Evidence map›Paper›PMID 39330565›Full record

ArticleToxics2024

The Fibrotic Phenotype of Human Precision-Cut Lung Slices Is Maintained after Cryopreservation.

Méry Marimoutou, Vivek Patel, Jae Hun Kim, Niccole Schaible, Jose Alvarez, Joseph Hughes, McKenzie Obermok, Carlos Iván Rodríguez, Thomas Kallarakal, Béla Suki and 3 more

Abstract read
In one paragraph

Article in Toxics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. A human airway-on-a-chip microphysiological system for modeling chlorine gas toxicity.Toxicological sciences : an official journal of the Society of Toxicology · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. 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

13 authors.

Méry MarimoutouInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.
Vivek PatelInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.ORCID 0000-0001-8583-1548
Jae Hun KimMechanobiologix, LLC, Newton, MA 02464, USA.
Niccole SchaibleCenter for Vascular Biology Research, Department of Emergency Medicine, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA.
Jose AlvarezInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.
Joseph HughesInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.
McKenzie ObermokInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.
Carlos Iván RodríguezInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.ORCID 0000-0002-4325-6132
Thomas KallarakalInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.
Béla SukiMechanobiologix, LLC, Newton, MA 02464, USA.
Khalid AminDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55455, USA.
Ramaswamy KrishnanMechanobiologix, LLC, Newton, MA 02464, USA.
Holger Peter BehrsingInstitute for In Vitro Sciences, Inc., Gaithersburg, MD 20878, USA.ORCID 0000-0001-7284-9837

Funding

Screening for inhibitors of allergen-associated airway smooth muscle contractionR21AI151695 · NIAID · BETH ISRAEL DEACONESS MEDICAL CENTER · PI KRISHNAN, RAMASWAMY · 2020 to 2021
$481k
National Institutes of Health National Heart, Lung, and Blood Institute R21 AI151695-02NIAID NIH HHS R21 AI151695
6 · The paper itself

Abstract

Human precision-cut lung slices (hPCLS) prepared from fibrotic lungs recapitulate the pathophysiological hallmarks of fibrosis. These hallmark features can also be induced by treating non-fibrotic hPCLS with a fibrotic cocktail (FC). As a result, the fibrotic and fibrosis-induced hPCLS are rapidly emerging as preferred models for disease modeling and drug discovery. However, current hPCLS models are limited by tissue viability in culture, as they are usually only viable for one week after harvesting. Here, we demonstrate that the fibrotic hPCLS can be cryopreserved, stored for months, and then thawed on demand without loss of hPCLS viability or protein content for 14 days post-thawing. Cryopreservation also preserves the pro-fibrotic potential of non-fibrotic hPCLS. Specifically, when we treated the thawed non-fibrotic hPCLS with an FC, we observed significant pro-fibrotic cytokine secretion and elevated tissue stiffness. These pro-fibrotic changes were inhibited by the small-molecule tyrosine kinase inhibitor, Nintedanib. Taken together, our work indicates that a feasible solution to prolong the pre-clinical utility of fibrotic and fibrosis-induced hPCLS is cryopreservation. We anticipate that cryopreserved hPCLS will serve as an advantageous predictive model for the evaluation of pro-fibrotic pathways during acute and chronic toxicity testing.

Indexed as

cryopreservationex vivofibrosishumanin vitro lung modelsIPFnon-animal testingPCLSstiffness

Identifiers

PMID39330565
PMCPMC11436228

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Registered trials

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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.