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集落形成单位-粒细胞巨噬细胞Ia样(HLA-DR)抗原的表达与粒细胞和巨噬细胞生成的调控之间的关联。前列腺素E的新作用。

Association between colony forming units-granulocyte macrophage expression of Ia-like (HLA-DR) antigen and control of granulocyte and macrophage production. A new role for prostaglandin E.

作者信息

Pelus L M

出版信息

J Clin Invest. 1982 Sep;70(3):568-78. doi: 10.1172/jci110649.

Abstract

The expression of Ia-like antigens on human colony forming units-granulocyte macrophage (CFU-GM) is related to S-phase of the cell cycle, and associated with the control of normal granulocyte and macrophage production by prostaglandin E and acidic isoferritins in vitro. Ia-antigen expression by CFU-GM is lost within 3-6 h of culture at 37 degrees C and occurs simultaneously with loss of responsiveness to inhibition by these factors. Culture of bone marrow CFU-GM in a limited exposure suspension culture with 1 microM-1pM prostaglandin E (PGE1 or PGE2), but not prostaglandin F2 alpha or dibutyryl-cyclic-3'-5'-AMP results in the detection of CFU-GM Ia-antigen after 24 h. Antigen expression is associated with an absolute increase in total and S-phase CFU-GM, and restoration of responsiveness to inhibition by prostaglandin E and acidic isoferritins. The detection of Ia-antigen on CFU-GM after suspension culture with prostaglandin E results both from Ia-antigen reexpression as well as stimulation of noncycling cells to enter S-phase, express Ia-antigen and give rise to CFU-GM sensitive to inhibition by prostaglandin E and acidic isoferritins. The sensitivity of CFU-GM to inhibition by these factors after suspension culture with prostaglandin E is identical to that of the same cells tested prior to the suspension culture. These studies provide evidence for a direct regulatory association between Ia-antigen expression and control of myeloid progenitor cell differentiation, and suggest a role for prostaglandin E in the control of CFU-GM cell cycle, Ia-antigen expression, and growth regulation.

摘要

人类集落形成单位-粒细胞巨噬细胞(CFU-GM)上Ia样抗原的表达与细胞周期的S期相关,并与体外前列腺素E和酸性异铁蛋白对正常粒细胞和巨噬细胞生成的控制有关。CFU-GM的Ia抗原表达在37℃培养3-6小时内丧失,且与对这些因子抑制反应性的丧失同时发生。用1微摩尔/升-1皮摩尔/升前列腺素E(PGE1或PGE2),而非前列腺素F2α或二丁酰环磷腺苷在有限暴露悬浮培养中培养骨髓CFU-GM,24小时后可检测到CFU-GM Ia抗原。抗原表达与总CFU-GM和S期CFU-GM的绝对增加以及对前列腺素E和酸性异铁蛋白抑制反应性的恢复有关。用前列腺素E悬浮培养后CFU-GM上Ia抗原的检测既源于Ia抗原的重新表达,也源于非循环细胞被刺激进入S期、表达Ia抗原并产生对前列腺素E和酸性异铁蛋白抑制敏感的CFU-GM。用前列腺素E悬浮培养后CFU-GM对这些因子抑制的敏感性与悬浮培养前测试的相同细胞的敏感性相同。这些研究为Ia抗原表达与髓系祖细胞分化控制之间的直接调节关联提供了证据,并提示前列腺素E在CFU-GM细胞周期控制、Ia抗原表达和生长调节中起作用。

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