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用链状裸甲藻麻痹性贝类毒素诱导狮爪扇贝血细胞凋亡。

Apoptosis of hemocytes from lions-paw scallop Nodipecten subnodosus induced with paralyzing shellfish poison from Gymnodinium catenatum.

作者信息

Estrada Norma, Ascencio Felipe, Shoshani Liora, Contreras Rubén G

机构信息

Centro de Investigaciones Biológicas del Noroeste, S.C. (CIBNOR), Calle IPN #195, La Paz, B.C.S. 23096, Mexico.

Centro de Investigaciones Biológicas del Noroeste, S.C. (CIBNOR), Calle IPN #195, La Paz, B.C.S. 23096, Mexico.

出版信息

Immunobiology. 2014 Dec;219(12):964-74. doi: 10.1016/j.imbio.2014.07.006. Epub 2014 Jul 22.

DOI:10.1016/j.imbio.2014.07.006
PMID:25097151
Abstract

The toxic dinoflagellate Gymnodinium catenatum produces paralyzing shellfish poisons (PSPs) that are consumed and accumulated by bivalves. Previously, we recorded a decrease in hemocytes 24h after injection of PSPs (gonyautoxin 2/3 epimers, GTX2/3) in the adductor muscle in the lions-paw scallop Nodipecten subnodosus. In this work, qualitative and quantitative analyses, in in vivo and in vitro experiments, revealed that the lower count of hemocytes results from cells undergoing typical apoptosis when exposed to GTX 2/3 epimers. This includes visible morphological alterations of the cytoplasmic membrane, damage to the nuclear membrane, condensation of chromatin, DNA fragmentation, and release of DNA fragments into the cytoplasm. Induction of apoptosis was accompanied by phosphatidylserine exposure to the outer cell membrane and activation of cysteine-aspartic proteases, caspase 3 and caspase 8. Addition of an inhibitor of caspase to the medium suppressed activation in hemocytes exposed to the toxins, suggesting that cell death was induced by a caspase-dependent apoptotic pathway. The results are important for future investigation of the scallop's immune system and should provide new insights into apoptotic processes in immune cells of scallops exposed to PSPs.

摘要

有毒的甲藻链状裸甲藻产生麻痹性贝类毒素(PSP),双壳贝类会摄取并积累这些毒素。此前,我们记录到在狮爪扇贝(Nodipecten subnodosus)的闭壳肌中注射PSP(膝沟藻毒素2/3差向异构体,GTX2/3)24小时后血细胞数量减少。在这项研究中,体内和体外实验的定性与定量分析表明,血细胞数量减少是由于细胞在接触GTX 2/3差向异构体时发生了典型的凋亡。这包括细胞膜明显的形态改变、核膜损伤、染色质凝聚、DNA片段化以及DNA片段释放到细胞质中。凋亡的诱导伴随着磷脂酰丝氨酸暴露于细胞膜外以及半胱天冬酶3和半胱天冬酶8的激活。向培养基中添加半胱天冬酶抑制剂可抑制暴露于毒素的血细胞的激活,这表明细胞死亡是由半胱天冬酶依赖性凋亡途径诱导的。这些结果对于未来研究扇贝的免疫系统具有重要意义,并应为了解暴露于PSP的扇贝免疫细胞中的凋亡过程提供新的见解。

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