Evidence map›Paper›PMID 35426185›Full record

ArticleTraffic (Copenhagen, Denmark)2022

Melanocore uptake by keratinocytes occurs through phagocytosis and involves protease-activated receptor-2 internalization.

Hugo Moreiras, Liliana Bento-Lopes, Matilde V Neto, Cristina Escrevente, Luís C Cabaço, Michael J Hall, José S Ramalho, Miguel C Seabra, Duarte C Barral

Open access · bronzeAbstract read
In one paragraph

Article in Traffic (Copenhagen, Denmark), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. A Narrative Review of the Multi-Target Mechanisms of Glabridin in Skin Lightening.Clinical, cosmetic and investigational dermatology · 2026
    Review
  5. Article
  6. Article
  7. Disrupting melanin transfer: innovative strategy for anti-pigmentation drug discovery.Journal of enzyme inhibition and medicinal chemistry · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. EGF-Induced Macropinocytosis Promotes NAV1-Dependent Internalization of Occludin in Keratinocytes.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  14. Implication of Immunobiological Function of Melanocytes in Dermatology.Clinical reviews in allergy & immunology · 2025
    Review
  15. Article
  16. Review
  17. Review
  18. The journey from melanocytes to melanoma.Nature reviews. Cancer · 2023
    Review
  19. Review
  20. Biology of melanocytes in mammals.Frontiers in cell and developmental biology · 2023
    Review
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

9 authors at 1 institution in 1 country.

Hugo MoreirasCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0003-0984-7921
Liliana Bento-LopesCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0002-6893-610X
Matilde V NetoCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.
Cristina EscreventeCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0002-2183-3947
Luís C CabaçoCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0003-0976-1781
Michael J HallCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0002-1579-1488
José S RamalhoCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0002-1927-164X
Miguel C SeabraCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0002-6404-4892
Duarte C BarralCEDOC-Chronic Diseases Research Center, NOVA Medical School (NMS), Faculdade de Ciências Médicas, Universidade NOVA de Lisboa, Lisbon, Portugal.ORCID 0000-0001-8867-2407
Universidade Nova de Lisboa · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the skin epidermis, melanin is produced and stored within melanosomes in melanocytes, and then transferred to keratinocytes. Different models have been proposed to explain the melanin transfer mechanism, which differ essentially in how melanin is transferred-either in a membrane-bound melanosome or as a melanosome core, that is, melanocore. Here, we investigated the endocytic route followed by melanocores and melanosomes during internalization by keratinocytes, by comparing the uptake of melanocores isolated from the supernatant of melanocyte cultures, with melanosomes isolated from melanocytes. We show that inhibition of actin dynamics impairs the uptake of both melanocores and melanosomes. Moreover, depletion of critical proteins involved in actin-dependent uptake mechanisms, namely Rac1, CtBP1/BARS, Cdc42 or RhoA, together with inhibition of Rac1-dependent signaling pathways or macropinocytosis suggest that melanocores are internalized by phagocytosis, whereas melanosomes are internalized by macropinocytosis. Interestingly, we found that Rac1, Cdc42 and RhoA are differently activated by melanocore or melanosome stimulation, supporting the existence of two distinct routes of melanin internalization. Furthermore, we show that melanocore uptake induces protease-activated receptor-2 (PAR-2) internalization by keratinocytes to a higher extent than melanosomes. Because skin pigmentation was shown to be regulated by PAR-2 activation, our results further support the melanocore-based mechanism of melanin transfer and further refine this model, which can now be described as coupled melanocore exo/phagocytosis.

Indexed as

MelaninsReceptor, PAR-2ActinsKeratinocytesMelanocytesMelanosomesPhagocytosisActinsMelaninsReceptor, PAR-2macropinocytosismelanocoremelanosomesphagocytosisprotease-activated receptor-2

Identifiers

PMID35426185
PMCPMC9543991
OpenAlexW4223898209

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.