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膜近端肿瘤坏死因子相关凋亡诱导配体(TRAIL)分子不能诱导短路凋亡信号:对药物开发和基础细胞因子生物学的启示。

Membrane-proximal TRAIL species are incapable of inducing short circuit apoptosis signaling: Implications for drug development and basic cytokine biology.

作者信息

Tatzel Katharina, Kuroki Lindsay, Dmitriev Igor, Kashentseva Elena, Curiel David T, Goedegebuure S Peter, Powell Matthew A, Mutch David G, Hawkins William G, Spitzer Dirk

机构信息

Washington University School of Medicine, Department of Surgery, 660 S. Euclid Avenue, St. Louis, Missouri 63110, USA.

Washington University School of Medicine, Division of Gynecologic Oncology, 660 S. Euclid Avenue, St. Louis, Missouri 63110, USA.

出版信息

Sci Rep. 2016 Mar 3;6:22661. doi: 10.1038/srep22661.

Abstract

TRAIL continues to garner substantial interest as a recombinant cancer therapeutic while the native cytokine itself serves important tumor surveillance functions when expressed in membrane-anchored form on activated immune effector cells. We have recently developed the genetically stabilized TRAIL platform TR3 in efforts to improve the limitations associated with currently available drug variants. While in the process of characterizing mesothelin-targeted TR3 variants using a single chain antibody (scFv) delivery format (SS-TR3), we discovered that the membrane-tethered cytokine had a substantially increased activity profile compared to non-targeted TR3. However, cell death proceeded exclusively via a bystander mechanism and protected the mesothelin-positive targets from apoptosis rather than leading to their elimination. Incorporation of a spacer-into the mesothelin surface antigen or the cancer drug itself-converted SS-TR3 into a cis-acting phenotype. Further experiments with membrane-anchored TR3 variants and the native cytokine confirmed our hypothesis that membrane-proximal TRAIL species lack the capacity to physically engage their cognate receptors coexpressed on the same cell membrane. Our findings not only provide an explanation for the "peaceful" coexistence of ligand and receptor of a representative member of the TNF superfamily but give us vital clues for the design of activity-enhanced TR3-based cancer therapeutics.

摘要

肿瘤坏死因子相关凋亡诱导配体(TRAIL)作为一种重组癌症治疗药物,持续引起了广泛关注,而天然细胞因子本身在活化的免疫效应细胞上以膜锚定形式表达时,发挥着重要的肿瘤监视功能。我们最近开发了基因稳定的TRAIL平台TR3,以努力改善与目前可用药物变体相关的局限性。在使用单链抗体(scFv)递送形式(SS-TR3)对间皮素靶向的TR3变体进行表征的过程中,我们发现与非靶向TR3相比,膜 tethered 细胞因子的活性谱有显著增加。然而,细胞死亡仅通过旁观者机制进行,保护间皮素阳性靶标免于凋亡,而不是导致它们被消除。将间隔物掺入间皮素表面抗原或癌症药物本身,将SS-TR3转变为顺式作用表型。对膜锚定的TR3变体和天然细胞因子进行的进一步实验证实了我们的假设,即膜近端的TRAIL种类缺乏与在同一细胞膜上共表达的同源受体进行物理结合的能力。我们的发现不仅为肿瘤坏死因子超家族代表性成员的配体和受体的“和平”共存提供了解释,而且为设计基于TR3的活性增强型癌症治疗药物提供了重要线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ea8/4776141/04beed44a6f6/srep22661-f2.jpg

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