Kurokawa Y, Shinkai S, Torii J, Hino S, Shek P N
Department of Hygiene and Public Health, Ehime University School of Medicine, Japan.
Eur J Appl Physiol Occup Physiol. 1995;71(2-3):245-52. doi: 10.1007/BF00854986.
This study examined the relationship between exercise-induced changes in the concentration of circulating immunocompetent cells and their surface expression of adhesion molecules: L-selectin (CD62L) and three beta 2-integrins [LFA-1(CD11a/CD18), Mac-1 (CD11b/CD18), and p150/95(CD11c/CD18)]. Eight young male volunteers exercised on a cycle ergometer for 60 min at 60% maximal oxygen uptake. Peripheral blood samples, collected every 30 min throughout exercise and during the 2-h recovery period, were used for flow-cytometric analysis. The experimental results were compared with control data obtained ever 60 min at corresponding times of the nonexercise day. The exercise regimen induced a granulocytosis and a lymphocytosis, mainly due to an elevation of CD8+ and CD16+ cells. During recovery, a further granulocytosis occurred but accompanied by a lymphopenia. The increased CD8+ cell-count during exercise was characterized by a selective mobilization of the CD62L- and CD11ahigh cells, i.e. primed CD8+ cells. A postexercise suppression of CD4+ cell-count was derived only from CD62L+ cells. The CD11b+ and CD11c+ lymphocytes also increased during exercise, largely attributable to an increase in CD16+ cells which co-expressed CD11b and CD11c molecules. The CD62L surface density of granulocytes increased significantly during recovery. This resulted from a selective influx of CD62Lhigh granulocytes into the circulation. There were no significant changes in per-cell density of the three beta 2-integrins on granulocytes and lymphocytes throughout the experimental period. These results suggest that the cell-surface expression of CD62L (and CD11a) molecules is associated with the differential mobilization of CD8+ cells during exercise, the postexercise suppression of CD4+ cell-counts and the granulocytosis following exercise.
L-选择素(CD62L)和三种β2整合素[淋巴细胞功能相关抗原-1(LFA-1,CD11a/CD18)、巨噬细胞-1(Mac-1,CD11b/CD18)和p150/95(CD11c/CD18)]。八名年轻男性志愿者在自行车测力计上以最大摄氧量的60%进行了60分钟的运动。在运动过程中每30分钟以及在2小时恢复期间采集外周血样本,用于流式细胞术分析。将实验结果与在非运动日相应时间每隔60分钟获得的对照数据进行比较。运动方案诱导了粒细胞增多和淋巴细胞增多,主要是由于CD8+和CD16+细胞数量增加。在恢复过程中,进一步出现了粒细胞增多,但伴有淋巴细胞减少。运动期间CD8+细胞计数增加的特征是CD62L和CD11a高表达细胞(即致敏CD8+细胞)的选择性动员。运动后CD4+细胞计数的抑制仅源于CD62L+细胞。运动期间CD11b+和CD11c+淋巴细胞也增加,这在很大程度上归因于共表达CD11b和CD11c分子的CD16+细胞数量增加。恢复期间粒细胞的CD62L表面密度显著增加。这是由于CD62L高表达粒细胞选择性流入循环所致。在整个实验期间,粒细胞和淋巴细胞上三种β2整合素的每细胞密度没有显著变化。这些结果表明,CD62L(和CD11a)分子的细胞表面表达与运动期间CD8+细胞的差异动员、运动后CD4+细胞计数的抑制以及运动后的粒细胞增多有关。