scholarly journals Reorganization of multivesicular bodies regulates MHC class II antigen presentation by dendritic cells

2001 ◽  
Vol 155 (1) ◽  
pp. 53-64 ◽  
Author(s):  
Monique Kleijmeer ◽  
Georg Ramm ◽  
Danita Schuurhuis ◽  
Janice Griffith ◽  
Maria Rescigno ◽  
...  

Immature dendritic cells (DCs) sample their environment for antigens and after stimulation present peptide associated with major histocompatibility complex class II (MHC II) to naive T cells. We have studied the intracellular trafficking of MHC II in cultured DCs. In immature cells, the majority of MHC II was stored intracellularly at the internal vesicles of multivesicular bodies (MVBs). In contrast, DM, an accessory molecule required for peptide loading, was located predominantly at the limiting membrane of MVBs. After stimulation, the internal vesicles carrying MHC II were transferred to the limiting membrane of the MVB, bringing MHC II and DM to the same membrane domain. Concomitantly, the MVBs transformed into long tubular organelles that extended into the periphery of the cells. Vesicles that were formed at the tips of these tubules nonselectively incorporated MHC II and DM and presumably mediated transport to the plasma membrane. We propose that in maturing DCs, the reorganization of MVBs is fundamental for the timing of MHC II antigen loading and transport to the plasma membrane.

2013 ◽  
Vol 15 (2) ◽  
pp. 161-167 ◽  
Author(s):  
Bryan Vander Lugt ◽  
Aly A Khan ◽  
Jason A Hackney ◽  
Smita Agrawal ◽  
Justin Lesch ◽  
...  

2003 ◽  
Vol 64 (8) ◽  
pp. 762-770 ◽  
Author(s):  
Manfred Lehner ◽  
Johannes Stöckl ◽  
Otto Majdic ◽  
Walter Knapp ◽  
Katharina Hüttner ◽  
...  

2017 ◽  
Vol 43 (04) ◽  
pp. 285-293 ◽  
Author(s):  
Shih-Chieh Chang ◽  
Yeh-Ku Chen ◽  
Yu-Chun Cheng ◽  
Yi-Chen Chen ◽  
Jiunn-Wang Liao

In this study, canine transmissible venereal tumors (CTVTs) were evaluated for tumor-infiltrating lymphocytes, MHC class II antigen expression, melanoma antigen A (MAGE-A protein), and P-glycoprotein (P-gp). Vincristine (VCR)-sensitive CTVTs (VSCTVTs) were evaluated before and after VCR treatment. Immunohistochemical analysis was performed to evaluate the numbers of CD3[Formula: see text] lymphocytes, CD79a[Formula: see text] lymphocytes, and MHC II[Formula: see text] CTVT cells. Expression levels of P-gp, MAGE-A, and MHC class II antigen were evaluated. The numbers of CD3[Formula: see text] lymphocytes, CD79a[Formula: see text] lymphocytes, and MHC II[Formula: see text] CTVT cells were significantly elevated ([Formula: see text]). After VCR treatment, 100% (8/8) of VSCTVTs exhibited significantly higher MAGE-A expression in CTVT cells, compared with 74% (20/27) of VSCTVTs before VCR treatment. Strong expression of P-gp was found in 14.2% (1/7) of VSCTVTs after VCR treatment compared with VSCTVTs before treatment (83.3%, 5/6). These results demonstrated that regression of VSCTVTs following VCR treatment was associated with an obvious increase in the proportion of MHC class II[Formula: see text] CTVT cells and a significant increase in infiltration by T (CD3[Formula: see text] and B (CD79a[Formula: see text] lymphocytes, as well as decreased expression of P-gp and increased expression of MAGE-A in CTVT cells.


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