TY - JOUR
T1 - Class II MHC molecules and antigen enter the same vesicles during internalization by resting B lymphocytes
AU - Gosselin, Edmund J.
AU - Parker, David C.
N1 - Funding Information:
’ This work was supported by Grant AI 24303 from the National Institutes of Health. During completion of this project salary was provided by a fellowship from “Friends of the Norris Cotton Cancer Center,” the Norris Cotton Cancer Center, Dartmouth-Hitchcock Medical Center, Hanover, NH. * To whom correspondence should be addressed at the Department of Physiology, Dartmouth Medical School, Hanover, NH 03756. 3 Abbreviations used: Ag, antigen; Ab, antibody; Ig, immunoglobulin; BSA, bovine serum albumin; PBS, phosphate-buffered saline; SEM, standard error of the mean.
PY - 1990/9
Y1 - 1990/9
N2 - Efficient presentation of Ag by a B cell to a T cell requires that Ag bind to the Ag receptor (Ig) on the B cell, after which it is internalized into an acid compartment where it is modified and returned to the cell surface in the context of class II MHC molecules. It remains uncertain whether processed Ag binds to class II which has been internalized and recycled with Ag, or to nascent class II inside the cell. To determine if cell surface class II enters the same vesicles as Ag, or is excluded during internalization of Ag which is bound to the B cell receptor, 5- and 16-nm gold particles were labeled with anti-class II and anti-Ig, respectively. Cells were incubated at 37 °C and internalization of these particles was observed using electron microscopy. By 10 min, 60-75% of the B cell sections contained vesicles with gold particles inside them. Between 40 and 64% of these vesicles had both 5- and 16-nm particles. Maximum internalization occurred by 30-60 min, and by 2 hr the number of small and large particles on the B cell surface became constant or increased, respectively. Both kinds of particles moved from electron-lucent to electron-dense vesicles as the incubation time increased, although a portion of the anti-class II particles remained in electron-lucent vesicles. These data clearly show that labeled, cell surface class II is not selectively excluded from Ag-containing vesicles during Ag internalization. Thus, cointernalization of Ag and class II may represent a mechanism by which processed Ag meets class II.
AB - Efficient presentation of Ag by a B cell to a T cell requires that Ag bind to the Ag receptor (Ig) on the B cell, after which it is internalized into an acid compartment where it is modified and returned to the cell surface in the context of class II MHC molecules. It remains uncertain whether processed Ag binds to class II which has been internalized and recycled with Ag, or to nascent class II inside the cell. To determine if cell surface class II enters the same vesicles as Ag, or is excluded during internalization of Ag which is bound to the B cell receptor, 5- and 16-nm gold particles were labeled with anti-class II and anti-Ig, respectively. Cells were incubated at 37 °C and internalization of these particles was observed using electron microscopy. By 10 min, 60-75% of the B cell sections contained vesicles with gold particles inside them. Between 40 and 64% of these vesicles had both 5- and 16-nm particles. Maximum internalization occurred by 30-60 min, and by 2 hr the number of small and large particles on the B cell surface became constant or increased, respectively. Both kinds of particles moved from electron-lucent to electron-dense vesicles as the incubation time increased, although a portion of the anti-class II particles remained in electron-lucent vesicles. These data clearly show that labeled, cell surface class II is not selectively excluded from Ag-containing vesicles during Ag internalization. Thus, cointernalization of Ag and class II may represent a mechanism by which processed Ag meets class II.
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U2 - 10.1016/0008-8749(90)90216-E
DO - 10.1016/0008-8749(90)90216-E
M3 - Article
C2 - 2383898
AN - SCOPUS:0025032333
SN - 0008-8749
VL - 129
SP - 404
EP - 413
JO - Cellular Immunology
JF - Cellular Immunology
IS - 2
ER -