Evidence map›Paper›PMID 41998068›Full record

ArticleScientific reports2026

Real-time snapping dynamics and nanoscale thickness profiling of salmon keratocyte tunneling nanotubes using partially coherent quantitative phase microscopy.

Bilal M Afzal, Marie K Mikkelborg, Dhivya B Thiyagarajan, Deanna L Wolfson, Balpreet S Ahluwalia, Roy A Dalmo, Azeem Ahmad

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Bilal M AfzalThe Norwegian College of Fishery Science, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Marie K MikkelborgThe Norwegian College of Fishery Science, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Dhivya B ThiyagarajanThe Norwegian College of Fishery Science, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Deanna L WolfsonDepartment of Physics and Technology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Balpreet S AhluwaliaDepartment of Physics and Technology, UiT The Arctic University of Norway, 9037, Tromsø, Norway.
Roy A DalmoThe Norwegian College of Fishery Science, UiT The Arctic University of Norway, 9037, Tromsø, Norway. roy.dalmo@uit.no.
Azeem AhmadDepartment of Physics and Technology, UiT The Arctic University of Norway, 9037, Tromsø, Norway. azeem.ahmad@uit.no.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fish skin epithelial cells, known as keratocytes, are highly migratory and exhibit distinctive morphological features, including elongated membrane protrusions called tunneling nanotubes (TNTs). In other cell types, TNTs have been reported to facilitate the intercellular transfer of various cellular cargo. Beyond cargo transport, these structures are also implicated in mediating intercellular signaling. Owing to their extremely small heights, often as low as 100 nm or less, reliable characterization of their morphology and dynamics necessitates the use of a highly sensitive quantitative phase microscopy technique. In this study, a partially spatially coherent quantitative phase microscopy (QPM) system was utilized, providing extremely high spatial sensitivity to track changes in TNT height over time, particularly during the snapping process. A five-frame phase-shifting technique was employed to recover high-resolution phase maps of the TNTs. Observations indicate that TNT height typically ranges from 100 to 900 nm. Additionally, the average height-to-width ratio indicates that the TNTs exhibit a more flattened rather than cylindrical geometry. Further, during the imaging period, diverse behaviors were observed: some TNTs remained intact and maintained structural integrity for the entire duration of the recording, whereas others exhibited rupture. Beyond morphological characterization, this work may open new avenues for understanding TNT’s potential role in the transfer of intracellular cargo, paving the way for future investigations into cellular communication mechanisms.

Identifiers

PMID41998068
PMCPMC13247071

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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.