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多氯联苯混合物1242刺激多形核中性粒细胞中肌醇磷酸的产生。

Aroclor 1242 stimulates the production of inositol phosphates in polymorphonuclear neutrophils.

作者信息

Tithof P K, Contreras M L, Ganey P E

机构信息

Department of Pharmacology and Toxicology, Michigan State University, East Lansing 48824.

出版信息

Toxicol Appl Pharmacol. 1995 Mar;131(1):136-43. doi: 10.1006/taap.1995.1055.

Abstract

Exposure in vitro to the mixture of polychlorinated biphenyls (PCBs), Aroclor 1242, stimulates superoxide anion (O2-) production and degranulation in rat polymorphonuclear neutrophils (PMNs). The mechanism by which PCBs activate PMNs is unknown. Phospholipase C-dependent hydrolysis of membrane phosphoinositides is an important early event in PMN activation in response to several agonists including N-formyl-methionyl-leucyl phenylalanine (fMLP); therefore, the present study was undertaken to determine whether Aroclor 1242 stimulates the production of inositol phosphates in isolated rat PMNs. PMNs elicited with glycogen from rat peritoneum were labeled with myo-[2-3H]inositol, and the effect of fMLP and Aroclor 1242 on accumulation of [3H]inositol phosphates was determined. Both fMLP (in the presence of cytochalasin B) and Aroclor 1242 induced rapid breakdown of inositol-containing phospholipids. Peak accumulation of [3H]inositol phosphates occurred within 5 sec in response to Aroclor 1242 and within 15-30 sec in response to fMLP. In cytochalasin B-treated PMNs, significant O2- generation occurred within 5 min of exposure to fMLP or Aroclor 1242. 2,2',4,4'-Tetrachlorobiphenyl (TCB), but not 3,3',4,4'-TCB, stimulates O2- production and degranulation in isolated rat PMNs. To determine whether inositol phosphate accumulation parallels PMN activation, [3H]inositol monophosphate (IP) production was measured in response to Aroclor 1242, 2,2'4,4'-TCB, and 3,3'4,4'-TCB in LiCl-treated cells. Both Aroclor 1242 and 2,2',4,4'-TCB, but not 3,3',4,4'-TCB, caused significant accumulation of [3H]IP. Previous reports indicate that cytochalasin B enhances PMN activation in response to fMLP by increasing the production of inositol phosphates. Pretreatment of PMNs with cytochalasin B significantly enhanced O2- production in cells exposed to Aroclor 1242 but did not alter [H]IP accumulation. These data suggest that treatment of rat PMNs with Aroclor 1242 stimulates PI turnover and are consistent with the hypothesis that hydrolysis of membrane phospholipids is important in PMN activation by PCBs. The enhancing effect of cytochalasin B on PCB-induced O2- production, however, likely involves other mechanisms.

摘要

体外暴露于多氯联苯(PCBs)混合物Aroclor 1242可刺激大鼠多形核中性粒细胞(PMN)产生超氧阴离子(O2-)并脱颗粒。PCBs激活PMN的机制尚不清楚。磷脂酶C依赖的膜磷酸肌醇水解是PMN对包括N-甲酰甲硫氨酰亮氨酰苯丙氨酸(fMLP)在内的多种激动剂作出反应时激活的重要早期事件;因此,本研究旨在确定Aroclor 1242是否能刺激分离的大鼠PMN中肌醇磷酸的产生。用大鼠腹膜糖原诱导的PMN用肌醇-[2-3H]进行标记,并测定fMLP和Aroclor 1242对[3H]肌醇磷酸积累的影响。fMLP(在细胞松弛素B存在下)和Aroclor 1242均诱导含肌醇磷脂的快速分解。[3H]肌醇磷酸的峰值积累在Aroclor 1242作用后5秒内出现,在fMLP作用后15 - 30秒内出现。在细胞松弛素B处理的PMN中,暴露于fMLP或Aroclor 1242后5分钟内发生显著的O2-生成。2,2',4,4'-四氯联苯(TCB),而非3,3',4,4'-TCB,可刺激分离的大鼠PMN产生O2-并脱颗粒。为了确定肌醇磷酸积累是否与PMN激活平行,在LiCl处理的细胞中测量了对Aroclor 1242、2,2'4,4'-TCB和3,3'4,4'-TCB的反应中[3H]肌醇单磷酸(IP)的产生。Aroclor 1242和2,2',4,4'-TCB均导致[3H]IP的显著积累,而3,3',4,4'-TCB则无此作用。先前的报道表明,细胞松弛素B通过增加肌醇磷酸的产生来增强PMN对fMLP的激活。用细胞松弛素B预处理PMN可显著增强暴露于Aroclor 1242的细胞中的O2-产生,但不改变[H]IP的积累。这些数据表明,用Aroclor 1242处理大鼠PMN可刺激磷脂酰肌醇(PI)周转,并且与膜磷脂水解在PCBs激活PMN中起重要作用的假设一致。然而,细胞松弛素B对PCB诱导的O2-产生的增强作用可能涉及其他机制。

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