377›Full record

ArticleCell stem cell2020

Restraining Lysosomal Activity Preserves Hematopoietic Stem Cell Quiescence and Potency.

Raymond Liang, Tasleem Arif, Svetlana Kalmykova, Artem Kasianov, Miao Lin, Vijay Menon, Jiajing Qiu, Jeffrey M Bernitz, Kateri Moore, Fangming Lin and 5 more

Abstract read
In one paragraph

Article in Cell stem cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 163 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

163 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Niches in cancer: from primary tumors to metastatic disease.Journal of hematology & oncology · 2026
    Review
  3. Article
  4. Article
  5. Loss of TCA cycle turning promotes stem cell function.bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Hematopoietic Stem Cell Metabolism during Stress and Aging.Advances in geriatric medicine and research · 2026
    Article
  8. Review
  9. Unveiling Lactylation: A Novel Frontier in Cancer Stemness and Therapy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Stem cell functionbioRxiv : the preprint server for biology · 2026
    Article
  18. Review
  19. Article
  20. Article

103 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Raymond LiangDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029; Developmental and Stem Cell Biology Multidisciplinary Training Area, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Tasleem ArifDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Svetlana KalmykovaCenter for Data-Intensive Biomedicine and Biotechnology, Skoltech Russian Federation, Skolkovo Institute of Science and Technology, Moscow 143026, Russia.
Artem KasianovCenter for Data-Intensive Biomedicine and Biotechnology, Skoltech Russian Federation, Skolkovo Institute of Science and Technology, Moscow 143026, Russia; The Institute for Information Transmission Problems RAS, Moscow 127051, Russia.
Miao LinDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Vijay MenonDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Jiajing QiuDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Jeffrey M BernitzDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Kateri MooreDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029.
Fangming LinDepartment of Pediatrics, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.
Deanna L BensonDepartment of Neuroscience and Microscopy CoRE, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Nikolaos TzavarasDepartment of Neuroscience and Microscopy CoRE, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Milind MahajanGenetics and Genomics Science, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Dmitri PapatsenkoCenter for Data-Intensive Biomedicine and Biotechnology, Skoltech Russian Federation, Skolkovo Institute of Science and Technology, Moscow 143026, Russia.
Saghi GhaffariDepartment of Cell, Developmental & Regenerative Biology, Icahn School of Medicine at Mount Sinai, New York, NY 10029; Developmental and Stem Cell Biology Multidisciplinary Training Area, Icahn School of Medicine at Mount Sinai, New York, NY 10029; Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA; Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA. Electronic address: saghi.ghaffari@mssm.edu.

Funding

(PQ5) Mitochondria in Leukemic Stem Cell Disease ProgressionR01CA205975 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GHAFFARI, SAGHI · 2016 to 2025
$3.9M
Mitochondria in the Regulation of Terminal ErythropoiesisR01HL136255 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI SAGHI GHAFFARI · 2017 to 2026
$3.8M
Interdisciplinary Training in Systems and Developmental Biology and Birth DefectsT32HD075735 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI JABS, ETHYLIN WANG · 2013 to 2022
$1.8M
NCI NIH HHS R01 CA205975NHLBI NIH HHS R01 HL136255NICHD NIH HHS T32 HD075735
6 · The paper itself

Abstract

Quiescence is a fundamental property that maintains hematopoietic stem cell (HSC) potency throughout life. Quiescent HSCs are thought to rely on glycolysis for their energy, but the overall metabolic properties of HSCs remain elusive. Using combined approaches, including single-cell RNA sequencing (RNA-seq), we show that mitochondrial membrane potential (MMP) distinguishes quiescent from cycling-primed HSCs. We found that primed, but not quiescent, HSCs relied readily on glycolysis. Notably, in vivo inhibition of glycolysis enhanced the competitive repopulation ability of primed HSCs. We further show that HSC quiescence is maintained by an abundance of large lysosomes. Repression of lysosomal activation in HSCs led to further enlargement of lysosomes while suppressing glucose uptake. This also induced increased lysosomal sequestration of mitochondria and enhanced the competitive repopulation ability of primed HSCs by over 90-fold in vivo. These findings show that restraining lysosomal activity preserves HSC quiescence and potency and may be therapeutically relevant.

Indexed as

Hematopoietic Stem CellsMitochondriaCell DivisionGlycolysisLysosomesdormancyfissionhematopoietic stem cellHSClabel retentionlysosomesmitochondriamitophagymTORquiescence

Identifiers

PMID32109377
PMCPMC8075247

What OpenQuestion holds

Textmetadata
LicenceTDM
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.