Evidence map›Paper›PMID 32132660›Full record

ArticleScientific reports2020

Deletion of metal transporter Zip14 (Slc39a14) produces skeletal muscle wasting, endotoxemia, Mef2c activation and induction of miR-675 and Hspb7.

Jinhee Kim, Tolunay Beker Aydemir, Felix R Jimenez-Rondan, Courtney H Ruggiero, Min-Hyun Kim, Robert J Cousins

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 24 citations in OpenAlex.

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  13. Zinc.Advances in food and nutrition research · 2021
    Review
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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

6 authors at 3 institutions in 1 country.

Jinhee Kim *Food Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA.
Tolunay Beker Aydemir *Food Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA.
Felix R Jimenez-Rondan *Food Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA.
Courtney H RuggieroFood Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA.
Min-Hyun KimFood Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA.
Robert J CousinsFood Science and Human Nutrition Department, Center for Nutritional Sciences, College of Agricultural and Life Sciences, University of Florida, Gainesville, FL, 32611, USA. cousins@ufl.edu.
University of Florida · USCornell University · USRutgers, The State University of New Jersey · US

Funding

Function of Metal Transporter ZIP14 as Regulated by Proinflammatory StimuliR01DK094244 · NIDDK · UNIVERSITY OF FLORIDA · PI COUSINS, ROBERT J · 2011 to 2020
$2.9M
Function of Metal Transporter ZIP14 as Regulated by Proinflammatory StimuliR56DK094244 · NIDDK · UNIVERSITY OF FLORIDA · PI COUSINS, ROBERT J · 2021 to 2021
$152k
NIDDK NIH HHS R01 DK094244NIDDK NIH HHS R56 DK094244
6 · The paper itself

Abstract

Skeletal muscle represents the largest pool of body zinc, however, little is known about muscle zinc homeostasis or muscle-specific zinc functions. Zip14 (Slc39a14) was the most highly expressed zinc transporter in skeletal muscle of mice in response to LPS-induced inflammation. We compared metabolic parameters of skeletal muscle from global Zip14 knockout (KO) and wild-type mice (WT). At basal steady state Zip14 KO mice exhibited a phenotype that included muscle wasting and metabolic endotoxemia. Microarray and qPCR analysis of gastrocnemius muscle RNA revealed that ablation of Zip14 produced increased muscle p-Mef2c, Hspb7 and miR-675-5p expression and increased p38 activation. ChIP assays showed enhanced binding of NF-[Formula: see text] to the Mef2c promoter. In contrast, LPS-induced systemic inflammation enhanced Zip14-dependent zinc uptake by muscle, increased expression of Atrogin1 and MuRF1 and markedly reduced MyoD. These signatures of muscle atrophy and cachexia were not influenced by Zip14 ablation, however. LPS-induced miR-675-3p and -5p expression was Zip14-dependent. Collectively, these results with an integrative model are consistent with a Zip14 function in skeletal muscle at steady state that supports myogenesis through suppression of metabolic endotoxemia and that Zip14 ablation coincides with sustained activity of phosphorylated components of signaling pathways including p-Mef2c, which causes Hspb7-dependent muscle wasting.

Indexed as

EndotoxemiaWasting SyndromeAnimalsCation Transport ProteinsGene DeletionHSP27 Heat-Shock ProteinsMEF2 Transcription FactorsMiceMice, KnockoutMicroRNAsMuscle, SkeletalCation Transport ProteinsHSP27 Heat-Shock ProteinsHSPB7 protein, mouseMef2c protein, mouseMEF2 Transcription FactorsMicroRNAsMIRN675 microRNA, mouseSLC39A14 protein, mouse

Identifiers

PMID32132660
PMCPMC7055249
OpenAlexW3009092542

What OpenQuestion holds

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LicenceCC BY
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.