Evidence map›Paper›PMID 25882843›Full record

ArticleThe Journal of biological chemistry2015

Functional Effect of Pim1 Depends upon Intracellular Localization in Human Cardiac Progenitor Cells.

Kaitlen Samse, Jacqueline Emathinger, Nirmala Hariharan, Pearl Quijada, Kelli Ilves, Mirko Völkers, Lucia Ormachea, Andrea De La Torre, Amabel M Orogo, Roberto Alvarez and 7 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
2.9field-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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 31 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Expression of PIM1/ASK1 Molecular Pathway Related Genes in Ischemic Cardiomyopathy.Cardiovascular & hematological disorders drug targets · 2025
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Human CardioChimeras: Creation of a Novel "Next-Generation" Cardiac Cell.Journal of the American Heart Association · 2020
    Article
  10. Review
  11. Article
  12. Review
  13. Review
  14. Empowering human cardiac progenitor cells by P2YThe Journal of physiology · 2017
    Article
  15. Article
  16. Decline in cellular function of aged mouse c-kitThe Journal of physiology · 2017
    Article
  17. Article
  18. Pim1 Kinase Overexpression Enhances ckitJournal of the American College of Cardiology · 2016
    Article
  19. 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

17 authors at 3 institutions in 1 country.

Kaitlen SamseFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Jacqueline EmathingerFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Nirmala HariharanFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Pearl QuijadaFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Kelli IlvesFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Mirko VölkersFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Lucia OrmacheaFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Andrea De La TorreFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Amabel M Orogothe Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, California 92093, and.
Roberto AlvarezFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Shabana DinFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Sadia MohsinFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Megan MonsantoFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Kimberlee M FischerFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182.
Walter P Dembitskythe Sharp Memorial Hospital, San Diego, California 92123.
Åsa B Gustafssonthe Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California, San Diego, La Jolla, California 92093, and.
Mark A SussmanFrom the San Diego Heart Research Institute, San Diego State University, San Diego, California 92182, heartman4ever@icloud.com.
San Diego State University · USUniversity of Montana · USSharp Memorial Hospital · US

Funding

Surgery, Physiology and ImmunohistopathologyP01HL085577 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI GLEMBOTSKI, CHRIS · 2006 to 2017
$18.4M
GRADUATE TRAINING IN CELLULAR &MOLECULAR PHARMACOLOGYT32GM007752 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BROWN, JOAN HELLER, HANDEL, TRACY M · 1985 to 2023
$13.5M
Regulation of Signal Transduction to Treat Heart FailureR01HL067245 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2001 to 2021
$6.0M
Role of Bnip3 in Myocardial Ischemia/ReperfusionR01HL087023 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUSTAFSSON, ASA B. · 2007 to 2016
$3.8M
Stem Cell Signaling in the Pathologically Challenged MyocardiumR37HL091102 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2008 to 2017
$3.8M
Mcl-1 as an essential regulator of cardiac mitochondrial functionR01HL101217 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GUSTAFSSON, ASA B. · 2010 to 2013
$2.4M
Beta-adrenergic signaling: double edged sword of myocardial repairR01HL117163 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2013 to 2017
$1.9M
Antagonism of myocardial aging and senescence with Pim-1 kinaseR01HL105759 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2011 to 2015
$1.8M
Cardioprotection by optimizing mTOR activityR01HL113647 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2013 to 2016
$1.5M
Molecular Engineering of Damaged Myocardium To Enhance Regeneration And RepairR01HL113656 · NHLBI · SAN DIEGO STATE UNIVERSITY · PI SUSSMAN, MARK ALAN · 2012 to 2013
$667k
NHLBI NIH HHS P01HL085577NHLBI NIH HHS R01 HL067245NHLBI NIH HHS R01HL067245NHLBI NIH HHS R01HL087023NHLBI NIH HHS R01HL101217NHLBI NIH HHS R01 HL105759NHLBI NIH HHS R01HL105759NHLBI NIH HHS R01 HL113647NHLBI NIH HHS R01 HL113656NHLBI NIH HHS R01 HL117163NHLBI NIH HHS R01HL117163NHLBI NIH HHS R37 HL091102NHLBI NIH HHS R37HL091102NIGMS NIH HHS T32 GM007752
6 · The paper itself

Abstract

Human cardiac progenitor cells (hCPC) improve heart function after autologous transfer in heart failure patients. Regenerative potential of hCPCs is severely limited with age, requiring genetic modification to enhance therapeutic potential. A legacy of work from our laboratory with Pim1 kinase reveals effects on proliferation, survival, metabolism, and rejuvenation of hCPCs in vitro and in vivo. We demonstrate that subcellular targeting of Pim1 bolsters the distinct cardioprotective effects of this kinase in hCPCs to increase proliferation and survival, and antagonize cellular senescence. Adult hCPCs isolated from patients undergoing left ventricular assist device implantation were engineered to overexpress Pim1 throughout the cell (PimWT) or targeted to either mitochondrial (Mito-Pim1) or nuclear (Nuc-Pim1) compartments. Nuc-Pim1 enhances stem cell youthfulness associated with decreased senescence-associated β-galactosidase activity, preserved telomere length, reduced expression of p16 and p53, and up-regulation of nucleostemin relative to PimWT hCPCs. Alternately, Mito-Pim1 enhances survival by increasing expression of Bcl-2 and Bcl-XL and decreasing cell death after H2O2 treatment, thereby preserving mitochondrial integrity superior to PimWT. Mito-Pim1 increases the proliferation rate by up-regulation of cell cycle modulators Cyclin D, CDK4, and phospho-Rb. Optimal stem cell traits such as proliferation, survival, and increased youthful properties of aged hCPCs are enhanced after targeted Pim1 localization to mitochondrial or nuclear compartments. Targeted Pim1 overexpression in hCPCs allows for selection of the desired phenotypic properties to overcome patient variability and improve specific stem cell characteristics.

Indexed as

Gene Expression RegulationApoptosisbeta-GalactosidaseCell CycleCell NucleusCell ProliferationCell SurvivalCellular SenescenceGreen Fluorescent ProteinsHeartHeart FailureHeart VentriclesHumansLentivirusMitochondriaMyocardiumbeta-GalactosidaseGreen Fluorescent ProteinsPIM1 protein, humanProto-Oncogene Proteins c-pim-1agingapoptosisheart failurehuman cardiac progenitor cellPim1proliferationsenescence

Identifiers

PMID25882843
PMCPMC4447967
OpenAlexW1989420473

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.