GTP酶
鸟嘌呤核苷酸交换因子
细胞生物学
拉布
生物
肌动蛋白
CDC42型
细胞器
作者
Suli Zhang,Marcelo G. Kazanietz,Mariana Cooke
出处
期刊:American Journal of Physiology-cell Physiology
[American Physical Society]
日期:2020-08-26
卷期号:319 (5): C877-C884
被引量:32
标识
DOI:10.1152/ajpcell.00351.2020
摘要
Tunneling nanotubes (TNTs) emerged as important specialized actin-rich membrane protrusions for cell-to-cell communication. These structures allow the intercellular exchange of material, such as ions, soluble proteins, receptors, vesicles and organelles, therefore exerting critical roles in normal cell function. Indeed, TNTs participate in a number of physiological processes, including embryogenesis, immune response, and osteoclastogenesis. TNTs have been also shown to contribute to the transmission of retroviruses (e.g., human immunodeficiency virus-1, HIV-1) and coronaviruses. As with other membrane protrusions, the involvement of Rho GTPases in the formation of these elongated structures is undisputable, although the mechanisms involved are not yet fully elucidated. The tight control of Rho GTPase function by guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs) strongly suggests that localized control of these Rho regulators may contribute to TNT assembly and disassembly. Deciphering the intricacies of the complex signaling mechanisms leading to actin reorganization and TNT development would reveal important information about their involvement in normal cellular physiology as well as unveil potential targets for disease management.
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