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中间体及中间体残余物:从细胞碎片到具有诊断和治疗潜力的信号细胞器

The midbody and midbody remnant: from cellular debris to signaling organelle with diagnostic and therapeutic potential.

作者信息

Kuriyama Ryoko, Mullins J Michael, Skop Ahna R

机构信息

Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455.

Department of Biology, The Catholic University of America, Washington, DC 20064.

出版信息

Mol Biol Cell. 2025 Jul 1;36(7):re4. doi: 10.1091/mbc.E25-03-0120. Epub 2025 May 28.

DOI:10.1091/mbc.E25-03-0120
PMID:40434898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12260166/
Abstract

The midbody (MB), a transient structure formed during cytokinesis, has evolved from a mere structural component to a complex signaling organelle with diverse functions beyond cell division. Recent studies have revealed that jettisoned MB remnants (MBR) play crucial roles in intercellular communication, influencing cell fate decisions, particularly in stem cells and cancer. MBRs act as large extracellular vesicles, transferring functional RNA and proteins that modulate cell behavior, including proliferation and cancer progression. The protein KIF23, associated with MBs, is a pan-cancer marker, underscoring the clinical relevance of MB research. This review highlights the emerging significance of MBs and MBRs in cancer biology, neurobiology, and regenerative medicine, offering new avenues for diagnostic and therapeutic strategies. By reshaping our understanding of cell division and intercellular communication, these findings open exciting frontiers in cell biology with huge potential for diagnostic and therapeutic applications.

摘要

中间体(MB)是细胞分裂过程中形成的一种短暂结构,它已从一个单纯的结构成分演变成一个复杂的信号细胞器,具有超越细胞分裂的多种功能。最近的研究表明,被抛弃的中间体残余物(MBR)在细胞间通讯中发挥着关键作用,影响细胞命运决定,尤其是在干细胞和癌症中。MBR作为大型细胞外囊泡,转运调节细胞行为(包括增殖和癌症进展)的功能性RNA和蛋白质。与中间体相关的蛋白KIF23是一种泛癌标志物,突出了中间体研究的临床相关性。本综述强调了中间体和MBR在癌症生物学、神经生物学和再生医学中日益凸显的重要性,为诊断和治疗策略提供了新途径。通过重塑我们对细胞分裂和细胞间通讯的理解,这些发现为细胞生物学开辟了令人兴奋的前沿领域,在诊断和治疗应用方面具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/7aefc90715d6/nihms-2096709-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/d2f6034466c5/nihms-2096709-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/4aa580c154d4/nihms-2096709-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/7aefc90715d6/nihms-2096709-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/d2f6034466c5/nihms-2096709-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/4aa580c154d4/nihms-2096709-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c43/12302901/7aefc90715d6/nihms-2096709-f0003.jpg

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本文引用的文献

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EMBO J. 2025 Jan;44(2):331-355. doi: 10.1038/s44318-024-00327-7. Epub 2024 Dec 4.
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Extracellular vesicles, including large translating vesicles called midbody remnants, are released during the cell cycle.细胞外囊泡,包括称为中间体残余物的大型翻译囊泡,在细胞周期中释放。
Mol Biol Cell. 2024 Dec 1;35(12):ar155. doi: 10.1091/mbc.E23-10-0384. Epub 2024 Nov 13.
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Long-term three-dimensional high-resolution imaging of live unlabeled small intestinal organoids via low-coherence holotomography.
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Exp Mol Med. 2024 Oct;56(10):2162-2170. doi: 10.1038/s12276-024-01312-0. Epub 2024 Oct 1.
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Targeting SHCBP1 Inhibits Tumor Progression by Restoring Ciliogenesis in Ductal Carcinoma.靶向SHCBP1通过恢复导管癌中的纤毛发生来抑制肿瘤进展。
Cancer Res. 2024 Dec 16;84(24):4156-4172. doi: 10.1158/0008-5472.CAN-24-1095.
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Bioinformatics Analysis Screening and Identification of Key Biomarkers and Drug Targets in Human Glioblastoma.人胶质母细胞瘤关键生物标志物和药物靶点的生物信息学分析筛选与鉴定
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