Spitzer J A, Zhang P
Department of Physiology, Louisiana State University Medical Center, New Orleans 70112-1393, USA.
Inflammation. 1996 Oct;20(5):485-98. doi: 10.1007/BF01487041.
Several lines of evidence indicate sexual dimorphism in the immune response. We explored gender differences in phagocytosis by neutrophils (PMNs), CD11b/c expression, generation of cytokine-induced neutrophil chemoattractant (CINC) and the influence of developmental stages on some of these parameters. Phagocytosis by PMNs of reproductive female rats was not suppressed by anesthesia and surgery as it was in age-matched males. The phagocytic response to an endotoxir (ET) challenge was also higher in PMNs of reproductive females than in males or in prereproductive or postreproductive females. CINC generation in reproductive females was lower than in age-matched males. Phagocytosis in saline-treated postreproductive females was reduced compared to reproductive and prereproductive females, but was not different from adult males. CD11b/c expression was greater in PMNs of saline treated postreproductive females, than in reproductive or prereproductive animals, but an ET challenge upregulated CD11b/c expression to the same level in all three groups. No gender difference was observed in this parameter. These data indicate that in terms of phagocytosis PMNs of reproductive female rats are more resistant to the effects of anesthesia and surgery and respond to an ET challenge more vigorously than cells of age-matched males. CINC generation in adult rats is also gender dependent. The developmental stages in females modulate phagocytosis and beta 2-integrin expression in PMNs.
多项证据表明免疫反应存在性别差异。我们探究了中性粒细胞(PMN)吞噬作用、CD11b/c表达、细胞因子诱导的中性粒细胞趋化因子(CINC)生成方面的性别差异,以及发育阶段对其中一些参数的影响。与年龄匹配的雄性大鼠不同,麻醉和手术并未抑制成年雌性大鼠PMN的吞噬作用。生殖期雌性大鼠PMN对内毒素(ET)刺激的吞噬反应也高于雄性大鼠或生殖前期或生殖后期的雌性大鼠。生殖期雌性大鼠的CINC生成低于年龄匹配的雄性大鼠。与生殖期和生殖前期雌性大鼠相比,生理盐水处理的生殖后期雌性大鼠的吞噬作用降低,但与成年雄性大鼠无差异。生理盐水处理的生殖后期雌性大鼠PMN的CD11b/c表达高于生殖期或生殖前期动物,但ET刺激使三组的CD11b/c表达上调至相同水平。在该参数上未观察到性别差异。这些数据表明,在吞噬作用方面,成年雌性大鼠的PMN对麻醉和手术的影响更具抵抗力,并且比年龄匹配的雄性大鼠的细胞对ET刺激反应更强烈。成年大鼠的CINC生成也存在性别依赖性。雌性大鼠的发育阶段调节PMN的吞噬作用和β2整合素表达。