Evidence map›Paper›PMID 39667431›Full record

ArticleMetabolism: clinical and experimental2025

Intravital imaging reveals glucose-dependent cilia movement in pancreatic islets in vivo.

Olha Melnyk, Jeff Kaihao Guo, Zipeng Alex Li, Jeong Hun Jo, Jing W Hughes, Amelia K Linnemann

Abstract read
In one paragraph

Article in Metabolism: clinical and experimental, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

6 authors.

Olha MelnykDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Jeff Kaihao GuoDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA.
Zipeng Alex LiDivision of Endocrinology, Metabolism & Lipid Research, Washington University School of Medicine, St. Louis, MO, USA; Medical Scientist Training Program, Washington University School of Medicine, St. Louis, MO, USA.
Jeong Hun JoDivision of Endocrinology, Metabolism & Lipid Research, Washington University School of Medicine, St. Louis, MO, USA.
Jing W HughesDivision of Endocrinology, Metabolism & Lipid Research, Washington University School of Medicine, St. Louis, MO, USA. Electronic address: jing.hughes@wustl.edu.
Amelia K LinnemannDepartment of Pediatrics, Indiana University School of Medicine, Indianapolis, IN, USA; Center for Diabetes and Metabolic Diseases, Indiana University School of Medicine, Indianapolis, IN, USA. Electronic address: aklinnem@iu.edu.

Funding

Translation CoreP30DK097512 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI Carmella Evans-Molina · 2015 to 2026
$17.4M
Autophagy/antioxidant response coupling in pancreatic beta-cell homeostasis regulationR01DK124380 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI LINNEMANN, AMELIA K · 2021 to 2025
$2.0M
Metabolic signaling of the beta cell primary ciliumR01DK140365 · NIDDK · YALE UNIVERSITY · PI Jing Wang Hughes, Matthew J. Merrins · 2024 to 2026
$1.9M
Paracrine regulation of islet cell function by primary ciliaR01DK138974 · NIDDK · YALE UNIVERSITY · PI Jing Wang Hughes · 2024 to 2026
$1.3M
GLUCAGON REGULATION BY A NOVEL BROWN ADIPOSE FACTORK08DK115795 · NIDDK · WASHINGTON UNIVERSITY · PI HUGHES, JING WANG · 2018 to 2022
$768k
Mechanisms of IL-6 Signaling in Beta-cell Stress ResponseR03DK115990 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI LINNEMANN, AMELIA K · 2018 to 2019
$236k
NIDDK NIH HHS K08 DK115795NIDDK NIH HHS P30 DK097512NIDDK NIH HHS R01 DK124380NIDDK NIH HHS R01 DK138974NIDDK NIH HHS R01 DK140365NIDDK NIH HHS R03 DK115990
6 · The paper itself

Abstract

Pancreatic islet cells harbor primary cilia, small sensory organelles that detect environmental changes to regulate hormone secretion and intercellular communication. While the sensory and signaling capacity of primary cilia are well-appreciated, it is less recognized that these organelles also possess active motility, including in dense multicellular tissues such as the pancreatic islet. In this manuscript, we use transgenic cilia reporter mice and an intravital imaging approach to quantitate primary cilia dynamics as it occurs in live mouse pancreatic islets. We validate this imaging workflow as suitable for studying islet cilia motion in real time in vivo and demonstrate that glucose stimulation corresponds to a change in cilia motility, which may be a physiologic measure of nutrient-dependent fluxes in islet cell function. Complementary ex vivo analysis of isolated islets further demonstrates that metabolic stress in the form of lipotoxicity impairs cilia motility and these effects can be reversed by glucose elevation. These findings suggest that cilia motility is sensitive to metabolic stress and highlight its potential functional role in beta cell adaptation.

Indexed as

CiliaGlucoseIslets of LangerhansMice, TransgenicAnimalsIntravital MicroscopyMaleMiceGlucoseBeta cellCiliaGlucoseIntravital imagingMotility

Identifiers

PMID39667431
PMCPMC11718731

What Socratic holds

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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.