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Departments of 1 Kinesiology and 2 Pharmaceutical Sciences, Washington State University, Pullman, Washington 99164-1410
Received 8 January 1997; accepted in final form 6 May 1997.
Blank, Sally E., T. Bucky Jones, Eric G. Lee, C. Jayne
Brahler, Randle M. Gallucci, Marne L. Fox, and Gary G. Meadows. Modulation of NK cell cytolytic activity by macrophages in chronically exercise-stressed mice. J. Appl.
Physiol. 83(3): 845-850, 1997.
This study was
designed to investigate the effects of moderate-intensity endurance
training on basal natural killer (NK) cell cytolytic activity in murine
splenocytes that were enriched for
1)
NK1.1+ cells or
2) macrophages and
NK1.1+ cells. Mice were assigned
to sedentary (Sed), treadmill control (TM), or treadmill-trained (Trn)
groups. Splenocyte number, the percentages of
NK1.1+, large granular lymphocytes
(NK1.1+, LGL-1+),
and other subpopulations did not change in Trn mice. Approximately 70%
of cells enriched for NK1.1+
expressed this surface antigen. Lytic units (LU) expressed per LGL-1+ cell were significantly
lower in Trn [83.9 ± 3.2 (SE)] compared with Sed (109.5 ± 7.5) and TM (101.3 ± 6.4) groups. When macrophages remained
in the in vitro assay, LU per
LGL-1+ cell did not differ across
groups. The results indicate that highly enriched
NK1.1+ cells from Trn mice had
lower NK cell activity compared with Sed mice. No differences in NK
cell activity were observed when cells were enriched for
NK1.1+ cells and macrophages.
These findings support the hypothesis that macrophage modulation of NK
cells may be one mechanism contributing to augmented basal NK cell
activity in endurance-trained individuals.
endurance training; juxtacrine and paracrine regulation
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