Evidence map›Paper›PMID 30758073›Full record

ArticleExperimental dermatology2019

Dissection of Merkel cell formation in hairy and glabrous skin reveals a common requirement for FGFR2-mediated signalling.

Minh Binh Nguyen, Victor Julian Valdes, Idan Cohen, Venu Pothula, Dejian Zhao, Deyou Zheng, Elena Ezhkova

Open access · greenAbstract read
In one paragraph

Article in Experimental dermatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

12 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Development and regeneration of Merkel cells.Current topics in developmental biology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. [Research advances on the function of skin touch receptor Merkel cells].Zhonghua shao shang yu chuang mian xiu fu za zhi · 2022
    Article
  10. Article
  11. Conversion of Sox2-dependent Merkel cell carcinoma to a differentiated neuron-like phenotype by T antigen inhibition.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  12. 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

7 authors at 2 institutions in 2 countries.

Minh Binh NguyenDepartment of Cell, Developmental, and Regenerative Biology, Black Family Stem Cell Institute, The Tisch Cancer Institute, New York City, New York.
Victor Julian ValdesDepartment of Cell, Developmental, and Regenerative Biology, Black Family Stem Cell Institute, The Tisch Cancer Institute, New York City, New York.
Idan CohenDepartment of Cell, Developmental, and Regenerative Biology, Black Family Stem Cell Institute, The Tisch Cancer Institute, New York City, New York.
Venu PothulaDepartment of Cell, Developmental, and Regenerative Biology, Black Family Stem Cell Institute, The Tisch Cancer Institute, New York City, New York.
Dejian ZhaoDepartment of Genetics, Albert Einstein College of Medicine, Bronx, New York.
Deyou ZhengDepartments of Genetics, Neurology, and Neuroscience, Albert Einstein College of Medicine, Bronx, New York.
Elena EzhkovaDepartment of Cell, Developmental, and Regenerative Biology, Black Family Stem Cell Institute, The Tisch Cancer Institute, New York City, New York.ORCID 0000-0003-4154-1615
Tisch Hospital · USAlbert Einstein College of Medicine · US

Funding

Molecular and Cellular Mechanisms in Coronary Artery Development and AnomaliesR01HL133120 · NHLBI · UNIVERSITY OF CHICAGO · PI BIN ZHOU · 2016 to 2026
$4.6M
Toward understanding the molecular mechanisms of Merkel cell fate determinationR01AR063724 · NIAMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI EZHKOVA, ELENA · 2012 to 2021
$4.2M
Cancer Center SupportNHLBI NIH HHS R01 HL133120NIAMS NIH HHS R01 AR063724
6 · The paper itself

Abstract

Merkel cells are mechanosensory cells involved in tactile discrimination. Merkel cells have been primarily studied in the murine back skin, where they are found in specialized structures called touch domes located around primary hair follicles. Yet, little is known about the morphogenesis of Merkel cells in areas of the skin devoid of hair, such as the glabrous paw skin. Here, we describe Merkel cell formation in the glabrous paw skin during embryogenesis. We first found in the glabrous paw skin that Merkel cells were specified at E15.5, 24 hours later, compared to in the back skin. Additionally, by performing lineage-tracing experiments, we found that unlike in the back skin, SOX9(+) cells do not give rise to Merkel cells in the glabrous paw skin. Finally, we compared the transcriptomes of Merkel cells in the back and the glabrous paw skin and showed that they are similar. Genetic and transcriptome studies showed that the formation of Merkel cells in both regions was controlled by similar regulators. Among them was FGFR2, an upstream factor of MAPK signalling that was reported to have a critical function in Merkel cell formation in the back skin. Here, we showed that FGFR2 is also required for Merkel cell development in the glabrous paw skin. Taken together, our results demonstrate that Merkel cells in the murine back skin and glabrous paw skin are similar, and even though their formation is controlled by a common genetic programme, their precursor cells might differ.

Indexed as

Merkel CellsAnimalsFemaleMicePregnancyReceptor, Fibroblast Growth Factor, Type 2SkinTranscriptomeFgfr2 protein, mouseReceptor, Fibroblast Growth Factor, Type 2FGFR2glabrous skinhair follicleMerkel cells

Identifiers

PMID30758073
PMCPMC6488392
OpenAlexW2914129457

What OpenQuestion holds

Textmetadata
LicenceTDM
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.