Regulation of Adaptive Immunity by Cells of the Innate Immune System: Bone Marrow Natural Killer Cells Inhibit T Cell Proliferation

Author(s):  
Prachi P. Trivedi ◽  
Taba K. Amouzegar ◽  
Paul C. Roberts ◽  
Norbert A. Wolf ◽  
Robert H. Swanborg
2008 ◽  
Vol 83 (5) ◽  
pp. 1128-1135 ◽  
Author(s):  
Taba Kheradmand ◽  
Prachi P. Trivedi ◽  
Norbert A. Wolf ◽  
Paul C. Roberts ◽  
Robert H. Swanborg

2006 ◽  
Vol 7 (5) ◽  
pp. 507-516 ◽  
Author(s):  
Jacqueline G O'Leary ◽  
Mahmoud Goodarzi ◽  
Danielle L Drayton ◽  
Ulrich H von Andrian

1993 ◽  
Vol 75 (6) ◽  
pp. 2734-2739 ◽  
Author(s):  
J. W. Armstrong ◽  
K. A. Nelson ◽  
S. J. Simske ◽  
M. W. Luttges ◽  
J. J. Iandolo ◽  
...  

The effects of skeletal unloading using antiorthostatic tail suspension on the mouse immune system are tissue specific. This phenomenon was demonstrated by analyzing cells from the lymph nodes, spleen, and bone marrow. Phytohemagglutinin-induced T-cell proliferation was depressed in lymph nodes after 11 days of antiorthostatic suspension. In contrast, splenic T-cell proliferation in response to phytohemagglutinin was enhanced. Splenic natural killer cell cytotoxicity was unchanged after suspension, which demonstrated the organ- and cell-specific effects of skeletal unloading. Whereas antiorthostatic suspension induced minimal changes in bone, there was a significant depression in the number of macrophage precursors in the bone marrow. Overall, skeletally unloaded animals had slightly higher blood corticosterone levels than did control animals; however, it did not appear to be responsible for the observed changes. In conclusion, skeletal unloading produces organ- and cell-specific changes in the murine immune system rather than a generalized immunosuppression.


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