Evidence map›Paper›PMID 38804679›Full record

ArticleJournal of cell science2024

Immuno-scanning electron microscopy of islet primary cilia.

Sanja Sviben, Alexander J Polino, Isabella L Melena, Jing W Hughes

Abstract read
In one paragraph

Article in Journal of cell science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Pathogenic variants in the polycystin pore helix cause distinct forms of channel dysfunction.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  5. Article
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Sanja SvibenWashington University Center for Cellular Imaging, Washington University School of Medicine, 660 South Euclid Ave, Saint Louis, MO 63110, USA.ORCID 0000-0001-5918-4834
Alexander J PolinoDepartment of Cell Biology and Physiology, Washington University School of Medicine, 660 South Euclid Ave, Saint Louis, MO 63110, USA.ORCID 0000-0003-2601-3638
Isabella L MelenaDepartment of Medicine, Washington University School of Medicine, 660 South Euclid Ave, Saint Louis, MO 63110, USA.ORCID 0000-0001-7894-0682
Jing W HughesDepartment of Cell Biology and Physiology, Washington University School of Medicine, 660 South Euclid Ave, Saint Louis, MO 63110, USA.ORCID 0000-0003-4397-8175

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Irfan J Lodhi · 2013 to 2026
$27.1M
The Human Islet Distribution Coordinating Center (UC4)UC4DK098085 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI EVANS-MOLINA, CARMELLA, NILAND, JOYCE CAROL · 2012 to 2017
$25.6M
TRANSGENICS COREP60DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI SCHAFFER, JEAN E. · 1986 to 2012
$25.2M
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
Primary Cilia in Human T1D PancreasR03DK127748 · NIDDK · WASHINGTON UNIVERSITY · PI HUGHES, JING WANG · 2020 to 2021
$315k
NIDDK NIH HHS DK115795NIDDK NIH HHS K08 DK115795NIDDK NIH HHS P30 DK020579NIDDK NIH HHS P60 DK020579NIDDK NIH HHS R01 DK138974NIDDK NIH HHS R03 DK127748NIDDK NIH HHS UC4 DK098085Washington University School of Medicine
6 · The paper itself

Abstract

The definitive demonstration of protein localization on primary cilia has been a challenge for cilia biologists. Primary cilia are solitary thread-like projections that have a specialized protein composition, but as the ciliary structure overlays the cell membrane and other cell parts, the identity of ciliary proteins are difficult to ascertain by conventional imaging approaches like immunofluorescence microscopy. Surface scanning electron microscopy combined with immunolabeling (immuno-SEM) bypasses some of these indeterminacies by unambiguously showing protein expression in the context of the three-dimensional ultrastructure of the cilium. Here, we apply immuno-SEM to specifically identify proteins on the primary cilia of mouse and human pancreatic islets, including post-translationally modified tubulin, intraflagellar transport (IFT)88, the small GTPase Arl13b, as well as subunits of axonemal dynein. Key parameters in sample preparation, immunolabeling and imaging acquisition are discussed to facilitate similar studies by others in the cilia research community.

Indexed as

CiliaIslets of LangerhansAnimalsHumansMiceMicroscopy, Electron, ScanningAxonemeDyneinImmuno-SEMPancreatic isletPrimary cilia

Identifiers

PMID38804679
PMCPMC11166453

What OpenQuestion 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 OpenQuestion graph.