Evidence map›Paper›PMID 20937705›Full record

ArticleThe Journal of experimental medicine2010

The innate immune system in host mice targets cells with allogenic mitochondrial DNA.

Kaori Ishikawa, Noriko Toyama-Sorimachi, Kazuto Nakada, Mami Morimoto, Hirotake Imanishi, Mariko Yoshizaki, Shigemi Sasawatari, Mamoru Niikura, Keizo Takenaga, Hiromichi Yonekawa and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. Review
  3. Mitochondrial DNA lineages determine tumor progression through T cell reactive oxygen signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Cardiac Involvement in Mitochondrial Disorders.Current heart failure reports · 2023
    Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. mtDNA, Metastasis, and the Mitochondrial Unfolded Protein Response (UPRFrontiers in cell and developmental biology · 2017
    Review
  14. Article
  15. Review
  16. Review
  17. The mitochondria-targeted anti-oxidant MitoQ decreases ischemia-reperfusion injury in a murine syngeneic heart transplant model.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2015
    Article
  18. Article
  19. An exploratory analysis of mitochondrial haplotypes and allogeneic hematopoietic cell transplantation outcomes.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
    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

11 authors at 6 institutions in 1 country.

Kaori IshikawaGraduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba, Ibaraki 305-8572, Japan.
Noriko Toyama-Sorimachi
Kazuto Nakada
Mami Morimoto
Hirotake Imanishi
Mariko Yoshizaki
Shigemi Sasawatari
Mamoru Niikura
Keizo Takenaga
Hiromichi Yonekawa
Jun-Ichi Hayashi
National Center for Global Health and Medicine · JPUniversity of Tsukuba · JPJapan Society for the Promotion of Science · JPKyorin University · JPShimane University · JPTokyo Metropolitan Institute of Medical Science · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial DNA (mtDNA) has been proposed to be involved in respiratory function, and mtDNA mutations have been associated with aging, tumors, and various disorders, but the effects of mtDNA imported into transplants from different individuals or aged subjects have been unclear. We examined this issue by generating trans-mitochondrial tumor cells and embryonic stem cells that shared the syngenic C57BL/6 (B6) strain-derived nuclear DNA background but possessed mtDNA derived from allogenic mouse strains. We demonstrate that transplants with mtDNA from the NZB/B1NJ strain were rejected from the host B6 mice, not by the acquired immune system but by the innate immune system. This rejection was caused partly by NK cells and involved a MyD88-dependent pathway. These results introduce novel roles of mtDNA and innate immunity in tumor immunology and transplantation medicine.

Indexed as

Stem Cell TransplantationAgingAnimalsCarcinoma, Lewis LungCell Line, TumorDNA, MitochondrialEmbryonic Stem CellsGraft RejectionImmunity, InnateKiller Cells, NaturalMiceMice, Inbred NZBMutationMyeloid Differentiation Factor 88Neoplasm TransplantationTransplantation, HomologousDNA, MitochondrialMyd88 protein, mouseMyeloid Differentiation Factor 88

Identifiers

PMID20937705
PMCPMC2964578
OpenAlexW2099447598

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.