Evidence map›Paper›PMID 34831374›Full record

ArticleCells2021

MiR 208a Regulates Mitochondrial Biogenesis in Metabolically Challenged Cardiomyocytes.

Naveen Mekala, Jacob Kurdys, Alexis Paige Vicenzi, Leana Rose Weiler, Carmen Avramut, Edwin J Vazquez, Neli Ragina, Mariana G Rosca

Open access · goldAbstract read
In one paragraph

Article in Cells, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Contrasting the genetic architecture of cardiac glutathione against other organs: unveiling a unique tissue-specific locus.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
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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

8 authors at 1 institution in 1 country.

Naveen MekalaDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Jacob KurdysDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Alexis Paige VicenziDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Leana Rose WeilerDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Carmen AvramutDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Edwin J VazquezDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Neli RaginaDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.
Mariana G RoscaDepartment of Foundational Sciences, Central Michigan University College of Medicine, Mount Pleasant, MI 48858, USA.ORCID 0000-0003-3605-9787
Central Michigan University · US

Funding

American Heart Association 18AIREA33990023
6 · The paper itself

Abstract

Metabolic syndrome increases the risk for cardiovascular disease including metabolic cardiomyopathy that may progress to heart failure. The decline in mitochondrial metabolism is considered a critical pathogenic mechanism that drives this progression. Considering its cardiac specificity, we hypothesized that miR 208a regulates the bioenergetic metabolism in human cardiomyocytes exposed to metabolic challenges. We screened in silico for potential miR 208a targets focusing on mitochondrial outcomes, and we found that mRNA species for mediator complex subunit 7, mitochondrial ribosomal protein 28, stanniocalcin 1, and Sortin nexin 10 are rescued by the CRISPR deletion of miR 208a in human SV40 cardiomyocytes exposed to metabolic challenges (high glucose and high albumin-bound palmitate). These mRNAs translate into proteins that are involved in nuclear transcription, mitochondrial translation, mitochondrial integrity, and protein trafficking. MiR 208a suppression prevented the decrease in myosin heavy chain α isoform induced by the metabolic stress suggesting protection against a decrease in cardiac contractility. MiR 208a deficiency opposed the decrease in the mitochondrial biogenesis signaling pathway, mtDNA, mitochondrial markers, and respiratory properties induced by metabolic challenges. The benefit of miR 208a suppression on mitochondrial function was canceled by the reinsertion of miR 208a. In summary, miR 208a regulates mitochondrial biogenesis and function in cardiomyocytes exposed to diabetic conditions. MiR 208a may be a therapeutic target to promote mitochondrial biogenesis in chronic diseases associated with mitochondrial defects.

Indexed as

Organelle BiogenesisAdultBiomarkersDiabetes MellitusHumansMicroRNAsModels, BiologicalMyocytes, CardiacMyosinsProtein IsoformsStress, PhysiologicalBiomarkersMicroRNAsMIRN208 microRNA, humanMyosinsProtein Isoformsbioenergeticscardiomyocytesmetabolic syndromemiR 208amitochondrial biogenesis

Identifiers

PMID34831374
PMCPMC8622724
OpenAlexW3211903973

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.