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淋巴细胞介导的细胞毒性的分子机制。

Molecular mechanisms of lymphocyte-mediated cytotoxicity.

作者信息

Fan Zusen, Zhang Qixiang

机构信息

National Laboratory of Biomacromolecules, Center for Infection and Immunity, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Cell Mol Immunol. 2005 Aug;2(4):259-64.

Abstract

Granule-mediated cytotoxicity is the major mechanism for lymphocytes to kill viruses, intracellular bacteria and tumors. The cytotoxic granules move to the immunological synapse by exocytosis after recognition of a killer cell. The contents of the granules are delivered into target cells with the help of perforin by endocytosis. A group of serine protease granzymes cleave their critical substrates to initiate DNA damage and cell death. The most abundant granzymes are granzyme A and B. They induce cell death through alternate and nonoverlapping pathways. The substrates and functions of the majority of the orphan granzymes have not yet been identified. It is possible that the diversity of granzymes provides fail-safe mechanisms for killing viruses and tumor cells.

摘要

颗粒介导的细胞毒性是淋巴细胞杀死病毒、细胞内细菌和肿瘤的主要机制。杀伤细胞识别后,细胞毒性颗粒通过胞吐作用移动到免疫突触。颗粒内容物在内皮素的帮助下通过内吞作用传递到靶细胞中。一组丝氨酸蛋白酶颗粒酶切割其关键底物以引发DNA损伤和细胞死亡。最丰富的颗粒酶是颗粒酶A和B。它们通过交替且不重叠的途径诱导细胞死亡。大多数孤儿颗粒酶的底物和功能尚未确定。颗粒酶的多样性可能为杀死病毒和肿瘤细胞提供了安全保障机制。

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