Iyyathurai Jegan, Decuypere Jean-Paul, Leybaert Luc, D'hondt Catheleyne, Bultynck Geert
KU Leuven, Laboratory of Molecular and Cellular Signaling, Department Cellular and Molecular Medicine, Campus Gasthuisberg O/N-I bus 802, Herestraat 49, B-3000, Leuven, Belgium.
KU Leuven, Laboratory for Membrane Trafficking, Department of Human Genetics, and VIB-Center for the Biology of Disease, Campus Gasthuisberg, O/N-IV, 7.159, Herestraat 49, 3000, Leuven, Belgium.
BMC Cell Biol. 2016 May 24;17 Suppl 1(Suppl 1):20. doi: 10.1186/s12860-016-0093-9.
Connexins mediate intercellular communication by assembling into hexameric channel complexes that act as hemichannels and gap junction channels. Most connexins are characterized by a very rapid turn-over in a variety of cell systems. The regulation of connexin turn-over by phosphorylation and ubiquitination events has been well documented. Moreover, different pathways have been implicated in connexin degradation, including proteasomal and lysosomal-based pathways. Only recently, autophagy emerged as an important connexin-degradation pathway for different connexin isoforms. As such, conditions well known to induce autophagy have an immediate impact on the connexin-expression levels. This is not only limited to experimental conditions but also several pathophysiological conditions associated with autophagy (dys)function affect connexin levels and their presence at the cell surface as gap junctions. Finally, connexins are not only substrates of autophagy but also emerge as regulators of the autophagy process. In particular, several connexin isoforms appear to recruit pre-autophagosomal autophagy-related proteins, including Atg16 and PI3K-complex components, to the plasma membrane, thereby limiting their availability and capacity for regulating autophagy.
连接蛋白通过组装成六聚体通道复合物来介导细胞间通讯,这些复合物可作为半通道和间隙连接通道发挥作用。大多数连接蛋白的特点是在多种细胞系统中周转非常迅速。磷酸化和泛素化事件对连接蛋白周转的调节已有充分记录。此外,不同的途径参与了连接蛋白的降解,包括基于蛋白酶体和溶酶体的途径。直到最近,自噬才成为不同连接蛋白异构体的重要降解途径。因此,众所周知的诱导自噬的条件会立即影响连接蛋白的表达水平。这不仅限于实验条件,而且与自噬(功能)障碍相关的几种病理生理条件也会影响连接蛋白水平及其作为间隙连接在细胞表面的存在。最后,连接蛋白不仅是自噬的底物,而且还作为自噬过程的调节因子出现。特别是,几种连接蛋白异构体似乎将自噬前体自噬相关蛋白,包括Atg16和PI3K复合物成分,募集到质膜,从而限制了它们调节自噬的可用性和能力。