Shephard Roy J
Faculty of Physical Education and Health, and Department of Public Health Sciences, University of Toronto, Toronto, Ontario, Canada.
Sports Med. 2003;33(4):261-84. doi: 10.2165/00007256-200333040-00002.
The circulating blood normally contains no more than 1-2% of the body's population of leucocytes. The numbers and phenotypes of circulating leucocyte subsets can change dramatically during and immediately following exercise. The surface expression of adhesion molecules makes an important contribution to such responses by changing patterns of cell trafficking. Alterations in the surface expression of adhesion molecules could reflect a shedding of molecules, selective apoptosis or differential trafficking of cells with a particular phenotype, effects from mechanical deformation of the cytoplasm, active biochemical processes involving cytokines, catecholamines, glucocorticoids or other hormones, or changes in the induction of adhesion molecules. The expression of adhesion molecules changes with maturation and activation of leucocytes. Typically, mature cells express lower densities of L-selectin (CD62L), the homing receptor for secondary lymphoid organs, and higher densities of LFA-1 (CD11a), the molecule associated with trafficking to non-lymphoid reservoir sites. The neutrophils and natural killer cells that are mobilised during exercise also express high levels of Mac-1 (CD11b), a marker associated with cellular activation. Possibly, exercise demarginates older cells that are awaiting destruction in the spleen. Plasma concentrations of catecholamines rise dramatically with exercise, and there is growing evidence that catecholamines, acting through a cyclic adenosine monophosphate second messenger system, play an important role in modifying the surface expression of adhesion molecules. Analogous changes can be induced by other forms of stress that release catecholamines or by catecholamine infusion, and responses are blocked by beta(2)-blocking agents. Catecholamines also modify adherence and expression of adhesion molecules in vitro. Cell trafficking is modified by genetic deficiencies in the expression of adhesion molecules, but leucocyte responses to exercise and catecholamines are generally unaffected by splenectomy. A number of clinical conditions including atherogenesis and metaplasia are marked by an altered expression of adhesion molecules. The effects of exercise on these molecules could thus have important health implications.
正常情况下,循环血液中所含白细胞数量不超过人体白细胞总数的1%-2%。运动期间及运动刚结束后,循环白细胞亚群的数量和表型会发生显著变化。黏附分子的表面表达通过改变细胞运输模式,对这些反应起到重要作用。黏附分子表面表达的改变可能反映出分子脱落、选择性凋亡或特定表型细胞的差异性运输、细胞质机械变形的影响、涉及细胞因子、儿茶酚胺、糖皮质激素或其他激素的活跃生化过程,或者黏附分子诱导的变化。黏附分子的表达会随着白细胞的成熟和激活而改变。通常,成熟细胞表达较低密度的L-选择素(CD62L),即二级淋巴器官的归巢受体,以及较高密度的淋巴细胞功能相关抗原-1(LFA-1,CD11a),该分子与向非淋巴储存部位的运输有关。运动期间动员的中性粒细胞和自然杀伤细胞也表达高水平的巨噬细胞-1(Mac-1,CD11b),这是一种与细胞激活相关的标志物。运动可能会使原本在脾脏中等待被清除的衰老细胞进入循环。运动时血浆儿茶酚胺浓度会急剧上升,越来越多的证据表明,儿茶酚胺通过环磷酸腺苷第二信使系统发挥作用,在调节黏附分子的表面表达方面起着重要作用。其他释放儿茶酚胺的应激形式或儿茶酚胺输注也能诱导类似变化,且这些反应可被β₂受体阻滞剂阻断。儿茶酚胺在体外也会改变黏附分子的黏附及表达。黏附分子表达的基因缺陷会改变细胞运输,但白细胞对运动和儿茶酚胺的反应通常不受脾切除的影响。包括动脉粥样硬化和化生在内的一些临床病症,其特征是黏附分子表达改变。因此,运动对这些分子的影响可能具有重要的健康意义。