Evidence map›Paper›PMID 21702047›Full record

ArticleJournal of cellular physiology2012

Mapping the zinc-transporting system in mammary cells: molecular analysis reveals a phenotype-dependent zinc-transporting network during lactation.

Shannon L Kelleher, Vanessa Velasquez, Thomas P Croxford, Nicholas H McCormick, Veronica Lopez, Joshua MacDavid

Abstract read
In one paragraph

Article in Journal of cellular physiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

43 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. 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
  4. Article
  5. Review
  6. Biochemical Markers of Zinc Nutrition.Biological trace element research · 2024
    Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. The role of labile ZnMolecular and cellular biochemistry · 2021
    Review
  16. Review
  17. Remodeling of ZnMetallomics : integrated biometal science · 2020
    Article
  18. Review
  19. Article
  20. Differential expression of zinc transporters accompanies the differentiation of C2C12 myoblasts.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2018
    Article
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 1 institution in 1 country.

Shannon L KelleherDepartment of Nutritional Sciences, The Pennsylvania State University, University Park, Pennsylvania 16802, USA. slk39@psu.edu
Vanessa Velasquez
Thomas P Croxford
Nicholas H McCormick
Veronica Lopez
Joshua MacDavid
Pennsylvania State University · US

Funding

Regulation of Cellular Zn Redistribution: A Role of ZnT2R01HD058614 · NICHD · PENNSYLVANIA STATE UNIVERSITY, THE · PI KELLEHER, SHANNON L · 2008 to 2012
$1.4M
NICHD NIH HHS R01 HD058614NICHD NIH HHS R01HD058614
6 · The paper itself

Abstract

The mammary epithelial cell transitions from a non-secreting to a terminally differentiated, secreting cell during lactation. Zinc (Zn) is a key modulator of phenotypic transition as it regulates over 300 biological functions including transcription, translation, energy transformation, intracellular signaling, and apoptosis. In addition, Zn must be redirected from normal cellular functions into the secretory compartment, as many components of the secretory system are Zn-dependent and an extraordinary amount of Zn is secreted (1-3 mg Zn/day) into milk. Herein, we utilized a "systems biology" approach of genomic and proteomic profiling to explore mechanisms through which Zn is reallocated during phenotype transition in the lactating mammary gland from mice and cultured mammary cells. Nine Zn transporters play key roles in Zn redistribution within the network during lactation. Protein abundance of six Zip (Zip3, Zip5, Zip7, Zip8, Zip10, Zip11) and three ZnT (ZnT2, ZnT4, ZnT9) proteins was expanded >2-fold during lactation, which was not necessarily reflected by changes in mRNA expression. Our data suggest that Zip5, Zip8, and Zip10 may be key to Zn acquisition from maternal circulation, while multiple Zip proteins reuptake Zn from milk. Confocal microscopy of cultured mammary cells identified the Golgi apparatus (modulated in part by ZnT5, Zip7, and Zip11) and the late endosomal compartment (modulated in part by ZnT2 and Zip3) as key intracellular compartments through which Zn is reallocated during lactation. These results provide an important framework for understanding the "Zn-transporting network" through which mammary gland Zn pools are redistributed and secreted into milk.

Indexed as

AnimalsCarrier ProteinsEpithelial CellsFemaleImmunohistochemistryLactationMammary Glands, AnimalMetabolic Networks and PathwaysMiceMice, Inbred C57BLMilkModels, BiologicalPhenotypePregnancyRNA, MessengerZincCarrier ProteinsRNA, MessengerZinczinc-binding protein

Identifiers

PMID21702047
PMCPMC3207005
OpenAlexW2097040123

What OpenQuestion holds

Textmetadata
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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.