Modulation of a host's cell membrane nano-environment by mycobacterial glycolipids: involvement of PI(4,5)P 2 signaling lipid?

Virulence-associated glycolipids from ( ) act as effector molecules during infection-in addition to proteins. Upon insertion, they alter the host cell's membrane properties modifying the host's functions to aid survival and disease course. Here we combine tether force experiments and micro...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Faraday discussions 2021-12, Vol.232, p.295-316
Hauptverfasser: Mishra, Manjari, Kapoor, Shobhna
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Virulence-associated glycolipids from ( ) act as effector molecules during infection-in addition to proteins. Upon insertion, they alter the host cell's membrane properties modifying the host's functions to aid survival and disease course. Here we combine tether force experiments and microscopy to reveal previously unknown insights on the potential involvement of the phosphatidylinositol 4,5-bisphosphate (PI(4,5)P ) lipid in the lipid-host interaction landscape. Our data shows that lipids, having different structural and chemical make-up, distinctly alter a host's PI(4,5)P membrane abundance/organization and PI(4,5)P -actin colocalization, thus impacting the plasma membrane-cytoskeletal adhesion forces. Combined with our previous findings that underscore the role of exogenous lipids in remodeling host plasma membrane organization and mechanics, this work builds upon a lipid-centric view of tubercular infections. Dynamically changing a host's plasma membrane lipid content - in response to virulent lipids - might represent a so far unexplored mechanism invoked by to modulate the host cell's adhesive properties to escape immune surveillance. These findings will deepen our collective understanding of the functional role of lipids in hijacking the host cell processes amenable to pharmacological inhibition.
ISSN:1359-6640
1364-5498
DOI:10.1039/d0fd00051e