Evidence map›Paper›PMID 34280464›Full record

ArticleThe Journal of investigative dermatology2022

Defining a Role for G-Protein Coupled Receptor/cAMP/CRE-Binding Protein Signaling in Hair Follicle Stem Cell Activation.

Matilde Miranda, Itzetl Avila, Jasmine Esparza, Yulia Shwartz, Ya-Chieh Hsu, Rebecca Berdeaux, William E Lowry

Open access · greenAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2022. 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
3.1field-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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  3. CRISPR-MediatedCells · 2026
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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 3 institutions in 1 country.

Matilde MirandaMolecular Biology Institute, UCLA, Los Angeles, California, USA.
Itzetl AvilaDepartment of Molecular, Cell & Developmental Biology, UCLA, Los Angeles, California, USA.
Jasmine EsparzaDepartment of Molecular, Cell & Developmental Biology, UCLA, Los Angeles, California, USA.
Yulia ShwartzDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts, USA; Harvard Stem Cell Institute, Harvard University, Cambridge, Massachussetts, USA.
Ya-Chieh HsuDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts, USA; Harvard Stem Cell Institute, Harvard University, Cambridge, Massachussetts, USA.
Rebecca BerdeauxDepartment of Integrative Biology and Pharmacology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, Texas, USA.
William E LowryMolecular Biology Institute, UCLA, Los Angeles, California, USA; Department of Molecular, Cell & Developmental Biology, UCLA, Los Angeles, California, USA; Division of Dermatology, David Geffen School of Medicine, UCLA, Los Angeles, California, USA; Broad Center for Regenerative Medicine, UCLA, Los Angeles, California, USA; Jonsson Comprehensive Cancer Center, UCLA, Los Angeles, California, USA. Electronic address: blowry@ucla.edu.
University of California, Los Angeles · USHarvard Stem Cell Institute · USThe University of Texas Health Science Center at Houston · US

Funding

UCLA MSD ProgramR25GM055052 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BARBER, PAUL HENRY, HASSON, TAMA W. · 1996 to 2021
$9.2M
Metabolic Control of Hair Follicle Stem Cell Homeostasis and TumorigenesisR01AR070245 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHRISTOFK, HEATHER, LOWRY, WILLIAM E · 2018 to 2022
$2.1M
NIAMS NIH HHS R01 AR070245NIGMS NIH HHS R25 GM055052
6 · The paper itself

Abstract

Manipulation of adrenergic signaling has been shown experimentally and clinically to affect hair follicle growth. In this study, we provide direct evidence that canonical cAMP/CRE-binding protein signaling through adrenergic receptors can regulate hair follicle stem cell (HFSC) activation and hair cycle. We found that CRE-binding protein activation is regulated through the hair cycle and coincides with HFSC activation. Both isoproterenol and procaterol, agonists of adrenergic receptors, show the capacity to activate the hair cycle in mice. Furthermore, deletion of ADRB2 receptor, which is thought to mediate sympathetic nervous system regulation of HFSCs, was sufficient to block HFSC activation. Downstream, stimulation of adenylyl cyclase with forskolin or inhibition of phosphodiesterase to increase cAMP accumulation or direct application of cAMP was each sufficient to promote HFSC activation and accelerate initiation of hair cycle. Genetic induction of a Designer Receptors Exclusively Activated by Designer Drug allele showed that G-protein coupled receptor/GαS stimulation, specifically in HFSCs, promoted the activation of the hair cycle. Finally, we provide evidence that G-protein coupled receptor/CRE-binding protein signaling can potentially act on HFSCs by promoting glycolytic metabolism, which was previously shown to stimulate HFSC activation. Together, these data provide mechanistic insights into the role of sympathetic innervation on HFSC function.

Indexed as

Activating Transcription Factor 2AnimalsCell DifferentiationCyclic AMPGlycolysisHairHair FollicleIsoproterenolKeratin-15MiceMice, Inbred C57BLMice, KnockoutProcaterolReceptors, Adrenergic, beta-2Receptors, G-Protein-CoupledSignal TransductionActivating Transcription Factor 2ADRB2 protein, mouseCyclic AMPIsoproterenolKeratin-15ProcaterolReceptors, Adrenergic, beta-2Receptors, G-Protein-Coupled

Identifiers

PMID34280464
PMCPMC8989631
OpenAlexW3185082101

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.