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载体上清液对砷化镓诱导的抗体形成细胞反应抑制的逆转作用。I. 体外和体内暴露后的药代动力学

Reversal of gallium arsenide-induced suppression of the antibody-forming cell response by vehicle supernatants. I. Pharmacokinetics after in vitro and in vivo exposure.

作者信息

Burns L A, Munson A E

机构信息

Department of Pharmacology and Toxicology, Medical College of Virginia, Virginia Commonwealth University, Richmond.

出版信息

J Pharmacol Exp Ther. 1993 Apr;265(1):144-9.

PMID:8386233
Abstract

Exposure of splenocytes in vivo or in vitro to gallium arsenide (GaAs) dose-dependently suppresses the ability of these cells to produce antibody after in vitro immunization with sheep red blood cells. In addition, it has been demonstrated that GaAs exerts immunosuppressive effects early (36 hr) in the generation of a primary antibody-forming cell (AFC) response. The objective of this study was to determine if the GaAs-induced suppression was produced as a result of a GaAs-induced alteration in the secretion of soluble mediators. Supernatants from in vivo and in vitro vehicle (VH)-exposed splenocyte cultures time-dependently reversed GaAs-induced suppression of the in vitro-generated primary AFC response produced by both in vitro (50 microM) and in vivo (200 mg/kg) exposure to GaAs. Supernatants from in vitro GaAs-exposed cells suppressed the VH response 40, 89 and 93% at 24, 36 and 48 hr, respectively. Using the arsenic-binding compound meso-2,3-dimercaptosuccinic acid (100 microM), it was determined that the suppression of the VH response by supernatants from in vitro GaAs-exposed cultures was confounded by the presence of free arsenic in the in vitro GaAs-exposed culture supernatant. In contrast, suppression of in vivo VH-exposed AFC responses by supernatants from in vivo GaAs-exposed cells was not seen. The time-dependent reversal of immunosuppression produced by in vivo or in vitro exposure to GaAs, by supernatants from in vivo and in vitro VH-exposed cells mimics the reported kinetics of suppression by addition of GaAs to antibody cultures.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

体内或体外将脾细胞暴露于砷化镓(GaAs),会剂量依赖性地抑制这些细胞在体外用绵羊红细胞免疫后产生抗体的能力。此外,已证明GaAs在初次抗体形成细胞(AFC)反应产生的早期(36小时)发挥免疫抑制作用。本研究的目的是确定GaAs诱导的抑制作用是否是由于GaAs诱导的可溶性介质分泌改变所致。体内和体外暴露于赋形剂(VH)的脾细胞培养物的上清液可随时间依赖性地逆转GaAs诱导的体外产生的初次AFC反应的抑制作用,该抑制作用由体外(50 microM)和体内(200 mg/kg)暴露于GaAs引起。体外暴露于GaAs的细胞的上清液在24、36和48小时分别抑制VH反应40%、89%和93%。使用砷结合化合物内消旋-2,3-二巯基琥珀酸(100 microM),确定体外暴露于GaAs的培养物的上清液对VH反应的抑制作用因体外暴露于GaAs的培养上清液中存在游离砷而受到混淆。相比之下,未观察到体内暴露于GaAs的细胞的上清液对体内暴露于VH的AFC反应的抑制作用。体内或体外暴露于GaAs所产生的免疫抑制作用随时间的逆转,由体内和体外暴露于VH的细胞的上清液模拟了向抗体培养物中添加GaAs所报告的抑制动力学。(摘要截短于250字)

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