Evidence map›Paper›PMID 39088574›Full record

ArticlePloS one2024

Intravital two-photon microscopy of the native mouse thymus.

Negar Seyedhassantehrani, Christian S Burns, Ruth Verrinder, Victoria Okafor, Nastaran Abbasizadeh, Joel A Spencer

Abstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. TWINKLE: An open-source two-photon microscope for teaching and research.bioRxiv : the preprint server for biology · 2025
    Article
  3. 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

6 authors.

Negar SeyedhassantehraniQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, California, United States of America.
Christian S BurnsQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, California, United States of America.ORCID 0000-0003-2090-0252
Ruth VerrinderNSF-CREST Center for Cellular and Biomolecular Machines, University of California Merced, Merced, California, United States of America.ORCID 0000-0002-8297-7856
Victoria OkaforNSF-CREST Center for Cellular and Biomolecular Machines, University of California Merced, Merced, California, United States of America.
Nastaran AbbasizadehQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, California, United States of America.
Joel A SpencerQuantitative and Systems Biology Graduate Program, University of California Merced, Merced, California, United States of America.ORCID 0000-0002-4013-8763

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The thymus, a key organ in the adaptive immune system, is sensitive to a variety of insults including cytotoxic preconditioning, which leads to atrophy, compression of the blood vascular system, and alterations in hemodynamics. Although the thymus has innate regenerative capabilities, the production of T cells relies on the trafficking of lymphoid progenitors from the bone marrow through the altered thymic blood vascular system. Our understanding of thymic blood vascular hemodynamics is limited due to technical challenges associated with accessing the native thymus in live mice. To overcome this challenge, we developed an intravital two-photon imaging method to visualize the native thymus in vivo and investigated functional changes to the vascular system following sublethal irradiation. We quantified blood flow velocity and shear rate in cortical blood vessels and identified a subtle but significant increase in vessel leakage and diameter ~24 hrs post-sublethal irradiation. Ex vivo whole organ imaging of optically cleared thymus lobes confirmed a disruption of the thymus vascular structure, resulting in an increase in blood vessel diameter and vessel area, and concurrent thymic atrophy. This novel two-photon intravital imaging method enables a new paradigm for directly investigating the thymic microenvironment in vivo.

Indexed as

Intravital MicroscopyThymus GlandAnimalsHemodynamicsMiceMice, Inbred C57BLMicroscopy, Fluorescence, Multiphoton

Identifiers

PMID39088574
PMCPMC11293686

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.