| Literature DB >> 34073107 |
Natalia Schiefermeier-Mach1, Violetta Moresco1, Stephan Geley2, Lea Heinrich1, Lukas Lechner1, Heidi Oberhauser1, Susanne Perkhofer1.
Abstract
Inhaled Aspergillus fumigatus spores can be internalized by alveolar type II cells. Cell lines stably expressing fluorescently labeled components of endocytic pathway enable investigations of intracellular organization during conidia internalization and measurement of the process kinetics. The goal of this report was to evaluate the methodological appliance of cell lines for studying fungal conidia internalization. We have generated A549 cell lines stably expressing fluorescently labeled actin (LifeAct-mRuby2) and late endosomal protein (LAMP1-NeonGreen) following an evaluation of cell-pathogen interactions in live and fixed cells. Our data show that the LAMP1-NeonGreen cell line can be used to visualize conidia co-localization with LAMP1 in live and fixed cells. However, caution is necessary when using LifeAct-mRuby2-cell lines as it may affect the conidia internalization dynamics.Entities:
Keywords: Aspergillus fumigatus; LAMP1; LifeAct; cell-pathogen interactions; conidia internalization; live-cell imaging; microscopy; stable cell lines
Year: 2021 PMID: 34073107 DOI: 10.3390/ijms22115965
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923