Evidence map›Paper›PMID 38366037›Full record

ReviewNature reviews. Molecular cell biology2024

Emerging mechanistic understanding of cilia function in cellular signalling.

Keren I Hilgendorf, Benjamin R Myers, Jeremy F Reiter

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Molecular cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 106 papers.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed
72.6field-weighted citation impact, top 1% 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

106 citing papers in PubMed, 134 citations in OpenAlex.

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46 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 1 country.

Keren I HilgendorfDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA. keren.hilgendorf@biochem.utah.edu.ORCID http://orcid.org/0000-0001-8377-8384
Benjamin R MyersDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, UT, USA. benjamin.myers@hci.utah.edu.ORCID http://orcid.org/0000-0003-0975-539X
Jeremy F ReiterDepartment of Biochemistry and Biophysics, Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA, USA. jeremy.reiter@ucsf.edu.
University of Utah · USUniversity of California, San Francisco · US

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Clay F. Semenkovich · 2013 to 2026
$27.1M
Hedgehog signaling at the cell's antenna: Smoothened and the primary ciliumR01AR054396 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Jeremy F Reiter · 2007 to 2026
$9.0M
Ciliary signaling mechanisms regulating white adipose tissue expansionR01DK133455 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Keren Hilgendorf · 2022 to 2026
$1.9M
NIAMS NIH HHS R01 AR054396NIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK133455
6 · The paper itself

Abstract

Primary cilia are solitary, immotile sensory organelles present on most cells in the body that participate broadly in human health, physiology and disease. Cilia generate a unique environment for signal transduction with tight control of protein, lipid and second messenger concentrations within a relatively small compartment, enabling reception, transmission and integration of biological information. In this Review, we discuss how cilia function as signalling hubs in cell-cell communication using three signalling pathways as examples: ciliary G-protein-coupled receptors (GPCRs), the Hedgehog (Hh) pathway and polycystin ion channels. We review how defects in these ciliary signalling pathways lead to a heterogeneous group of conditions known as 'ciliopathies', including metabolic syndromes, birth defects and polycystic kidney disease. Emerging understanding of these pathways' transduction mechanisms reveals common themes between these cilia-based signalling pathways that may apply to other pathways as well. These mechanistic insights reveal how cilia orchestrate normal and pathophysiological signalling outputs broadly throughout human biology.

Indexed as

CiliaHedgehog ProteinsSignal TransductionAnimalsCell CommunicationCiliopathiesHumansReceptors, G-Protein-CoupledTRPP Cation ChannelsHedgehog ProteinsReceptors, G-Protein-CoupledTRPP Cation Channels

Identifiers

PMID38366037
PMCPMC11199107
OpenAlexW4391884040

What Socratic 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 Socratic graph.