Evidence map›Paper›PMID 22753477›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Melanoregulin regulates a shedding mechanism that drives melanosome transfer from melanocytes to keratinocytes.

Xufeng S Wu, Andreas Masedunskas, Roberto Weigert, Neal G Copeland, Nancy A Jenkins, John A Hammer

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

51 citing papers in PubMed, 89 citations in OpenAlex.

  1. Article
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  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Removal of cellular protrusions.Seminars in cell & developmental biology · 2022
    Review
  13. RAB3A Regulates Melanin Exocytosis and Transfer Induced by Keratinocyte-Conditioned Medium.JID innovations : skin science from molecules to population health · 2022
    Article
  14. Article
  15. UVR Promotes Keratinocyte Phagocytosis and Skin Pigmentation Through TRPA1 Channels.Clinical, cosmetic and investigational dermatology · 2022
    Article
  16. Article
  17. Review
  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

6 authors at 3 institutions in 1 country.

Xufeng S WuLaboratory of Cell Biology, National Heart, Lung, and Blood Institute, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892, USA. wux@nhlbi.nih.gov
Andreas Masedunskas
Roberto Weigert
Neal G Copeland
Nancy A Jenkins
John A Hammer
National Institutes of Health · USHouston Methodist · USNational Heart Lung and Blood Institute · US

Funding

Structure And Function Of Unconventional Myosins and CARMIL ProteinsZIAHL000514 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI HAMMER, JOHN A · 2009 to 2018
$9.6M
Molecular Mechanisms regulating membrane trafficking in salivary glandsZIADE000717 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI WEIGERT, ROBERTO · 2009 to 2015
$9.2M
6 · The paper itself

Abstract

Mammalian pigmentation is driven by the intercellular transfer of pigment-containing melanosomes from the tips of melanocyte dendrites to surrounding keratinocytes. Tip accumulation of melanosomes requires myosin Va, because melanosomes concentrate in the center of melanocytes from myosin Va-null (dilute) mice. This distribution defect results in inefficient melanosome transfer and a dilution of coat color. Dilute mice that simultaneously lack melanoregulin, the product of the dilute suppressor locus, exhibit a nearly complete restoration of coat color, but, surprisingly, melanosomes remain concentrated in the center of their melanocytes. Here we show that dilute/dsu melanocytes, but not dilute melanocytes, readily transfer the melanosomes concentrated in their center to surrounding keratinocytes in situ. Using time-lapse imaging of WT melanocyte/keratinocyte cocultures in which the plasma membranes of the two cells are marked with different colors, we define an intercellular melanosome transfer pathway that involves the shedding by the melanocyte of melanosome-rich packages, which subsequently are phagocytosed by the keratinocyte. Shedding, which occurs primarily at dendritic tips but also from more central regions, involves adhesion to the keratinocyte, thinning behind the forming package, and apparent self-abscission. Finally, we show that shedding from the cell center is sixfold more frequent in cultured dilute/dsu melanocytes than in dilute melanocytes, consistent with the in situ data. Together, these results explain how dsu restores the coat color of dilute mice without restoring intracellular melanosome distribution, indicate that melanoregulin is a negative regulator of melanosome transfer, and provide insight into the mechanism of intercellular melanosome transfer.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsBiological Transport, ActiveCarrier ProteinsCells, CulturedCoculture TechniquesIntracellular Signaling Peptides and ProteinsKeratinocytesMelanocytesMelanosomesMiceMice, Mutant StrainsMyosin Heavy ChainsMyosin Type VSkin PigmentationAdaptor Proteins, Vesicular TransportCarrier ProteinsIntracellular Signaling Peptides and Proteinsmelanoregulin protein, mouseMyo5a protein, mouseMyosin Heavy ChainsMyosin Type V

Identifiers

PMID22753477
PMCPMC3412008
OpenAlexW2147216612

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.