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通过透射电子显微镜鉴定细胞坏死和铁死亡的特征。

Identification of the hallmarks of necroptosis and ferroptosis by transmission electron microscopy.

机构信息

Department of Biochemistry, Toho University School of Medicine, 5-21-16 Omori-Nishi, Ota-ku, Tokyo, 143-8540, Japan.

Department of Cellular Molecular Neuropathology, Juntendo University Graduate School of Medicine, 2-1-1 Hongo, Bunkyo-ku, Tokyo, 113-8421, Japan.

出版信息

Biochem Biophys Res Commun. 2020 Jun 30;527(3):839-844. doi: 10.1016/j.bbrc.2020.04.127. Epub 2020 May 16.

Abstract

Apoptosis is the prototype for a regulated form of cell death, but recent studies have revealed other types of regulated forms of cell death, including necroptosis and ferroptosis. The molecular mechanisms underlying the execution of these processes have been intensively investigated, yet the hallmarks of their morphology are not fully understood. Here, we report that electron lucent cytoplasm was a common feature of both necroptosis and ferroptosis, which was consistent with cytoplasmic vacuolization due to a defect in the cytoplasmic membrane integrity. Notably, the perinuclear space was dilated in necroptosis, but such dilation did not occur in ferroptosis. Cells undergoing ferroptosis, but not necroptosis, exhibited an electron lucent nucleus. We previously reported that one of the nuclear danger-associated molecular patterns (DAMPs), high mobility group box (HMGB)1, is rapidly released from the nucleus to the extracellular spaces of cells undergoing necroptosis through the ruptured nuclear and cytoplasmic membrane. Via time-lapse imaging of cells stably expressing HMGB1 fused to a fluorescence protein, we found that HMGB1 was also released from the nucleus to the cytosol, and then eventually released into the extracellular spaces in cells undergoing ferroptosis. Thus, nuclear membrane damage was induced prior to cytoplasmic membrane rupture in ferroptosis. Thus, dilation of the perinuclear space and an electron lucent nucleus may be the hallmarks of necroptosis and ferroptosis, respectively.

摘要

细胞凋亡是一种受调控的细胞死亡形式的原型,但最近的研究揭示了其他类型的受调控的细胞死亡形式,包括坏死性凋亡和铁死亡。这些过程执行的分子机制已经得到了深入研究,但它们形态学的特征仍未完全理解。在这里,我们报告电子透明细胞质是坏死性凋亡和铁死亡的共同特征,这与细胞质膜完整性缺陷导致的细胞质空泡化一致。值得注意的是,坏死性凋亡中核周空间扩张,但铁死亡中没有发生这种扩张。发生铁死亡的细胞表现出电子透明核,而不是坏死性凋亡的细胞。我们之前报道过高迁移率族蛋白 B1(HMGB1)是一种核危险相关分子模式(DAMP)之一,它通过破裂的核和细胞质膜迅速从细胞核释放到坏死性凋亡细胞的细胞外空间。通过对稳定表达与荧光蛋白融合的 HMGB1 的细胞进行延时成像,我们发现 HMGB1 也从细胞核释放到细胞质中,然后最终在铁死亡的细胞中释放到细胞外空间。因此,铁死亡中先发生核膜损伤,然后发生细胞质膜破裂。因此,核周空间扩张和电子透明核可能分别是坏死性凋亡和铁死亡的特征。

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