Evidence map›Paper›PMID 35849202›Full record

ArticleHistochemistry and cell biology2022

Immunolocalization of zinc transporters and metallothioneins reveals links to microvascular morphology and functions.

Hai B Tran, Rachel Jakobczak, Adrian Abdo, Patrick Asare, Paul Reynolds, John Beltrame, Sandra Hodge, Peter Zalewski

Open access · hybridAbstract read
In one paragraph

Article in Histochemistry and cell biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  6. In focus in HCB.Histochemistry and cell biology · 2022
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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 4 institutions in 1 country.

Hai B TranDepartment of Thoracic Medicine, Royal Adelaide Hospital, School of Medicine, University of Adelaide, Adelaide, SA, Australia. haibac.tran@adelaide.edu.au.
Rachel JakobczakTranslational Vascular Function Research Collaborative, Basil Hetzel Institute for Translational Health Research and The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
Adrian AbdoTranslational Vascular Function Research Collaborative, Basil Hetzel Institute for Translational Health Research and The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
Patrick AsareDepartment of Thoracic Medicine, Royal Adelaide Hospital, School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Paul ReynoldsDepartment of Thoracic Medicine, Royal Adelaide Hospital, School of Medicine, University of Adelaide, Adelaide, SA, Australia.
John BeltrameTranslational Vascular Function Research Collaborative, Basil Hetzel Institute for Translational Health Research and The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
Sandra Hodge *Department of Thoracic Medicine, Royal Adelaide Hospital, School of Medicine, University of Adelaide, Adelaide, SA, Australia.
Peter Zalewski *Translational Vascular Function Research Collaborative, Basil Hetzel Institute for Translational Health Research and The Queen Elizabeth Hospital, University of Adelaide, Adelaide, SA, Australia.
University of Adelaide · AUBasil Hetzel Institute · AUQueen Elizabeth Hospital · AURoyal Adelaide Hospital · AU

Funding

National Health and Medical Research Council APP1138917National Health and Medical Research Council APP1147619
6 · The paper itself

Abstract

Zinc homeostasis is vital to immune and other organ system functions, yet over a quarter of the world's population is zinc deficient. Abnormal zinc transport or storage protein expression has been linked to diseases, such as cancer and chronic obstructive pulmonary disorder. Although recent studies indicate a role for zinc regulation in vascular functions and diseases, detailed knowledge of the mechanisms involved remains unknown. This study aimed to assess protein expression and localization of zinc transporters of the SLC39A/ZIP family (ZIPs) and metallothioneins (MTs) in human subcutaneous microvessels and to relate them to morphological features and expression of function-related molecules in the microvasculature. Microvessels in paraffin biopsies of subcutaneous adipose tissues from 14 patients undergoing hernia reconstruction surgery were analysed for 9 ZIPs and 3 MT proteins by MQCM (multifluorescence quantitative confocal microscopy). Zinc regulation proteins detected in human microvasculature included ZIP1, ZIP2, ZIP8, ZIP10, ZIP12, ZIP14 and MT1-3, which showed differential localization among endothelial and smooth muscle cells. ZIP1, ZIP2, ZIP12 and MT3 showed significantly (p < 0.05) increased immunoreactivities, in association with increased microvascular muscularization, and upregulated ET-1, α-SMA and the active form of p38 MAPK (Thr180/Tyr182 phosphorylated, p38 MAPK-P). These findings support roles of the zinc regulation system in microvascular physiology and diseases.

Indexed as

Cation Transport ProteinsCarrier ProteinsHumansMetallothioneinp38 Mitogen-Activated Protein KinasesZincCarrier ProteinsCation Transport ProteinsMetallothioneinp38 Mitogen-Activated Protein KinasesZinczinc-binding proteinMetallothioneinsMultifluorescence quantitative confocal microscopyPulmonary arterial hypertensionSLC39A/ZIPs zinc transportersVascular dysfunctionZIP12

Identifiers

PMID35849202
PMCPMC9630201
OpenAlexW4285728883

What Socratic holds

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LicenceCC BY
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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 Socratic graph.