Evidence map›Paper›PMID 20884174›Full record

ArticleJournal of autoimmunity2010

Successful modulation of type 2 diabetes in db/db mice with intra-bone marrow--bone marrow transplantation plus concurrent thymic transplantation.

Ming Li, Nader G Abraham, Luca Vanella, Yuming Zhang, Muneo Inaba, Naoki Hosaka, Sho-Ichi Hoshino, Ming Shi, Yoko Miyamoto Ambrosini, M Eric Gershwin and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of autoimmunity, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Stem Cell Replacement Improves Expression of SMP30 in db/db Mice.International journal of molecular sciences · 2015
    Article
  10. Article
  11. Stem cell transplantation improves aging-related diseases.Frontiers in cell and developmental biology · 2014
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Stem cell transplantation increases antioxidant effects in diabetic mice.International journal of biological sciences · 2012
    Article
  19. Review
  20. Article
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 3 institutions in 2 countries.

Ming LiDepartment of Stem Cell Disorders, Kansai Medical University, Moriguchi City, Osaka 570-8506, Japan.
Nader G Abraham
Luca Vanella
Yuming Zhang
Muneo Inaba
Naoki Hosaka
Sho-Ichi Hoshino
Ming Shi
Yoko Miyamoto Ambrosini
M Eric Gershwin
Susumu Ikehara
Kansai Medical University · JPUniversity of California, Davis · USUniversity of Toledo · US

Funding

Vasoregulatory Function of CYP2E1-Derived EicosanoidsP01HL034300 · NHLBI · NEW YORK MEDICAL COLLEGE · PI JIANG, HOULI · 1985 to 2015
$33.4M
Oxidative Stress and Vascular HO in DiabetesR01DK068134 · NIDDK · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI ABRAHAM, NADER G. · 2006 to 2010
$1.7M
NHLBI NIH HHS HL34300NHLBI NIH HHS HL55601NHLBI NIH HHS P01 HL034300NIDDK NIH HHS DK068134NIDDK NIH HHS R01 DK068134
6 · The paper itself

Abstract

There is increasing evidence that both autoimmune and autoinflammatory mechanisms are involved in the development of not only type 1 diabetes mellitus (T1 DM), but also type 2 diabetes mellitus (T2 DM). Our laboratory has focused on this concept, and in earlier efforts replaced the bone marrow cells (BMCs) of leptin receptor-deficient (db/db) mice, an animal model of T2DM, with those of normal C57BL/6 (B6) mice by IBM-BMT. However, the outcome was poor due to incomplete recovery of T cell function. Therefore, we hypothesized that intra-bone marrow-bone marrow transplantation plus thymus transplantation (IBM-BMT + TT) could be used to treat T2 DM by normalizing the T cell imbalance. Hence we addressed this issue by using such dual transplantation and demonstrate herein that seven weeks later, recipient db/db mice manifested improved body weight, reduced levels of blood glucose, and a reduction of plasma IL-6 and IL-1β. More importantly, this treatment regimen showed normal CD4/CD8 ratios, and increased plasma adiponectin levels, insulin sensitivity, and the number of insulin-producing cells. Furthermore, the expression of pancreatic pAKT, pLKB1, pAMPK and HO-1 was increased in the mice treated with IBM-BMT + TT. Our data show that IBM-BMT + TT treatment normalizes T cell subsets, cytokine imbalance and insulin sensitivity in the db/db mouse, suggesting that IBM-BMT + TT is a viable therapeutic option in the treatment of T2 DM.

Indexed as

ImmunotherapyAdiponectinAnimalsBlood GlucoseBone Marrow TransplantationDiabetes Mellitus, Type 2Disease Models, AnimalGene Expression RegulationHumansInsulin-Secreting CellsInterleukin-1betaInterleukin-6MiceMice, Inbred C57BLMice, Mutant StrainsReceptors, LeptinAdiponectinAdipoq protein, mouseBlood GlucoseInterleukin-1betaInterleukin-6Receptors, Leptin

Identifiers

PMID20884174
PMCPMC5553687
OpenAlexW2039469443

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.