Structural study of lipid droplet using synchrotron label-free multimodal imaging

Autor: Jamme, Frederic, Bouchez, Isabelle, Pénicaud, Caroline, Passot, Stéphanie, Fonseca, Fernanda, Gohon, Yann, Réfrégiers, Mathieu, Pereiro, Eva, Cinquin, Bertrand, Froissard, Marine
Přispěvatelé: Synchrotron SOLEIL, Institut Jean-Pierre Bourgin (IJPB), Institut National de la Recherche Agronomique (INRA)-AgroParisTech, Université Paris Saclay (COmUE), Génie et Microbiologie des Procédés Alimentaires (GMPA), ALBA Synchrotron light source [Barcelone], Laboratoire de Biologie et de Pharmacologie Appliquée (LBPA), École normale supérieure - Cachan (ENS Cachan)-Centre National de la Recherche Scientifique (CNRS), Centre National de la Recherche Scientifique (CNRS). FRA.
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Zdroj: 4th International Conference on Physics and Biological Systems 2018. 2018; 4. International Conference on Physics and Biological Systems, Gif-sur-Yvette, FRA, 2018-10-22-2018-10-24, 1 p.
4. International Conference on Physics and Biological Systems
4. International Conference on Physics and Biological Systems, Oct 2018, Gif-sur-Yvette, France. 2018, 4th International Conference on Physics and Biological Systems 2018
Popis: National audience; Imaging intracellular compartments, their dynamics and interactions in living cells, remains challenging. Using various lipid droplet (LD) protein markers, we revealed inter LD heterogeneity at single cell level, due to LD specific geolocalisation and enzymatic equipment. Even so, using tagged proteins or vital probes could modify the morphology and the smooth running of the organelles. Methods based on intrinsic fluorescence of molecules upon excitation by deep ultra violet (DUV) illumination are thus emerging for living cell imaging. We used DUV from synchrotron radiation to perform autofluorescence and transmittance imaging on single living yeast. The contrasted signals inside the cells revealed chemical heterogeneity at the subcellular level. Microscopy showed organelles with low auto-fluorescence after DUV illumination. We distinguished two populations, with high or low transmittance. The first population corresponded to vacuoles and the second to LDs. LDs appeared as heterogeneous well-organized structures with a low transmittance zone on the surface and a high transmittance core. We propose that the low transmittance ring and the high transmittance core correspond to ergosterol and triacylglycerol-containing structures, respectively. The conclusions we drawn using DUV imaging were confirmed by experiments performed using soft X ray imaging on cryofixed cells. Synchrotron label free imaging paves the way for efficient structural and dynamic studies of LDs and other organelles.
Databáze: OpenAIRE