Evidence map›Paper›PMID 35260295›Full record

ReviewSeminars in cell & developmental biology2022

Removal of cellular protrusions.

Mayu Inaba, Sharif M Ridwan, Matthew Antel

Abstract readReview
In one paragraph

Review in Seminars in cell & developmental biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. 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

3 authors.

Mayu InabaDepartment of Cell Biology, University of Connecticut Health Center, Farmington, CT 06030, USA. Electronic address: inaba@uchc.edu.
Sharif M RidwanDepartment of Cell Biology, University of Connecticut Health Center, Farmington, CT 06030, USA.
Matthew AntelDepartment of Cell Biology, University of Connecticut Health Center, Farmington, CT 06030, USA.

Funding

Nanotube-mediated regulation of niche-stem cell signalingR35GM128678 · NIGMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Mayu Inaba-Oguro · 2018 to 2026
$3.3M
NIGMS NIH HHS R35 GM128678
6 · The paper itself

Abstract

Cell-cell communications are central to a variety of physiological and pathological processes in multicellular organisms. Cells often rely on cellular protrusions to communicate with one another, which enable highly selective and efficient signaling within complex tissues. Owing to significant improvements in imaging techniques, identification of signaling protrusions has increased in recent years. These protrusions are structurally specialized for signaling and facilitate interactions between cells. Therefore, physical regulation of these structures must be key for the appropriate strength and pattern of signaling outcomes. However, the typical approaches for understanding signaling regulation tend to focus solely on changes in signaling molecules, such as gene expression, protein-protein interaction, and degradation. In this short review, we summarize the studies proposing the removal of different types of signaling protrusions-including cilia, neurites, MT (microtubule based)-nanotubes and microvilli-and discuss their mechanisms and significance in signaling regulation.

Indexed as

Cell CommunicationCell Surface ExtensionsMicrotubulesNeuritesSignal TransductionCiliaEctocytosisMicrotubule-based (MT)-nanotubesNeurite pruningPhagocytosisSignaling protrusionTrogocytosis

Identifiers

PMID35260295
PMCPMC9378436

What OpenQuestion holds

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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.