Evidence map›Paper›PMID 38537433›Full record

ArticleCell calcium2024

Utilization of the genetically encoded calcium indicator Salsa6F in cardiac applications.

Karla M Márquez-Nogueras, Elisa Bovo, Jacy E Neczypor, Quan Cao, Aleksey V Zima, Ivana Y Kuo

Abstract read
In one paragraph

Article in Cell calcium, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Karla M Márquez-NoguerasDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA.
Elisa BovoDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA.
Jacy E NeczyporDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA.
Quan CaoDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA.
Aleksey V ZimaDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA.
Ivana Y KuoDepartment of Cell and Molecular Physiology, and Cardiovascular Research Institute, Stritch School of Medicine, Loyola University Chicago, 2160 S. First Ave, Maywood, IL, USA. Electronic address: ikuo@luc.edu.

Funding

Activation of the Angiopoietin-Tie2/TEK Pathway to Treat Ocular Hypertension and GlaucomaR01EY025799 · NEI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JIN, JING, QUAGGIN, SUSAN E. · 2016 to 2024
$5.8M
Training Core for Chicago KUH FORWARDTL1DK132769 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Tamara Isakova · 2021 to 2026
$4.0M
Professional Development Core for Chicago KUH FORWARDU2CDK129917 · NIDDK · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Nicolae Valentin David · 2021 to 2026
$2.9M
New mechanisms of SERCA2a regulation: role of luminal calciumR01HL151990 · NHLBI · LOYOLA UNIVERSITY CHICAGO · PI ZIMA, ALEKSEY V · 2021 to 2024
$1.7M
Non-hypertensive cardiac disorders in polycystic kidney diseaseR00DK101585 · NIDDK · LOYOLA UNIVERSITY CHICAGO · PI KUO, IVANA Y · 2017 to 2019
$747k
Purchase of a High-Resolution Ultrasound Imaging SystemS10OD028449 · OD · LOYOLA UNIVERSITY CHICAGO · PI ROBIA, SETH L · 2020 to 2020
$551k
NEI NIH HHS R01 EY025799NHLBI NIH HHS R01 HL151990NIDDK NIH HHS R00 DK101585NIDDK NIH HHS TL1 DK132769NIDDK NIH HHS U2C DK129917NIH HHS S10 OD028449
6 · The paper itself

Abstract

Calcium signaling is a critical process required for cellular mechanisms such as cardiomyocyte contraction. The inability of the cell to properly activate or regulate calcium signaling can lead to contractile dysfunction. In isolated cardiomyocytes, calcium signaling has been primarily studied using calcium fluorescent dyes, however these dyes have limited applicability to whole organs. Here, we crossed the Salsa6f mouse which expresses a genetically encoded ratiometric cytosolic calcium indicator with a cardiomyocyte specific inducible cre to temporally-induce expression and studied cytosolic calcium transients in isolated cardiomyocytes and modified Langendorff heart preparations. Isolated cardiomyocytes expressing Salsa6f or Fluo-4AM loaded were compared. We also crossed the Salsa6f mouse with a floxed Polycystin 2 (PC2) mouse to test the feasibility of using the Salsa6f mouse to measure calcium transients in PC2 heterozygous or homozygous knock out mice. Although there are caveats in the applicability of the Salsa6f mouse, there are clear advantages to using the Salsa6f mouse to measure whole heart calcium signals.

Indexed as

CalciumMyocytes, CardiacAnimalsCalcium SignalingFluorescent DyesMiceMyocardial ContractionCalciumFluorescent DyesCalcium handlingCalcium transientsCardiomyocyteGenetically encoded calcium indicators

Identifiers

PMID38537433
PMCPMC11018326

What Socratic holds

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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 Socratic graph.