Evidence map›Paper›PMID 29891535›Full record

ArticleBlood2018

Aged murine hematopoietic stem cells drive aging-associated immune remodeling.

Hanna Leins, Medhanie Mulaw, Karina Eiwen, Vadim Sakk, Ying Liang, Michael Denkinger, Hartmut Geiger, Reinhold Schirmbeck

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
4.9field-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

64 citing papers in PubMed, 100 citations in OpenAlex.

  1. Article
  2. Hematopoietic Stem Cell Metabolism during Stress and Aging.Advances in geriatric medicine and research · 2026
    Article
  3. Article
  4. Article
  5. Research progress on blood therapy for anti-aging.Journal of advanced research · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Aging and immunity: the age-old tango.Genes & development · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Hanna LeinsDepartment of Internal Medicine I, University Hospital of Ulm, Ulm, Germany.
Medhanie MulawInstitute of Experimental Cancer Research, University Hospital of Ulm, Ulm, Germany.
Karina EiwenInstitute of Molecular Medicine, Stem Cell and Aging, Ulm University, Ulm, Germany.
Vadim SakkInstitute of Molecular Medicine, Stem Cell and Aging, Ulm University, Ulm, Germany.
Ying LiangDepartment of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY.
Michael DenkingerAGAPLESION Bethesda Hospital, Geriatric Research Unit and.
Hartmut GeigerInstitute of Molecular Medicine, Stem Cell and Aging, Ulm University, Ulm, Germany.
Reinhold SchirmbeckDepartment of Internal Medicine I, University Hospital of Ulm, Ulm, Germany.
Universität Ulm · DEUniversity Hospital Ulm · DECincinnati Children's Hospital Medical Center · USUniversity of Kentucky · US

Funding

Latexin function in the maintenance and regeneration of the hematopoietic systemR01HL124015 · NHLBI · UNIVERSITY OF KENTUCKY · PI LIANG, YING · 2016 to 2024
$3.6M
Cdc42, hematopoietic stem cell polarity, and cell fateR01DK104814 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI ZHENG, YI · 2016 to 2019
$2.0M
Lineage Determination and Tissue HomeOstasis in the aged Hematopoietic SystemR01AG040118 · NIA · CINCINNATI CHILDRENS HOSP MED CTR · PI GEIGER, HARTMUT, ZHENG, YI · 2011 to 2015
$1.7M
Genetic Reg. of Hematopoietic Stem Cell MobilizationR01HL076604 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI GEIGER, HARTMUT · 2004 to 2007
$1.2M
Young Stem Cell Potential in Aged MiceR21DK077762 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI GEIGER, HARTMUT · 2008 to 2009
$413k
Latexin in human hematopoietic stem cell expansionR21HL140213 · NHLBI · UNIVERSITY OF KENTUCKY · PI LIANG, YING · 2017 to 2018
$230k
NHLBI NIH HHS R01 HL076604NHLBI NIH HHS R01 HL124015NHLBI NIH HHS R21 HL140213NIA NIH HHS R01 AG040118NIDDK NIH HHS R01 DK104814NIDDK NIH HHS R21 DK077762
6 · The paper itself

Abstract

Aging-associated remodeling of the immune system impairs its functional integrity and contributes to increased morbidity and mortality in the elderly. Aging of hematopoietic stem cells (HSCs), from which all cells of the adaptive immune system ultimately originate, might play a crucial role in the remodeling of the aged immune system. We recently reported that aging of HSCs is, in part, driven by elevated activity of the small RhoGTPase Cdc42 and that aged HSCs can be rejuvenated in vitro by inhibition of the elevated Cdc42 activity in aged HSCs with the pharmacological compound CASIN. To study the quality of immune systems stemming selectively from young or aged HSCs, we established a HSC transplantation model in T- and B-cell-deficient young RAG1

Indexed as

AgingAnimalsCellular SenescenceCytoskeletal ProteinsFemaleGene Expression ProfilingGenes, RAG-1Graft SurvivalHematopoietic Stem CellsHematopoietic Stem Cell TransplantationLymphocyte SubsetsMiceMice, Inbred C57BLMice, Knockoutrho GTP-Binding ProteinsTissue DonorsCdc42ep1 protein, mouseCytoskeletal Proteinsrho GTP-Binding ProteinsVaccines, DNA

Identifiers

PMID29891535
PMCPMC6137572
OpenAlexW2808613102

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.