Evidence map›Paper›PMID 19948719›Full record

ArticleThe Journal of biological chemistry2010

Disruption of inducible 6-phosphofructo-2-kinase ameliorates diet-induced adiposity but exacerbates systemic insulin resistance and adipose tissue inflammatory response.

Yuqing Huo, Xin Guo, Honggui Li, Huan Wang, Weiyu Zhang, Ying Wang, Huaijun Zhou, Zhanguo Gao, Sucheta Telang, Jason Chesney and 4 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

52 citing papers in PubMed, 88 citations in OpenAlex.

  1. Trial
  2. Article
  3. F26BP enables control of glycolysis rate independent of energy state.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. PFKFB3 protein in adipose tissue contributes to whole body glucose homeostasis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  6. Obesity elicits a unique metabolomic signature in human airway smooth muscle cells.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. PFKFB3-dependent glucose metabolism regulates 3T3-L1 adipocyte development.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  14. Article
  15. Review
  16. Adoptive transfer ofLiver research (Beijing, China) · 2020
    Article
  17. Review
  18. Article
  19. Review
  20. PFKFB3 in Smooth Muscle Promotes Vascular Remodeling in Pulmonary Arterial Hypertension.American journal of respiratory and critical care medicine · 2019
    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

14 authors at 5 institutions in 1 country.

Yuqing HuoFrom the Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota 55455. Electronic address: yuqing@umn.edu.
Xin Guothe Intercollegiate Faculty of Nutrition, Department of Nutrition and Food Science, Texas A&M University, College Station, Texas 77843.
Honggui Lithe Intercollegiate Faculty of Nutrition, Department of Nutrition and Food Science, Texas A&M University, College Station, Texas 77843.
Huan WangFrom the Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota 55455.
Weiyu ZhangFrom the Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota 55455.
Ying Wangthe Intercollegiate Faculty of Genetics, Department of Poultry Science, Texas A&M University, College Station, Texas 77843.
Huaijun Zhouthe Intercollegiate Faculty of Genetics, Department of Poultry Science, Texas A&M University, College Station, Texas 77843.
Zhanguo Gaothe Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808.
Sucheta Telangthe J. G. Brown Cancer Center, University of Louisville, Louisville, Kentucky 40202, and.
Jason Chesneythe J. G. Brown Cancer Center, University of Louisville, Louisville, Kentucky 40202, and.
Y Eugene Chenthe Cardiovascular Center, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48105.
Jianping Yethe Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808.
Robert S Chapkinthe Intercollegiate Faculty of Nutrition, Department of Nutrition and Food Science, Texas A&M University, College Station, Texas 77843.
Chaodong Wuthe Intercollegiate Faculty of Nutrition, Department of Nutrition and Food Science, Texas A&M University, College Station, Texas 77843. Electronic address: cdwu@tamu.edu.
Texas A&M University · USUniversity of Minnesota Medical Center · USPennington Biomedical Research Center · USUniversity of Louisville · USUniversity of Michigan–Ann Arbor · US

Funding

Leukocyte C2GIcNAcT-I in atherosclerosisR01HL080569 · NHLBI · UNIVERSITY OF MINNESOTA · PI HUO, YUQING · 2006 to 2009
$1.4M
Inhibition of leukocyte C2GlcNAcT--l reduces thrombosisR01HL078679 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI HUO, YUQING · 2004 to 2007
$1.2M
NHLBI NIH HHS HL080569NHLBI NIH HHS HL78679NHLBI NIH HHS R01 HL078679NHLBI NIH HHS R01 HL080569
6 · The paper itself

Abstract

Adiposity is commonly associated with adipose tissue dysfunction and many overnutrition-related metabolic diseases including type 2 diabetes. Much attention has been paid to reducing adiposity as a way to improve adipose tissue function and systemic insulin sensitivity. PFKFB3/iPFK2 is a master regulator of adipocyte nutrient metabolism. Using PFKFB3(+/-) mice, the present study investigated the role of PFKFB3/iPFK2 in regulating diet-induced adiposity and systemic insulin resistance. On a high-fat diet (HFD), PFKFB3(+/-) mice gained much less body weight than did wild-type littermates. This was attributed to a smaller increase in adiposity in PFKFB3(+/-) mice than in wild-type controls. However, HFD-induced systemic insulin resistance was more severe in PFKFB3(+/-) mice than in wild-type littermates. Compared with wild-type littermates, PFKFB3(+/-) mice exhibited increased severity of HFD-induced adipose tissue dysfunction, as evidenced by increased adipose tissue lipolysis, inappropriate adipokine expression, and decreased insulin signaling, as well as increased levels of proinflammatory cytokines in both isolated adipose tissue macrophages and adipocytes. In an in vitro system, knockdown of PFKFB3/iPFK2 in 3T3-L1 adipocytes caused a decrease in the rate of glucose incorporation into lipid but an increase in the production of reactive oxygen species. Furthermore, knockdown of PFKFB3/iPFK2 in 3T3-L1 adipocytes inappropriately altered the expression of adipokines, decreased insulin signaling, increased the phosphorylation states of JNK and NFkappaB p65, and enhanced the production of proinflammatory cytokines. Together, these data suggest that PFKFB3/iPFK2, although contributing to adiposity, protects against diet-induced insulin resistance and adipose tissue inflammatory response.

Indexed as

Insulin Resistance3T3-L1 CellsAdipocytesAdipose TissueAdiposityAnimalsBlotting, WesternDietary FatsInflammation MediatorsInsulinInterleukin-6LeptinMiceMice, Inbred C57BLMice, KnockoutPhosphofructokinase-2Dietary FatsInflammation MediatorsInsulinInterleukin-6Leptinperoxisome-proliferator-activated receptor-gamma coactivator-1Phosphofructokinase-2PPAR alphaTranscription FactorsTumor Necrosis Factor-alpha

Identifiers

PMID19948719
PMCPMC2823512
OpenAlexW2164548123

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.