Evidence map›Paper›PMID 24796659›Full record

ArticleMolecular and cellular endocrinology2014

Distinct roles of HIF1A in endothelial adaptations to physiological and ambient oxygen.

Yi-Zhou Jiang, Yan Li, Kai Wang, Cai-Feng Dai, Shi-An Huang, Dong-Bao Chen, Jing Zheng

Open access · greenAbstract read
In one paragraph

Article in Molecular and cellular endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. [Hypoxia promotes differentiation of human induced pluripotent stem cells into embryoid bodiesNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2022
    Article
  5. Article
  6. Article
  7. LncRNA GAS5 activates the HIF1A/VEGF pathway by binding to TAF15 to promote wound healing in diabetic foot ulcers.Laboratory investigation; a journal of technical methods and pathology · 2021
    Article
  8. Review
  9. Article
  10. Epigenetics andFrontiers in genetics · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Preeclampsia does not alter vascular growth and expression of CD31 and vascular endothelial cadherin in human placentas.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2015
    Article
  18. 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

7 authors at 4 institutions in 2 countries.

Yi-Zhou JiangDepartment of Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715, United States.
Yan LiDepartment of Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715, United States.
Kai WangClinical and Translational Research Center, Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai 200040, PR China.
Cai-Feng DaiDepartment of Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715, United States.
Shi-An HuangDepartment of Cardiovascular Medicine, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong, PR China.
Dong-Bao ChenDepartment of Obstetrics and Gynecology, University of California, Irvine, CA 92697, United States; Department of Pathology, University of California, Irvine, CA 92697, United States.
Jing ZhengDepartment of Obstetrics and Gynecology, University of Wisconsin, Madison, WI 53715, United States; Department of Cardiovascular Medicine, Affiliated Hospital of Guangdong Medical College, Zhanjiang 524001, Guangdong, PR China. Electronic address: jzheng@wisc.edu.
University of Wisconsin–Madison · USGuangdong Medical College · CNShanghai First Maternity and Infant Hospital · CNUniversity of California, Irvine · US

Funding

Institutional Clinical and Translational Science AwardUL1TR000427 · NCATS · UNIVERSITY OF WISCONSIN-MADISON · PI DREZNER, MARC KENNETH · 2012 to 2016
$32.2M
Unified Cellular and Molecular CoreP01HD038843 · NICHD · UNIVERSITY OF WISCONSIN-MADISON · PI BIRD, IAN M. · 2001 to 2017
$14.4M
Actions of Estrogen on Uterine Artery EndotheliumR01HL070562 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, DONGBAO · 2001 to 2025
$6.3M
Caveolin-1, Caveolae and Placental AngiogenesisR01HL074947 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI CHEN, DONGBAO · 2004 to 2007
$1.3M
NCATS NIH HHS UL1 TR000427NCATS NIH HHS UL1TR000427NHLBI NIH HHS HL70562NHLBI NIH HHS R01 HL070562NHLBI NIH HHS R01 HL074947NHLBI NIH HHS R01 HL74947NICHD NIH HHS P01 HD038843NICHD NIH HHS P01 HD38843
6 · The paper itself

Abstract

Fetoplacental endothelial cells reside under physiological normoxic conditions (∼2-8% O2) in vivo. Under such conditions, cells are believed to sense O2 changes primarily via hypoxia inducible factor 1 α (HIF1A). However, little is known regarding the role of HIF1A in fetoplacental endothelial function under physiological normoxia. We recently reported that physiological chronic normoxia (PCN; 20-25 day, 3% O2) enhanced FGF2- and VEGFA-stimulated proliferation and migration of human umbilical vein endothelial cells (HUVECs) via the MEK/ERK1/2 and PI3K/AKT1 pathways compared to standard cell culture normoxia (SCN; ambient O2: ∼21% O2). Here, we investigated the action of HIF1A in regulating these cellular responses in HUVECs. HIF1A adenovirus infection in SCN-cells increased HIF1A protein expression, enhanced FGF2- and VEGFA-stimulated cell proliferation by 2.4 and 2.0-fold respectively, and promoted VEGFA-stimulated cell migration by 1.4-fold. HIF1A adenovirus infection in SCN-cells did not affect either basal or FGF2- and VEGFA-induced ERK1/2 activation, but it decreased basal AKT1 phosphorylation. Interestingly, HIF1A knockdown in PCN-cells via specific HIF1A siRNA transfection did not alter FGF2- and VEGFA-stimulated cell proliferation and migration, or ERK1/2 activation; however, it inhibited FGF2-induced AKT1 activation by ∼50%. These data indicate that HIF1A differentially regulates cell proliferation and migration, and ERK1/2 and AKT1 activation in PCN- and SCN-HUVECs. These data also suggest that HIF1A critically regulates cell proliferation and migration in SCN-, but not in PCN-HUVECs.

Indexed as

Adaptation, PhysiologicalAdenoviridaeCell HypoxiaCell MovementCell ProliferationFibroblast Growth Factor 2Gene Expression RegulationGenetic VectorsHumansHuman Umbilical Vein Endothelial CellsHypoxia-Inducible Factor 1, alpha SubunitMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3OxygenPhosphatidylinositol 3-KinasesAKT1 protein, humanFibroblast Growth Factor 2HIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMAPK1 protein, humanMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3OxygenPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktRNA, Small InterferingVascular Endothelial Growth Factor AVEGFA protein, humanEndothelial cellsGrowth factorsHIF1AHypoxiaProtein kinases

Identifiers

PMID24796659
PMCPMC4079002
OpenAlexW2119559705

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.