Details

Autor(en) / Beteiligte

• Di Martino, Julie
• Mascalchi, Patrice
• Legros, Philippe
• Lacomme, Sabrina
• Gontier, Etienne
• Bioulac‐Sage, Paulette
• Balabaud, Charles
• Moreau, Violaine
• Saltel, Frédéric

Titel

STED microscopy: A simplified method for liver sinusoidal endothelial fenestrae analysis

Ist Teil von

• Biology of the cell, 2018-07, Vol.110 (7), p.159-168

Ort / Verlag

England

Erscheinungsjahr

2018

Quelle

MEDLINE

Beschreibungen/Notizen

• Background Information Liver sinusoidal endothelial cells (LSECs) possess fenestrae, open transcellular pores with an average diameter of 100 nm. These fenestrae allow for the exchange between blood and hepatocytes. Alterations in their number or diameter in liver diseases have important implications for hepatic microcirculation and function. Although decades of studies, fenestrae are still observed into fixed cells and we have poor knowledge of their dynamics. Results Using stimulated emission depletion (STED) super‐resolution microscopy, we have established a faster and simplest method to observe and quantify fenestrae. Indeed, using cytochalasin D, an actin depolymerising agent known to promote fenestrae formation, we measure the increase of fenestrae number. We adapted this methodology to develop an automated method to study fenestrae dynamics. Moreover, with two‐colour STED analysis, we have shown that this approach could be useful to study LSECs fenestrae molecular composition. Conclusions Our approach demonstrates that STED microscopy is suitable for LSEC fenestrae study. Significance This new way of analysing LSEC fenestrae will allow for expedited investigation of their dynamics, molecular composition and functions to better understand their function in liver pathophysiology. Research article This study highlights that stimulated‐emission‐depletion (STED) microscopy is perfectly adapted for visualization, quantification, dynamics and molecular analysis of Liver sinusoidal endothelial cells (LSECs) fenestrae. Indeed, after fluorescence staining of the cell membrane or cytoplasm and using this super resolution optical microscopy method, we created a simple strategy for LSECs fenestrae analysis.