Evidence map›Paper›PMID 39379155›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2024

Deciphering Peripheral Taste Neuron Diversity: Using Genetic Identity to Bridge Taste Bud Innervation Patterns and Functional Responses.

Lisa C Ohman, Tao Huang, Victori A Unwin, Aditi Singh, Brittany Walters, Zachary D Whiddon, Robin F Krimm

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

Lisa C OhmanDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Tao HuangDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Victori A UnwinDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Aditi SinghDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Brittany WaltersDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Zachary D WhiddonDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Robin F KrimmDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, Kentucky 40202 robin.krimm@louisville.edu.ORCID 0000-0001-5025-3346

Funding

Regulation of taste neuron morphology and functionR01DC007176 · NIDCD · UNIVERSITY OF LOUISVILLE · PI Robin Frances Krimm · 2005 to 2026
$8.1M
Connectivity of periperal taste neuronsF31DC017660 · NIDCD · UNIVERSITY OF LOUISVILLE · PI OHMAN, LISA C · 2018 to 2021
$103k
NIDCD NIH HHS F31 DC017660NIDCD NIH HHS R01 DC007176
6 · The paper itself

Abstract

Peripheral taste neurons exhibit functional, genetic, and morphological diversity, yet understanding how or if these attributes combine into taste neuron types remains unclear. In this study, we used male and female mice to relate taste bud innervation patterns to the function of a subset of proenkephalin-expressing (Penk+) taste neurons. We found that taste arbors (the portion of the axon within the taste bud) stemming from Penk+ neurons displayed diverse branching patterns and lacked stereotypical endings. The range in complexity observed for individual taste arbors from Penk+ neurons mirrored the entire population, suggesting that taste arbor morphologies are not primarily regulated by the neuron type. Notably, the distinguishing feature of arbors from Penk+ neurons was their propensity to come within 110 nm (in apposition with) different types of taste-transducing cells within the taste bud. This finding is contrary to the expectation of genetically defined taste neuron types that functionally represent a single stimulus. Consistently, further investigation of Penk+ neuron function revealed that they are more likely to respond to innately aversive stimuli-sour, bitter, and high salt concentrations-as compared with the full taste population. Penk+ neurons are less likely to respond to nonaversive stimuli-sucrose, umami, and low salt-compared with the full population. Our data support the presence of a genetically defined neuron type in the geniculate ganglion that is responsive to innately aversive stimuli. This implies that genetic expression might categorize peripheral taste neurons into hedonic groups, rather than simply identifying neurons that respond to a single stimulus.

Indexed as

EnkephalinsTasteTaste BudsAnimalsFemaleMaleMiceMice, Inbred C57BLMice, TransgenicProtein PrecursorsEnkephalinspreproenkephalinProtein Precursorsafferentgeniculate gangliongeniculate neuronmorphologytastetongue

Identifiers

PMID39379155
PMCPMC11561867

What Socratic 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 Socratic graph.