Evidence map›Paper›PMID 19494234›Full record

ArticleAmerican journal of physiology. Cell physiology2009

Prolactin regulates ZNT2 expression through the JAK2/STAT5 signaling pathway in mammary cells.

Linxi Qian, Veronica Lopez, Young Ah Seo, Shannon L Kelleher

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Cell physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Role of zinc in health and disease.Clinical and experimental medicine · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Remodeling of ZnMetallomics : integrated biometal science · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Zinc-sensitive MRI contrast agent detects differential release of Zn(II) ions from the healthy vs. malignant mouse prostate.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Redistribution of tissue zinc pools during lactation and dyshomeostasis during marginal zinc deficiency in mice.Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements (GMS) · 2015
    Article
  18. Article
  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Linxi QianDepartment of Nutritional Sciences, the Pennsylvania State University, University Park, PA 16802, USA.
Veronica Lopez
Young Ah Seo
Shannon L Kelleher
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 HD-058614-01NICHD NIH HHS R01 HD058614
6 · The paper itself

Abstract

The zinc transporter ZnT2 (SLC30A2) plays an important role in zinc secretion into milk during lactation. The physiological process of mammary gland secretion is regulated through complex integration of multiple lactogenic hormones. Prolactin plays a primary role in this regulation through the activation of various signaling cascades including Jak2/STAT5, mitogen-activated protein kinase (MAPK), p38, and phosphatidylinositol 3-kinase (PI3K). The precise mechanisms that regulate the transfer of specific nutrients such as zinc into milk are not well understood. Herein we report that prolactin increased ZnT2 abundance transcriptionally in cultured mammary epithelial (HC11) cells. To delineate the responsible mechanisms, we first determined that prolactin-mediated ZnT2 induction was inhibited by pretreatment with the Jak2 inhibitor AG490 but not by the MAPK inhibitor PD-98059. Using a luciferase reporter assay, we demonstrated that ZnT2 promoter activity was increased by prolactin treatment, which was subsequently abolished by expression of a dominant-negative STAT5 construct, implicating the Jak2/STAT5 signaling pathway in the transcriptional regulation of ZnT2. Two putative consensus STAT5 binding sequences in the ZnT2 promoter were identified (GAS1:-674 to -665 and GAS2:-377 to -368). Mutagenesis of the proximal GAS2 element resulted in complete abrogation of PRL-induced ZnT2 promoter activity. The promoter incorporating the distal GAS1 mutation was only able to respond to very high PRL concentrations. Results from both the mutagenesis and gel shift assays indicated that a cooperative relationship exists between GAS1 and GAS2 for PRL-induced activation; however, the proximal GAS2 plays a more critical role in STAT5-mediated signal transduction compared with the GAS1 element. Finally, chromosome immunoprecipition assay further confirmed that prolactin activates STAT5 binding to the ZnT2 promoter in vivo. Taken together, these results illustrate that prolactin regulates the transcription of ZnT2 through activation of the Jak2/STAT5 signaling pathway to assist in providing optimal zinc for secretion into milk during lactation.

Indexed as

AnimalsBinding SitesCation Transport ProteinsCell LineEnzyme InhibitorsEpithelial CellsFemaleGene Expression RegulationHumansJanus Kinase 2LactationMammary Glands, AnimalMiceMilkProlactinPromoter Regions, GeneticCation Transport ProteinsEnzyme InhibitorsJanus Kinase 2ProlactinSTAT5 Transcription FactorZincZnt2 protein, mouse

Identifiers

PMID19494234
PMCPMC2724096
OpenAlexW2000638098

What OpenQuestion holds

Textmetadata
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.