Evidence map›Paper›PMID 33485965›Full record

ReviewThe Journal of biological chemistry

Zinc transporters and their functional integration in mammalian cells.

Taiho Kambe, Kathryn M Taylor, Dax Fu

Open access · goldAbstract readReview
In one paragraph

Review in The Journal of biological chemistry. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 116 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
116citing papers in PubMed, 1 pooled it
21.2field-weighted citation impact, top 1% 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

116 citing papers in PubMed, 1 synthesis or guideline pooled it, 220 citations in OpenAlex.

  1. Pooled it
  2. ZIP1 Is a Critical DNA Damage-Responsive Zinc Transporter Induced by Bleomycin via the TNFα-NF-κB Pathway.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  3. Ion-Driven Regulation of CaAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Substrate selectivity of human histidine methyltransferase METTL9.Protein science : a publication of the Protein Society · 2026
    Article
  12. Article
  13. An emerging role for synaptic ZnPharmacology & therapeutics · 2026
    Review
  14. Article
  15. ZIP3 is essential for the encephalitogenic function of pTh17 cells by regulating intracellular zinc levels.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2026
    Article
  16. Article
  17. Vitamin D and Mineral Ion Regulation.Advances in experimental medicine and biology · 2026
    Review
  18. Article
  19. Article
  20. Article

56 more citing papers are in PubMed but not listed here.

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

3 authors at 3 institutions in 3 countries.

Taiho KambeDivision of Integrated Life Science, Graduate School of Biostudies, Kyoto University, Kyoto, Japan.
Kathryn M TaylorSchool of Pharmacy and Pharmaceutical Sciences, Cardiff University, Cardiff, United Kingdom.
Dax FuDepartment of Physiology, Johns Hopkins School of Medicine, Johns Hopkins University, Baltimore, Maryland, USA. Electronic address: dfu3@jhmi.edu.
Cardiff University · GBJohns Hopkins University · USKyoto University · JP

Funding

Molecular functions of human zinc transporter-8 in pancreatic beta cellsR01DK125746 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI FU, DAX · 2021 to 2024
$2.0M
Autoantibodies directed to islet cell surface antigens and their pathologic roles in type-1 diabetesR56DK123435 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI FU, DAX, YU, LIPING · 2020 to 2020
$164k
NIDDK NIH HHS R01 DK125746NIDDK NIH HHS R56 DK123435
6 · The paper itself

Abstract

Zinc is a ubiquitous biological metal in all living organisms. The spatiotemporal zinc dynamics in cells provide crucial cellular signaling opportunities, but also challenges for intracellular zinc homeostasis with broad disease implications. Zinc transporters play a central role in regulating cellular zinc balance and subcellular zinc distributions. The discoveries of two complementary families of mammalian zinc transporters (ZnTs and ZIPs) in the mid-1990s spurred much speculation on their metal selectivity and cellular functions. After two decades of research, we have arrived at a biochemical description of zinc transport. However, in vitro functions are fundamentally different from those in living cells, where mammalian zinc transporters are directed to specific subcellular locations, engaged in dedicated macromolecular machineries, and connected with diverse cellular processes. Hence, the molecular functions of individual zinc transporters are reshaped and deeply integrated in cells to promote the utilization of zinc chemistry to perform enzymatic reactions, tune cellular responsiveness to pathophysiologic signals, and safeguard cellular homeostasis. At present, the underlying mechanisms driving the functional integration of mammalian zinc transporters are largely unknown. This knowledge gap has motivated a shift of the research focus from in vitro studies of purified zinc transporters to in cell studies of mammalian zinc transporters in the context of their subcellular locations and protein interactions. In this review, we will outline how knowledge of zinc transporters has been accumulated from in-test-tube to in-cell studies, highlighting new insights and paradigm shifts in our understanding of the molecular and cellular basis of mammalian zinc transporter functions.

Indexed as

Amino Acid SequenceAnimalsCation Transport ProteinsHomeostasisHumansIon TransportZincCation Transport ProteinsZincendoplasmic reticulum stress (ER stress)enzyme processingprotein–protein interactionproteomicssignal transductiontransportertransport metalzinc

Identifiers

PMID33485965
PMCPMC7949119
OpenAlexW3124535662

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.