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Properties and requirements for production of a macrophage product which suppresses steroid production by adrenocortical cells.

机译:抑制肾上腺皮质细胞类固醇产生的巨噬细胞产物的性质和要求。

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摘要

Lipopolysaccharide-treated murine peritoneal exudate macrophages (PEM) release a factor or factors into the supernatant that suppress adrenocorticotropic hormone-induced steroidogenesis in explanted rabbit adrenocortical cells (J. C. Mathison et al., J. Immunol. 130:2757-2762, 1983). To determine the requirements for suppression, PEM supernatants (30 microliters) were added to explanted rabbit adrenocortical cells in a final volume of 120 microliters with 10 mU of adrenocorticotropic hormone per ml, and after 18 h at 37 degrees C, steroid concentrations were measured by a fluorometric assay. Supernatant from proteose peptone-elicited C3HeB/FeJ PEM (5 X 10(6) PEM per 3.5-cm well, 10 micrograms of Salmonella minnesota Re595 LPS per ml, 18 h) suppressed steroid production ca. 50%, and kinetic studies demonstrated that the appearance of suppressive activity in the supernatant was gradual over 4 to 18 h. Release of suppressive activity was not associated with decreased viability of the PEM (assessed by fluorescein diacetate staining and measurement of lactic dehydrogenase in the supernatant). Suppression was not observed when the PEM supernatant was diluted 10-fold before addition to the adrenocortical cells, whereas supernatant concentrated 20-fold (prepared with a 10,000-molecular-weight-cutoff filter) produced 75 to 80% suppression. The suppressive activity was stable at pH 4, pH 11, or 70 degrees C for 30 min but was inactivated at 100 degrees C (10 min). Suppressive activity was also induced in C3HeB/FeJ PEM by O111:B4 lipopolysaccharide or heat-killed Listeria monocytogenes. In contrast, PEM from C3H/HeJ mice did not produce detectable suppressive activity in response to Re595 lipopolysaccharide or heat-killed L. monocytogenes. Thus, these results provide additional support for the inducible, selective release of a macrophage product that could affect the host response to lipopolysaccharide by regulation of the adrenocortical response to adrenocorticotropic hormone.
机译:脂多糖处理的小鼠腹膜分泌液巨噬细胞(PEM)在上清液中释放一种或多种因子,抑制上皮性促肾上腺皮质激素诱导的兔肾上腺皮质细胞中类固醇生成(J. C. Mathison等,J。Immunol。130:2757-2762,1983)。为了确定抑制的要求,将PEM上清液(30微升)以120微升的最终体积添加到已移植的兔肾上腺皮质细胞中,每毫升含10 mU促肾上腺皮质激素,并在37摄氏度下18小时后,通过荧光测定。蛋白质p诱导的C3HeB / FeJ PEM(每3.5厘米孔5 X 10(6)PEM,每毫升10毫克明尼苏达沙门氏菌Re595 LPS,18 h)上清液抑制类固醇的产生。 50%的动力学研究表明,在4至18小时内,上清液中抑制活性的出现是逐渐的。抑制活性的释放与PEM活力的降低无关(通过荧光素双乙酸酯染色和上清液中乳酸脱氢酶的测定进行评估)。在将PEM上清液稀释至添加至肾上腺皮质细胞之前稀释10倍时未观察到抑制,而浓缩20倍的上清液(用10,000分子量截止滤膜制备)则产生了75%至80%的抑制作用。抑制活性在pH 4,pH 11或70摄氏度下稳定30分钟,但在100摄氏度下失活(10分钟)。还通过O111:B4脂多糖或热杀死的单核细胞增生李斯特菌在C3HeB / FeJ PEM中诱导了抑制活性。相比之下,来自C3H / HeJ小鼠的PEM对Re595脂多糖或热灭活的单核细胞增生李斯特菌没有产生可检测的抑制活性。因此,这些结果为巨噬细胞产物的诱导性,选择性释放提供了额外的支持,该产物可能通过调节对促肾上腺皮质激素的肾上腺皮质反应来影响宿主对脂多糖的应答。

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