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钙离子载体A23187诱导人嗜酸性粒细胞发生钙依赖性溶细胞脱颗粒。

Calcium ionophore A23187 calcium-dependent cytolytic degranulation in human eosinophils.

作者信息

Fukuda T, Ackerman S J, Reed C E, Peters M S, Dunnette S L, Gleich G J

出版信息

J Immunol. 1985 Aug;135(2):1349-56.

PMID:3925008
Abstract

The divalent cation ionophore A23187 is frequently used for studies of eosinophil degranulation. Nonetheless, the mechanism whereby A23187 induces degranulation in human eosinophils is still unclear. In the present experiments, A23187 caused human eosinophils to release a granule protein, eosinophil-derived neurotoxin (EDN) and a membrane-associated protein, Charcot-Leyden crystal (CLC) protein in a calcium and a concentration-dependent manner. However, A23187 at a concentration (1 microgram/ml) that caused 15% EDN release and 30% CLC protein release also produced release of the cytoplasmic enzyme lactic dehydrogenase (LDH) and loss of cell viability, both of which were calcium dependent. CLC protein release preceded EDN release and was detectable even at 15 min after the addition of 1 microgram/ml A23187, whereas EDN release occurred after a lag period of 30 min, and coincided with LDH release. At 1 microgram/ml A23187, neither the release of LDH nor the loss of viability occurred with purified neutrophils obtained in the same blood sample as a by-product of eosinophil purification. Electron microscopic examination demonstrated that exposure to A23187 for 15 min resulted in an increase and elongation of microridges on the cell surface, and exposure for 45 min caused cell disruption followed by extrusion of membrane-bound granules through breaks in the plasma membrane. Only once was granule exocytosis observed. These results indicate that A23187 treatment of eosinophils causes an initial release of membrane-associated CLC protein by a noncytolytic mechanism, and causes degranulation as a result of eosinophil lysis.

摘要

二价阳离子载体A23187常用于嗜酸性粒细胞脱颗粒的研究。然而,A23187诱导人嗜酸性粒细胞脱颗粒的机制仍不清楚。在本实验中,A23187以钙和浓度依赖的方式导致人嗜酸性粒细胞释放颗粒蛋白嗜酸性粒细胞衍生神经毒素(EDN)和膜相关蛋白夏科-莱登结晶(CLC)蛋白。然而,浓度为1微克/毫升的A23187在导致15%的EDN释放和30%的CLC蛋白释放的同时,也导致细胞质酶乳酸脱氢酶(LDH)的释放和细胞活力的丧失,这两者均依赖于钙。CLC蛋白的释放在EDN释放之前,即使在加入1微克/毫升A23187后15分钟也可检测到,而EDN释放则在30分钟的延迟期后发生,并与LDH释放同时出现。在1微克/毫升的A23187浓度下,与作为嗜酸性粒细胞纯化副产品从同一血样中获得的纯化中性粒细胞未发生LDH释放和活力丧失。电子显微镜检查显示,暴露于A23187 15分钟导致细胞表面微嵴增加和伸长,暴露45分钟导致细胞破裂,随后膜结合颗粒通过质膜破裂挤出。仅观察到一次颗粒胞吐作用。这些结果表明,用A23187处理嗜酸性粒细胞会通过非溶细胞机制导致膜相关CLC蛋白的初始释放,并由于嗜酸性粒细胞溶解而导致脱颗粒。

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