Evidence map›Paper›PMID 33326005›Full record

ArticleThe Journal of cell biology2021

3D FIB-SEM reconstruction of microtubule-organelle interaction in whole primary mouse β cells.

Andreas Müller, Deborah Schmidt, C Shan Xu, Song Pang, Joyson Verner D'Costa, Susanne Kretschmar, Carla Münster, Thomas Kurth, Florian Jug, Martin Weigert and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of cell biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
13.5field-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

66 citing papers in PubMed, 112 citations in OpenAlex.

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  14. Roles of molecular motors in insulin-secreting beta cells.Current opinion in cell biology · 2025
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  18. Deep mapping of thebioRxiv : the preprint server for biology · 2025
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6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 4 countries.

Andreas MüllerMolecular Diabetology, University Hospital and Faculty of Medicine, Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Deborah SchmidtCenter for Systems Biology Dresden, Dresden, Germany.
C Shan XuJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA.
Song PangJanelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA.
Joyson Verner D'CostaMolecular Diabetology, University Hospital and Faculty of Medicine, Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Susanne KretschmarCenter for Molecular and Cellular Bioengineering, Technology Platform, Technische Universität Dresden, Dresden, Germany.
Carla MünsterMolecular Diabetology, University Hospital and Faculty of Medicine, Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Thomas KurthCenter for Molecular and Cellular Bioengineering, Technology Platform, Technische Universität Dresden, Dresden, Germany.
Florian JugCenter for Systems Biology Dresden, Dresden, Germany.
Martin Weigert *Institute of Bioengineering, School of Life Sciences, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
Harald F Hess *Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA.
Michele Solimena *Molecular Diabetology, University Hospital and Faculty of Medicine, Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Deutsches Diabetes-Zentrum e.V. · DEHoward Hughes Medical Institute · USTechnische Universität Dresden · DECenter for Systems Biology Dresden · DEÉcole Polytechnique Fédérale de Lausanne · CHHuman Technopole · IT

Funding

Howard Hughes Medical Institute
6 · The paper itself

Abstract

Microtubules play a major role in intracellular trafficking of vesicles in endocrine cells. Detailed knowledge of microtubule organization and their relation to other cell constituents is crucial for understanding cell function. However, their role in insulin transport and secretion is under debate. Here, we use FIB-SEM to image islet β cells in their entirety with unprecedented resolution. We reconstruct mitochondria, Golgi apparati, centrioles, insulin secretory granules, and microtubules of seven β cells, and generate a comprehensive spatial map of microtubule-organelle interactions. We find that microtubules form nonradial networks that are predominantly not connected to either centrioles or endomembranes. Microtubule number and length, but not microtubule polymer density, vary with glucose stimulation. Furthermore, insulin secretory granules are enriched near the plasma membrane, where they associate with microtubules. In summary, we provide the first 3D reconstructions of complete microtubule networks in primary mammalian cells together with evidence regarding their importance for insulin secretory granule positioning and thus their supportive role in insulin secretion.

Indexed as

Imaging, Three-DimensionalMicroscopy, Electron, ScanningAnimalsCell MembraneCell NucleusCells, CulturedGlucoseInsulinInsulin-Secreting CellsMiceMice, Inbred C57BLMicrotubulesOrganellesSecretory VesiclesGlucoseInsulin

Identifiers

PMID33326005
PMCPMC7748794
OpenAlexW3112551008

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.