Department of Systems Pharmacology and Translational Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Medicine, Einstein Medical Center Philadelphia, Philadelphia, Pennsylvania.
Am J Physiol Cell Physiol. 2020 Nov 1;319(5):C877-C884. doi: 10.1152/ajpcell.00351.2020. Epub 2020 Aug 26.
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.
隧道纳米管(TNTs)作为细胞间通讯的重要的特殊的富含肌动蛋白的膜突,已经出现。这些结构允许细胞间物质的交换,如离子、可溶性蛋白、受体、囊泡和细胞器,因此在正常细胞功能中发挥着关键作用。事实上,TNTs 参与了许多生理过程,包括胚胎发生、免疫反应和破骨细胞生成。隧道纳米管也被证明有助于逆转录病毒(例如,人类免疫缺陷病毒-1,HIV-1)和冠状病毒的传播。与其他膜突一样,Rho GTPases 在这些伸长结构的形成中起作用是无可争议的,尽管涉及的机制尚未完全阐明。鸟嘌呤核苷酸交换因子(GEFs)和 GTPase 激活蛋白(GAPs)对 Rho GTPase 功能的严格控制强烈表明,这些 Rho 调节剂的局部控制可能有助于 TNT 的组装和拆卸。破译导致肌动蛋白重排和 TNT 发育的复杂信号机制的复杂性,将揭示它们在正常细胞生理学中的参与的重要信息,并揭示疾病管理的潜在目标。