scholarly journals Plasma Membrane Lipid Domains as Platforms for Vesicle Biogenesis and Shedding?

Biomolecules ◽  
2018 ◽  
Vol 8 (3) ◽  
pp. 94 ◽  
Author(s):  
Hélène Pollet ◽  
Louise Conrard ◽  
Anne-Sophie Cloos ◽  
Donatienne Tyteca

Extracellular vesicles (EVs) contribute to several pathophysiological processes and appear as emerging targets for disease diagnosis and therapy. However, successful translation from bench to bedside requires deeper understanding of EVs, in particular their diversity, composition, biogenesis and shedding mechanisms. In this review, we focus on plasma membrane-derived microvesicles (MVs), far less appreciated than exosomes. We integrate documented mechanisms involved in MV biogenesis and shedding, focusing on the red blood cell as a model. We then provide a perspective for the relevance of plasma membrane lipid composition and biophysical properties in microvesiculation on red blood cells but also platelets, immune and nervous cells as well as tumor cells. Although only a few data are available in this respect, most of them appear to converge to the idea that modulation of plasma membrane lipid content, transversal asymmetry and lateral heterogeneity in lipid domains may play a significant role in the vesiculation process. We suggest that lipid domains may represent platforms for inclusion/exclusion of membrane lipids and proteins into MVs and that MVs could originate from distinct domains during physiological processes and disease evolution.

2021 ◽  
Vol 120 (3) ◽  
pp. 46a
Author(s):  
Filipa C. Santos ◽  
Andreia S. Fernandes ◽  
Arnaldo Videira ◽  
Rodrigo F.M. De Almeida

2016 ◽  
Vol 110 (3) ◽  
pp. 638a
Author(s):  
Thorsten Wohland ◽  
Xue Wen Ng ◽  
Cathleen Teh ◽  
Vladimir Korzh

2007 ◽  
Vol 149 ◽  
pp. S17
Author(s):  
Wendy Jessup ◽  
Todd Mitchell ◽  
David Willimson ◽  
Len Kritharides ◽  
Katharina Gaus

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
C. Leonard ◽  
L. Conrard ◽  
M. Guthmann ◽  
H. Pollet ◽  
M. Carquin ◽  
...  

Author(s):  
Filipa C. Santos ◽  
Andreia S. Fernandes ◽  
Catarina A.C. Antunes ◽  
Filipe P. Moreira ◽  
Arnaldo Videira ◽  
...  

2021 ◽  
Vol 7 (7) ◽  
pp. 514
Author(s):  
Mariangela Dionysopoulou ◽  
George Diallinas

Recent biochemical and biophysical evidence have established that membrane lipids, namely phospholipids, sphingolipids and sterols, are critical for the function of eukaryotic plasma membrane transporters. Here, we study the effect of selected membrane lipid biosynthesis mutations and of the ergosterol-related antifungal itraconazole on the subcellular localization, stability and transport kinetics of two well-studied purine transporters, UapA and AzgA, in Aspergillus nidulans. We show that genetic reduction in biosynthesis of ergosterol, sphingolipids or phosphoinositides arrest A. nidulans growth after germling formation, but solely blocks in early steps of ergosterol (Erg11) or sphingolipid (BasA) synthesis have a negative effect on plasma membrane (PM) localization and stability of transporters before growth arrest. Surprisingly, the fraction of UapA or AzgA that reaches the PM in lipid biosynthesis mutants is shown to conserve normal apparent transport kinetics. We further show that turnover of UapA, which is the transporter mostly sensitive to membrane lipid content modification, occurs during its trafficking and by enhanced endocytosis, and is partly dependent on autophagy and Hect-type HulARsp5 ubiquitination. Our results point out that the role of specific membrane lipids on transporter biogenesis and function in vivo is complex, combinatorial and transporter-dependent.


Lipids ◽  
1988 ◽  
Vol 23 (9) ◽  
pp. 829-833 ◽  
Author(s):  
Michael W. Hamm ◽  
Anna Sekowski ◽  
Roni Ephrat

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