Subedi Yagya P, Altenberg Guillermo A, Chang Cheng-Wei T
Department of Chemistry & Biochemistry, Utah State University, 0300 Old Main Hill, Logan, UT 84322-0300, USA.
Department of Cell Physiology & Molecular Biophysics, & Center for Membrane Protein Research, Texas Tech University Health Sciences Center, Lubbock, TX 79430-6551, USA.
Future Med Chem. 2021 Feb;13(4):379-392. doi: 10.4155/fmc-2020-0291. Epub 2021 Jan 5.
Gap-junction channels formed by two connexin hemichannels play diverse and pivotal roles in intercellular communication and regulation. Normally hemichannels at the plasma membrane participate in autocrine and paracrine signaling, but abnormal increase in their activity can lead or contribute to various diseases. Selective inhibitors toward connexin hemichannels are of great interest. Among more than 20 identified isoforms of connexins, connexin 43 (Cx43) attracts the most interest due to its prevalence and link to cell damage in many disorders or diseases. Traditional antibacterial kanamycin decorated with hydrophobic groups yields amphiphilic kanamycins that show low cytotoxicity and prominent inhibitory effect against Cx43. This review focuses on the development of amphiphilic kanamycins as connexin hemichannel inhibitors and their future perspective.
由两个连接蛋白半通道形成的间隙连接通道在细胞间通讯和调节中发挥着多样且关键的作用。正常情况下,质膜上的半通道参与自分泌和旁分泌信号传导,但它们活性的异常增加会导致或促成各种疾病。针对连接蛋白半通道的选择性抑制剂备受关注。在已鉴定出的20多种连接蛋白亚型中,连接蛋白43(Cx43)因其普遍性以及与许多病症或疾病中的细胞损伤的关联而最受关注。用疏水基团修饰的传统抗菌卡那霉素可产生两亲性卡那霉素,其具有低细胞毒性且对Cx43有显著抑制作用。本综述重点关注两亲性卡那霉素作为连接蛋白半通道抑制剂的研发及其未来前景。