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豚鼠中性粒细胞的吞噬作用调节及溶酶体酶分泌:非甾体抗炎药和前列腺素的作用

Modulation of phagocytosis by and lysosomal enzyme secretion from guinea-pig neutrophils: effect of nonsteroid anti-inflammatory agents and prostaglindins.

作者信息

Smith R J

出版信息

J Pharmacol Exp Ther. 1977 Mar;200(3):647-57.

PMID:850132
Abstract

Guinea-pig neutrophils released lysosome granule-associated beta-glucuronidase, but not cytoplasmic lactate dehydrogenase during cell contact with and phagocytosis of serum-treated zymosan particles. Naproxen, chloroquine and indomethacin inhibited particle uptake by and lysosomal enzyme secretion from neutrophils incubated with zymosan in Krebs-Ringer phosphate medium, pH 7.4, at 37 degrees C. Acetylsalicyclic acid, fenoprofen and ibuprofen were inactive. Prostaglandins (PG) E1, E2, A1, A2, B1 and B2 reduced particle ingestion by and discharge of lysosomal enzymes from neutrophils. PGF2alpha accelerated lysosomal enzyme release, had no effect on phagocytosis at high concentrations and inhibited both processes at low concentrations.. PGF1alpha was inactive. In the presence of cytochalasin B, an agent which inhibits phagocytosis while havine no effect on selective lysosomal enzyme secretion, naproxen, chloroquine and indomethacin, continued to inhibit the discharge of beta-glucuronidase from neutrophils. PGE1, PGE2, PGA1, PGA2, PGB1 and PGB2 reduced lysosomal enzyme release from cytochalasin B-treated neutrophils. PGF2alpha accelerated at high and inhibited at low concentrations the selective secretion of beta-glucuronidase from cytochalasin B-treated neutrophils. PGF1alpha was again inactive. These studies indicated that guinea-pig neutrophils are capable of a selective release of lysosomal enzymes (beta-glucuronidase) during ingestion of serum-treated zymosan particles and that certain anti-inflammatory drugs and prostaglansins may function as modulators of the phagocytic release of lysosomal enzymes from neutrophils.

摘要

豚鼠中性粒细胞在与经血清处理的酵母聚糖颗粒接触及吞噬过程中,会释放溶酶体颗粒相关的β-葡萄糖醛酸酶,但不会释放细胞质中的乳酸脱氢酶。萘普生、氯喹和吲哚美辛可抑制在pH 7.4、37℃的 Krebs-Ringer 磷酸盐培养基中与酵母聚糖一起孵育的中性粒细胞对颗粒的摄取以及溶酶体酶的分泌。乙酰水杨酸、非诺洛芬和布洛芬则无此作用。前列腺素(PG)E1、E2、A1、A2、B1和B2可减少中性粒细胞对颗粒的摄取以及溶酶体酶的释放。PGF2α可加速溶酶体酶的释放,高浓度时对吞噬作用无影响,低浓度时则抑制这两个过程。PGF1α无活性。在细胞松弛素B存在的情况下(细胞松弛素B是一种抑制吞噬作用但对选择性溶酶体酶分泌无影响的药物),萘普生、氯喹和吲哚美辛仍可抑制中性粒细胞释放β-葡萄糖醛酸酶。PGE1、PGE2、PGA1、PGA2、PGB1和PGB2可减少经细胞松弛素B处理的中性粒细胞释放溶酶体酶。PGF2α在高浓度时可加速经细胞松弛素B处理的中性粒细胞选择性分泌β-葡萄糖醛酸酶,在低浓度时则抑制该过程。PGF1α再次显示无活性。这些研究表明,豚鼠中性粒细胞在摄取经血清处理的酵母聚糖颗粒过程中能够选择性释放溶酶体酶(β-葡萄糖醛酸酶),并且某些抗炎药物和前列腺素可能作为中性粒细胞吞噬性释放溶酶体酶的调节剂发挥作用。

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