Two pathways exist within vertebrate cells to generate peptides for re
cognition by T cells, The ''endogenous'' pathway provides peptides to
MHC class I molecules for presentation to CD8(+) T cells, These peptid
es are derived from proteins synthesized or residing in the cytoplasm
or nucleus, and involves proteasomes and the ubiquitin pathway of prot
ein degradation, as well as a specific peptide transporter (TAP) that
allows these peptides access to the lumen of the endoplasmic reticulum
. The exogenous pathway provides peptides to MHC class II molecules fo
r presentation to CD4(+) T cells. These peptides are derived from extr
acellular antigens taken up by endocytosis and degraded in the endosom
al/lysosomal pathway. Peptide loading of MHC class If molecules requir
es the presence of a molecule (H-2M in mouse, HLA-DM in humans) that i
s structurally related to MHC class II molecules, but the mechanistic
basis of this requirement is unknown, The class II region of the MHC c
ontains a cluster of genes encoding proteins involved in antigen proce
ssing, including genes for two proteasome subunits (LMP2 and LMP7), th
e peptide transporter heterodimer (TAP1 and TAP2), and the H-SM/HLA-DM
molecule (Ma and Mb, or DMA and DMB).