《生命科学》 2022, 34(4): 392-400
免疫原性微核的起源与生物医学意义
摘 要:
微核(micronuclei, MN) 是独立于细胞核的小型类核结构,常见于肿瘤细胞。MN 在结构和遗传活性方面表现出巨大异质性,相当部分的MN 具有结构缺陷且倾向于破裂的核被膜(micronuclear envelope, mNE)。mNE 破裂后,MN 可启动染色体碎裂和固有免疫通路,暗示免疫原性MN (immunogenic MN, iMN)具有广泛的生物医学意义。该文首先讨论MN 的起源、mNE 易破裂的结构基础以及两个主要的分子和细胞模型,随后梳理出MN 破裂后诱发染色体碎裂与激活cGAS-STING 固有免疫通路的分子过程,最后总结了iMN 在抗肿瘤活性和促肿瘤演化过程中所表现出的复杂作用及相应机制。iMN 的研究为MN 领域注入了全新的学术理论和思想。解析mNE 不稳定的分子与结构基础以及iMN 对肿瘤双向作用(iMN 悖论) 的机制将是未来几年细胞生物学和遗传学领域的研究热点之一。
通讯作者:郭锡汉 , Email:guo_xihan@163.com
Abstract:
Micronuclei (MN) are small nucleus-like structures separated from the nucleus. MN are common in tumor cells and display a great heterogeneity in their structure and genetic activity. Due to the structural defects, micronuclear envelope (mNE) is rather prone to rupture, which triggers chromothripsis and innate immune responses. These findings suggest that immunogenic MN (iMN) has a wide range of biomedical implications. In this review, we firstly discuss the origin of MN, the structural basis of rupture-prone mNE, and two molecular and cellular models underlying mNE structural defects. Secondly, we explore the molecular mechanisms contributing to the induction of chromothripsis and activation of cGAS-STING innate immune pathway in ruptured MN. Finally, we summary the complicated roles and the corresponding mechanisms of iMN in suppressing tumor growth and promoting tumor evolution. As a new chapter in MN field, iMN has brought us new academic theories and ideas about MN. Dissecting the complexities of the molecular and structural origins of mNE instability, as well as the mechanisms for the dual roles of iMN in tumor (that is, iMN paradox), will be one of next frontiers in the fields of cell biology and genetics in the upcoming years.
Communication Author:GUO Xi-Han , Email:guo_xihan@163.com