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新鲜和储存粒细胞中的刺激-反应偶联

Stimulus-response coupling in fresh and stored granulocytes.

作者信息

Lane T A, Lamkin G E

机构信息

Laboratory Service, Veterans Administration Medical Center, San Diego, California.

出版信息

Transfusion. 1988 May-Jun;28(3):243-7. doi: 10.1046/j.1537-2995.1988.28388219152.x.

Abstract

Granulocytes stored in the blood bank prior to transfusion undergo progressive decrements in their ability to circulate and migrate in vivo and to migrate in vitro (chemotaxis). The pathogenesis of granulocyte (PMN) chemotaxis (CTX) dysfunction after room-temperature storage of PMN is unclear. Previous work in the authors' laboratory and others led to the hypothesis that intracellular transmission of chemotactic signals, referred to as stimulus-response coupling (SRC), might be abnormal in stored PMN. This report presents an investigation of the ability of fresh and stored PMN to generate and respond to leukotriene-B4 (LTB4), the chief intracellular amplifier of SRC for CTX. PMN were sampled from concentrates within 4 hours of collection and after 24 and 48 hours of storage in transfer packs at room temperature (RT). Fresh, stimulated PMN synthesized 202 +/- 51 ng of LTB4 and 110 +/- 11 ng of 5-hydroxyeicosatetraenoic acid (HETE) per 10(7) PMN. Synthesis of LTB4, but not HETE was significantly decreased after 24 hours' storage, and LTB4 and HETE synthesis decreased after 48 hours. The incubation of stored PMN with arachidonic acid (AA) maintained levels of LTB4 synthesis in PMN stored for 24 but not 48 hours. Also, the CTX defect of stored PMN to F-Met-Leu-Phe (FMLP) was not improved by the supplementation of PMN with exogenous sources of LTB4 or AA.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

输血前储存在血库中的粒细胞在体内循环和迁移以及体外迁移(趋化作用)的能力会逐渐下降。中性粒细胞(PMN)在室温储存后趋化作用(CTX)功能障碍的发病机制尚不清楚。作者实验室及其他机构之前的研究提出了一个假设,即趋化信号的细胞内传递,即刺激-反应偶联(SRC),在储存的PMN中可能异常。本报告介绍了对新鲜和储存的PMN产生和对白三烯-B4(LTB4)反应能力的研究,LTB4是CTX的SRC主要细胞内增强剂。在采集后4小时内以及在室温(RT)下于转移包中储存24小时和48小时后,从浓缩物中采集PMN。新鲜的、受刺激的PMN每10⁷个PMN合成202±51 ng的LTB4和110±11 ng的5-羟基二十碳四烯酸(HETE)。储存24小时后LTB4的合成显著下降,但HETE的合成未下降,48小时后LTB4和HETE的合成均下降。用花生四烯酸(AA)孵育储存的PMN可维持储存24小时而非48小时的PMN中LTB4的合成水平。此外,用外源性LTB4或AA补充PMN并不能改善储存的PMN对F-甲硫氨酰-亮氨酰-苯丙氨酸(FMLP)的CTX缺陷。(摘要截短于250字)

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