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肿瘤坏死因子相关凋亡诱导配体(TRAIL)在巨核细胞和血小板中的表达。

Expression of TNF-related apoptosis-inducing ligand (TRAIL) in megakaryocytes and platelets.

作者信息

Crist Scott A, Elzey Bennett D, Ludwig Aaron T, Griffith Thomas S, Staack Jeffrey B, Lentz Steven R, Ratliff Timothy L

机构信息

Department of Urology, The University of Iowa, Iowa City, Iowa 52242-1089, USA.

出版信息

Exp Hematol. 2004 Nov;32(11):1073-81. doi: 10.1016/j.exphem.2004.07.022.

Abstract

OBJECTIVE

Platelets are known to play an important role in hemostasis, thrombosis, wound healing, and inflammation. Platelet-induced modulation of inflammation and adaptive immune responses are mediated in part through tumor necrosis factor (TNF) family member ligands, including CD154, Fas ligand, and TNFalpha, that are expressed upon platelet activation. The present study investigated whether platelets and megakaryocytes also express TNF-related apoptosis-inducing ligand (TRAIL), another pro-apoptotic member of the TNF superfamily.

MATERIALS AND METHODS

Immunoprecipitation, enzyme-linked immunosorbent assay, and flow cytometry were used to assess TRAIL protein expression on isolated platelets, in vitro-derived megakaryocytes and premegakaryocyte cell lines. Reverse-transcription polymerase chain reaction and transient transfection of TRAIL promoter/reporter constructs were used to elucidate mechanisms of TRAIL regulation during megakaryocyte differentiation. TRAIL-dependent cytotoxicity assays were performed to determine if platelet-derived TRAIL induces apoptosis of TRAIL sensitive target cells.

RESULTS

Activated platelets expressed both membrane-bound and soluble TRAIL. TRAIL was also expressed by megakaryocytes, and in vitro studies showed that TRAIL expression was induced upon megakaryocyte differentiation. TRAIL expression was mediated by increased transcriptional activity of the TRAIL promoter, suggesting lineage-specific regulation of TRAIL during megakaryocyte differentiation. Abundant detergent-extractable, full-length TRAIL protein was observed in the lysates of platelets and megakaryocytes, but only low concentrations of TRAIL were released by nondetergent extraction methods.

CONCLUSION

The data reported herein show that platelets express TRAIL that is synthesized by megakaryocytes and was expressed by activated platelets. While these data expand the spectrum of TNF family proteins expressed in platelets, the function of platelet-derived TRAIL is not known.

摘要

目的

已知血小板在止血、血栓形成、伤口愈合和炎症中发挥重要作用。血小板诱导的炎症调节和适应性免疫反应部分是通过肿瘤坏死因子(TNF)家族成员配体介导的,包括CD154、Fas配体和TNFα,这些配体在血小板激活时表达。本研究调查血小板和巨核细胞是否也表达TNF相关凋亡诱导配体(TRAIL),这是TNF超家族的另一个促凋亡成员。

材料与方法

采用免疫沉淀、酶联免疫吸附测定和流式细胞术评估分离的血小板、体外衍生的巨核细胞和前巨核细胞系上TRAIL蛋白的表达。使用逆转录聚合酶链反应和TRAIL启动子/报告基因构建体的瞬时转染来阐明巨核细胞分化过程中TRAIL调节的机制。进行TRAIL依赖性细胞毒性测定以确定血小板衍生的TRAIL是否诱导TRAIL敏感靶细胞的凋亡。

结果

活化的血小板表达膜结合型和可溶性TRAIL。巨核细胞也表达TRAIL,体外研究表明,巨核细胞分化时TRAIL表达被诱导。TRAIL表达是由TRAIL启动子转录活性增加介导的,提示巨核细胞分化过程中TRAIL的谱系特异性调节。在血小板和巨核细胞的裂解物中观察到大量可被去污剂提取的全长TRAIL蛋白,但非去污剂提取方法仅释放低浓度的TRAIL。

结论

本文报道的数据表明,血小板表达由巨核细胞合成并在活化血小板中表达的TRAIL。虽然这些数据扩展了血小板中表达的TNF家族蛋白的范围,但血小板衍生的TRAIL的功能尚不清楚。

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