Evidence map›Paper›PMID 34783306›Full record

ArticleeLife2021

Microtubules regulate pancreatic β-cell heterogeneity via spatiotemporal control of insulin secretion hot spots.

Kathryn P Trogden, Justin Lee, Kai M Bracey, Kung-Hsien Ho, Hudson McKinney, Xiaodong Zhu, Goker Arpag, Thomas G Folland, Anna B Osipovich, Mark A Magnuson and 4 more

Abstract read
In one paragraph

Article in eLife, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Roles of molecular motors in insulin-secreting beta cells.Current opinion in cell biology · 2025
    Review
  6. Article
  7. Epitranscriptomic sculpting: the role of mMedical oncology (Northwood, London, England) · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Insulin secretion hot spots in pancreatic β cells as secreting adhesions.Frontiers in cell and developmental biology · 2023
    Article
  19. Review
  20. 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

14 authors.

Kathryn P TrogdenDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.ORCID 0000-0003-3288-3859
Justin Lee *Department of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Kai M Bracey *Department of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Kung-Hsien Ho *Department of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Hudson McKinney *Department of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Xiaodong ZhuDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Goker ArpagDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.ORCID 0000-0002-6893-2678
Thomas G FollandDepartment of Mechanical Engineering, Vanderbilt University, Nashville, United States.
Anna B OsipovichDepartment of Molecular Physiology and Biophysics, Vanderbilt University, Nashville, United States.
Mark A MagnusonDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
Marija ZanicDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.ORCID 0000-0002-5127-5819
Guoqiang GuDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.
William R HolmesDepartment of Physics and Astronomy, Vanderbilt University, Nashville, United States.
Irina KaverinaDepartment of Cell and Developmental Biology and Program in Developmental Biology, Vanderbilt University, Nashville, United States.ORCID 0000-0002-4002-8599

Funding

Translational Research in Endocrinology And Diabetes (TREAD)T32DK007061 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Sarah S Jaser, KEVIN D NISWENDER · 1986 to 2026
$8.0M
Microtubule Regulation of Pancreatic Beta Cell Function and DiabetesR01DK106228 · NIDDK · VANDERBILT UNIVERSITY · PI Guoqiang Gu, William Holmes · 2016 to 2026
$6.4M
Biophysical Principles of Microtubule DynamicsR35GM119552 · NIGMS · VANDERBILT UNIVERSITY · PI Marija Zanic · 2016 to 2026
$4.4M
The Mechanisms of Islet Cell Specification and DifferentiationR01DK065949 · NIDDK · VANDERBILT UNIVERSITY · PI GU, GUOQIANG · 2004 to 2017
$4.4M
Dynamic architecture of microtubule networksR35GM127098 · NIGMS · VANDERBILT UNIVERSITY · PI Irina Kaverina · 2018 to 2026
$4.1M
The DNA methylome-based regulation of functional beta-cell massR01DK125696 · NIDDK · VANDERBILT UNIVERSITY · PI Guoqiang Gu · 2020 to 2026
$3.4M
The Role of Microtubule Sliding in Regulation of Insulin SecretionF31DK122650 · NIDDK · VANDERBILT UNIVERSITY · PI BRACEY, KAI M. · 2019 to 2021
$89k
Regulation and Function of Golgi-derived Microtubules in Pancreatic Beta-cell Physiology and DiabetesF32DK117529 · NIDDK · VANDERBILT UNIVERSITY · PI TROGDEN, KATHRYN · 2018 to 2018
$61k
NIDDK NIH HHS F31 DK122650NIDDK NIH HHS F32 DK117529NIDDK NIH HHS R01 DK065949NIDDK NIH HHS R01 DK106228NIDDK NIH HHS R01 DK125696NIDDK NIH HHS T32 DK007061NIGMS NIH HHS R35 GM119552NIGMS NIH HHS R35 GM127098
6 · The paper itself

Abstract

Heterogeneity of glucose-stimulated insulin secretion (GSIS) in pancreatic islets is physiologically important but poorly understood. Here, we utilize mouse islets to determine how microtubules (MTs) affect secretion toward the vascular extracellular matrix at single cell and subcellular levels. Our data indicate that MT stability in the β-cell population is heterogenous, and that GSIS is suppressed in cells with highly stable MTs. Consistently, MT hyper-stabilization prevents, and MT depolymerization promotes the capacity of single β-cell for GSIS. Analysis of spatiotemporal patterns of secretion events shows that MT depolymerization activates otherwise dormant β-cells via initiation of secretion clusters (hot spots). MT depolymerization also enhances secretion from individual cells, introducing both additional clusters and scattered events. Interestingly, without MTs, the timing of clustered secretion is dysregulated, extending the first phase of GSIS and causing oversecretion. In contrast, glucose-induced Ca

Indexed as

Insulin SecretionAnimalsFemaleInsulinInsulin-Secreting CellsMaleMiceMicrotubulesSpatio-Temporal AnalysisInsulinbiphasic secretioncell biologycomputational cluster analysisdiabetesmedicinemicrotubule dynamicsmicrotubule stabilitymousestimulus-secretion coupling

Identifiers

PMID34783306
PMCPMC8635970

What Socratic 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 Socratic graph.