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  1. Article ; Online: Viral airway injury promotes cell engraftment in an in vitro model of cystic fibrosis cell therapy.

    Lee, Rhianna E / Mascenik, Teresa M / Major, Sidra C / Galiger, Jacob R / Bulik-Sullivan, Emily / Siesser, Priscila F / Lewis, Catherine A / Bear, James E / Le Suer, Jake A / Hawkins, Finn J / Pickles, Raymond J / Randell, Scott H

    American journal of physiology. Lung cellular and molecular physiology

    2023  Volume 326, Issue 3, Page(s) L226–L238

    Abstract: Cell therapy is a potential treatment for cystic fibrosis (CF). However, cell engraftment into the airway epithelium is challenging. Here, we model cell engraftment in vitro using the air-liquid interface (ALI) culture system by injuring well- ... ...

    Abstract Cell therapy is a potential treatment for cystic fibrosis (CF). However, cell engraftment into the airway epithelium is challenging. Here, we model cell engraftment in vitro using the air-liquid interface (ALI) culture system by injuring well-differentiated CF ALI cultures and delivering non-CF cells at the time of peak injury. Engraftment efficiency was quantified by measuring chimerism by droplet digital PCR and functional ion transport in Ussing chambers. Using this model, we found that human bronchial epithelial cells (HBECs) engraft more efficiently when they are cultured by conditionally reprogrammed cell (CRC) culture methods. Cell engraftment into the airway epithelium requires airway injury, but the extent of injury needed is unknown. We compared three injury models and determined that severe injury with partial epithelial denudation facilitates long-term cell engraftment and functional CFTR recovery up to 20% of wildtype function. The airway epithelium promptly regenerates in response to injury, creating competition for space and posing a barrier to effective engraftment. We examined competition dynamics by time-lapse confocal imaging and found that delivered cells accelerate airway regeneration by incorporating into the epithelium. Irradiating the repairing epithelium granted engrafting cells a competitive advantage by diminishing resident stem cell proliferation. Intentionally, causing severe injury to the lungs of people with CF would be dangerous. However, naturally occurring events like viral infection can induce similar epithelial damage with patches of denuded epithelium. We found that viral preconditioning promoted effective engraftment of cells primed for viral resistance.
    MeSH term(s) Humans ; Cystic Fibrosis/therapy ; Cystic Fibrosis Transmembrane Conductance Regulator/genetics ; Epithelium ; Epithelial Cells ; Cell- and Tissue-Based Therapy ; Virus Diseases ; Cells, Cultured
    Chemical Substances Cystic Fibrosis Transmembrane Conductance Regulator (126880-72-6)
    Language English
    Publishing date 2023-12-27
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1013184-x
    ISSN 1522-1504 ; 1040-0605
    ISSN (online) 1522-1504
    ISSN 1040-0605
    DOI 10.1152/ajplung.00421.2022
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Prolonged airway explant culture enables study of health, disease, and viral pathogenesis.

    Lee-Ferris, Rhianna E / Okuda, Kenichi / Galiger, Jacob R / Schworer, Stephen A / Rogers, Troy D / Dang, Hong / Gilmore, Rodney / Edwards, Caitlin / Nakano, Satoko / Cawley, Anne M / Pickles, Raymond J / Gallant, Samuel C / Crisci, Elisa / Rivier, Lauraine / Hagood, James S / O'Neal, Wanda K / Baric, Ralph S / Grubb, Barbara R / Boucher, Richard C /
    Randell, Scott H

    bioRxiv : the preprint server for biology

    2024  

    Abstract: In vitro models play a major role in studying airway physiology and disease. However, the native lung's complex tissue architecture and non-epithelial cell lineages are not preserved in these models. Ex vivo tissue models could overcome in vitro ... ...

    Abstract In vitro models play a major role in studying airway physiology and disease. However, the native lung's complex tissue architecture and non-epithelial cell lineages are not preserved in these models. Ex vivo tissue models could overcome in vitro limitations, but methods for long-term maintenance of ex vivo tissue has not been established. We describe methods to culture human large airway explants, small airway explants, and precision-cut lung slices for at least 14 days. Human airway explants recapitulate genotype-specific electrophysiology, characteristic epithelial, endothelial, stromal and immune cell populations, and model viral infection after 14 days in culture. These methods also maintain mouse, rabbit, and pig tracheal explants. Notably, intact airway tissue can be cryopreserved, thawed, and used to generate explants with recovery of function 14 days post-thaw. These studies highlight the broad applications of airway tissue explants and their use as translational intermediates between in vitro and in vivo studies.
    Language English
    Publishing date 2024-02-05
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2024.02.03.578756
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Prolonged airway explant culture enables study of health, disease, and viral pathogenesis

    Lee-Ferris, Rhianna E / Okuda, Kenichi / Galiger, Jacob R / Schworer, Stephen A / Rogers, Troy D / Dang, Hong / Gilmore, Rodney / Edwards, Caitlin / Nakano, Satoko / Cawley, Anne M. / Pickles, Raymond J / Gallant, Samuel C / Crisci, Elisa / Rivier, Lauraine / Hagood, James S / O’Neal, Wanda K / Baric, Ralph S / Grubb, Barbara R / Boucher, Richard C /
    Randell, Scott H

    bioRxiv

    Abstract: In vitro models play a major role in studying airway physiology and disease. However, the native lungs complex tissue architecture and non-epithelial cell lineages are not preserved in these models. Ex vivo tissue models could overcome in vitro ... ...

    Abstract In vitro models play a major role in studying airway physiology and disease. However, the native lungs complex tissue architecture and non-epithelial cell lineages are not preserved in these models. Ex vivo tissue models could overcome in vitro limitations, but methods for long-term maintenance of ex vivo tissue has not been established. We describe methods to culture human large airway explants, small airway explants, and precision-cut lung slices for at least 14 days. Human airway explants recapitulate genotype-specific electrophysiology, characteristic epithelial, endothelial, stromal and immune cell populations, and model viral infection after 14 days in culture. These methods also maintain mouse, rabbit, and pig tracheal explants. Notably, intact airway tissue can be cryopreserved, thawed, and used to generate explants with recovery of function 14 days post-thaw. These studies highlight the broad applications of airway tissue explants and their use as translational intermediates between in vitro and in vivo studies.
    Keywords covid19
    Language English
    Publishing date 2024-02-05
    Publisher Cold Spring Harbor Laboratory
    Document type Article ; Online
    DOI 10.1101/2024.02.03.578756
    Database COVID19

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