Evidence map›Paper›PMID 29520378›Full record

ArticleJACC. Basic to translational science2017

Cardiosphere-Derived Cells Demonstrate Metabolic Flexibility That Is Influenced by Adhesion Status.

Junaid Afzal, Angel Chan, Mehmet Fatih Karakas, Kirubel Woldemichael, Styliani Vakrou, Yufan Guan, Jeffrey Rathmell, Richard Wahl, Martin Pomper, D Brian Foster and 4 more

Open access · goldAbstract read
In one paragraph

Article in JACC. Basic to translational science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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.

Junaid AfzalDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Angel ChanDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Mehmet Fatih KarakasDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Kirubel WoldemichaelDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Styliani VakrouDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Yufan GuanDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Jeffrey RathmellDepartment of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee.
Richard WahlDepartment of Radiology, Washington University School of Medicine, St. Louis, Missouri.
Martin PomperDepartment of Radiology, Johns Hopkins School of Medicine, Baltimore, Maryland.
D Brian FosterDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Miguel A AonDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Benjamin TsuiDepartment of Radiology, Johns Hopkins School of Medicine, Baltimore, Maryland.
Brian O'RourkeDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
M Roselle AbrahamDepartment of Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland.
Johns Hopkins University · USJohns Hopkins Medicine · USNational Institute on Aging · USVanderbilt University Medical Center · USWashington University in St. Louis · US

Funding

Institute for Clinical and Translational Research (UL1)UL1RR025005 · NCRR · JOHNS HOPKINS UNIVERSITY · PI FORD, DANIEL ERNEST · 2007 to 2011
$75.8M
PATHOPHYSIOLOGY OF MYOCARDIAL DISEASEST32HL007227 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI Chulan Kwon, WENDY S POST · 1985 to 2026
$21.2M
Imaging of the Myocardial Microenvironment to Facilitate Stem Cell EngraftmentR01HL092985 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI ABRAHAM, MARIA ROSELLE, WAHL, RICHARD LEO · 2010 to 2014
$2.3M
NCRR NIH HHS UL1 RR025005NHLBI NIH HHS R01 HL092985NHLBI NIH HHS T32 HL007227
6 · The paper itself

Abstract

Adult stem cells demonstrate metabolic flexibility that is regulated by cell adhesion status. The authors demonstrate that adherent cells primarily utilize glycolysis, whereas suspended cells rely on oxidative phosphorylation for their ATP needs. Akt phosphorylation transduces adhesion-mediated regulation of energy metabolism, by regulating translocation of glucose transporters (GLUT1) to the cell membrane and thus, cellular glucose uptake and glycolysis. Cell dissociation, a pre-requisite for cell transplantation, leads to energetic stress, which is mediated by Akt dephosphorylation, downregulation of glucose uptake, and glycolysis. They designed hydrogels that promote rapid cell adhesion of encapsulated cells, Akt phosphorylation, restore glycolysis, and cellular ATP levels.

Indexed as

cardiosphere-derived cells (CDCs)glycolysismetabolismoxidative phosphorylation (OxPhos)sodium-iodide symporter (NIS)SPECT imaging

Identifiers

PMID29520378
PMCPMC5839118
OpenAlexW2766836549

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.