Author/Authors :
Vincent Ng، نويسنده , , George Zanazzi، نويسنده , , Rupert Timpl and Tad A Holak، نويسنده , , Jan F. Talts، نويسنده , , James L Salzer، نويسنده , , Patrick J. Brennan، نويسنده , , Anura Rambukkana، نويسنده ,
Abstract :
The cell wall of pathogenic mycobacteria is abundant with complex glycolipids whose roles in disease pathogenesis are mostly unknown. Here, we provide evidence for the involvement of the specific trisaccharide unit of the phenolic glycolipid-1 (PGL-1) of Mycobacterium leprae in determining the bacterial predilection to the peripheral nerve. PGL-1 binds specifically to the native laminin-2 in the basal lamina of Schwann cell-axon units. This binding is mediated by the α2LG1, α2LG4, and α2LG5 modules present in the naturally cleaved fragments of the peripheral nerve laminin α2 chain, and is inhibited by the synthetic terminal trisaccharide of PGL-1. PGL-1 is involved in the M. leprae invasion of Schwann cells through the basal lamina in a laminin-2-dependent pathway. The results indicate a novel role of a bacterial glycolipid in determining the nerve predilection of a human pathogen.