Evidence map›Paper›PMID 30996124›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Tiling and somatotopic alignment of mammalian low-threshold mechanoreceptors.

Emily D Kuehn, Shan Meltzer, Victoria E Abraira, Cheng-Ying Ho, David D Ginty

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.1field-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

34 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Anatomical Characteristics of Tongue-Innervating Mechanoreceptors.The Journal of comparative neurology · 2026
    Article
  3. Article
  4. Spinal circuits encode a map of the trunk to control skin twitches.bioRxiv : the preprint server for biology · 2026
    Article
  5. Spinal Processing of Spatiotemporally Diverse Tactile Stimuli: Computational Insights into Allodynia and Spinal Cord Stimulation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. The Role of Protocadherin γ in Adult Sensory Neurons and Skin Reinnervation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

5 authors at 3 institutions in 1 country.

Emily D KuehnDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115.
Shan MeltzerDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115.
Victoria E AbrairaDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115.
Cheng-Ying HoSolomon H. Snyder Department of Neuroscience, The Johns Hopkins University School of Medicine, Baltimore, MD 21205.
David D GintyDepartment of Neurobiology, Harvard Medical School, Boston, MA 02115; david_ginty@hms.harvard.edu.
Harvard University · USJohns Hopkins Medicine · USHoward Hughes Medical Institute · US

Funding

Elucidating Cutaneous Mechanosensory Circuits, from Development to DiseaseR35NS097344 · NINDS · HARVARD MEDICAL SCHOOL · PI GINTY, DAVID D · 2016 to 2023
$6.8M
The role of skin BDNF in the maintenance of the cutaneous mechanosensory nervous systemK08NS102468 · NINDS · UNIVERSITY OF MARYLAND BALTIMORE · PI HO, CHENG-YING · 2018 to 2022
$1.0M
The Organization and Molecular Mechanisms of Touch Circuits During DevelopmentF32NS108507 · NINDS · HARVARD MEDICAL SCHOOL · PI MELTZER, SHAN · 2018 to 2018
$36k
NINDS NIH HHS F32 NS108507NINDS NIH HHS K08 NS102468NINDS NIH HHS R35 NS097344
6 · The paper itself

Abstract

Innocuous mechanical stimuli acting on the skin are detected by sensory neurons, known as low-threshold mechanoreceptors (LTMRs). LTMRs are classified based on their response properties, action potential conduction velocity, rate of adaptation to static indentation of the skin, and terminal anatomy. Here, we report organizational properties of the cutaneous and central axonal projections of the five principal hairy skin LTMR subtypes. We find that axons of neurons within a particular LTMR class are largely nonoverlapping with respect to their cutaneous end organs (e.g., hair follicles), with Aβ rapidly adapting-LTMRs being the sole exception. Individual neurons of each LTMR class are mostly nonoverlapping with respect to their associated hair follicles, with the notable exception of C-LTMRs, which exhibit multiple branches that redundantly innervate individual hair follicles. In the spinal cord, LTMR central projections exhibit rostrocaudal elongation and mediolateral compression, compared with their cutaneous innervation patterns, and these central projections also exhibit a fine degree of homotypic topographic adjacency. These findings thus reveal homotypic tiling of LTMR subtype axonal projections in hairy skin and a remarkable degree of spatial precision of spinal cord axonal termination patterns, suggesting a somatotopically precise tactile encoding capability of the mechanosensory dorsal horn.

Indexed as

AnimalsAxonsHumansMammalsMechanoreceptorsMiceSkinSkin Physiological PhenomenaSpinal CordTouchmechanosensorysomatosensationsomatotopytiling

Identifiers

PMID30996124
PMCPMC6511030
OpenAlexW2937866010

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.