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Natural glucocorticoids induce expansion of all developmental stages of murine bone marrow granulocytes without inhibiting function

淋巴细胞生成 粒细胞 髓样 骨髓 骨髓生成 吞噬作用 造血 免疫学 生物 淋巴细胞 趋化性 流式细胞术 皮质酮 髓过氧化物酶 祖细胞 化学 男科 内分泌学 细胞生物学 炎症 生物化学 干细胞 医学 受体 激素
作者
Mark Trottier,Matthew M. Newsted,Louis E. King,Pamela J. Fraker
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:105 (6): 2028-2033 被引量:85
标识
DOI:10.1073/pnas.0712003105
摘要

Natural glucocorticoids (Gc) produced during stress have profound effects on the immune system. It is well known that Gc induce apoptosis in precursor T and B cells, markedly altering lymphopoiesis. However, it has been noted that marrow myeloid cells expanded both in proportion and absolute numbers in the mouse after Gc exposure. Mice were implanted with a corticosterone (CS) tablet that increased serum Gc and caused atrophied thymuses, both classic signs of activation of the stress axis. Blood neutrophil counts were elevated (4.8x), whereas lymphocyte counts declined. Flow cytometric analysis of the marrow revealed that the phenotypic distribution of the various major classes of cells was shifted by Gc exposure. As expected, marrow lymphocyte numbers declined >40% after 3 days of exposure to Gc. Conversely, in the myeloid compartment, both monocytes and granulocytes increased in number by >40%. Further, all granulocyte developmental stages showed large increases in both total number and percentage of cells. To investigate the functional capacity of mature granulocytes from Gc-treated mice, an improved granulocyte isolation method was developed. Gc exposure had little effect on the ability of granulocytes to produce superoxide or undergo chemotaxis or phagocytose bacteria. These results indicate that Gc treatment shifts bone marrow composition and provides evidence that granulocytes and their progenitors are selectively preserved under stressful conditions without losing function.
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