Direct vesicular transport of MHC class II molecules from lysosomal structures to the cell surface.

Author:

Wubbolts R1,Fernandez-Borja M1,Oomen L1,Verwoerd D1,Janssen H1,Calafat J1,Tulp A1,Dusseljee S1,Neefjes J1

Affiliation:

1. Department of Cellular Biochemistry, The Netherlands Cancer Institute, Amsterdam, The Netherlands.

Abstract

Newly synthesized MHC class II molecules are sorted to lysosomal structures where peptide loading can occur. Beyond this point in biosynthesis, no MHC class II molecules have been detected at locations other than the cell surface. We studied this step in intracellular transport by visualizing MHC class II molecules in living cells. For this purpose we stably expressed a modified HLA-DR1 beta chain with the Green Fluorescent Protein (GFP) coupled to its cytoplasmic tail (beta-GFP) in class II-expressing Mel JuSo cells. This modification of the class II beta chain does not affect assembly, intracellular distribution, and peptide loading of the MHC class II complex. Transport of the class II/ beta-GFP chimera was studied in living cells at 37 degrees C. We visualize rapid movement of acidic class II/beta-GFP containing vesicles from lysosomal compartments to the plasma membrane and show that fusion of these vesicles with the plasma membrane occurs. Furthermore, we show that this transport route does not intersect the earlier endosomal pathway.

Publisher

Rockefeller University Press

Subject

Cell Biology

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