Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada.
Department of Zoology, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada
J Neurosci. 2023 Mar 29;43(13):2260-2276. doi: 10.1523/JNEUROSCI.1323-22.2023. Epub 2023 Feb 17.
Glia are essential to protecting and enabling nervous system function and a key glial function is the formation of the glial sheath around peripheral axons. Each peripheral nerve in the larva is ensheathed by three glial layers, which structurally support and insulate the peripheral axons. How peripheral glia communicate with each other and between layers is not well established and we investigated the role of Innexins in mediating glial function in the periphery. Of the eight Innexins, we found two (Inx1 and Inx2) are important for peripheral glia development. In particular loss of Inx1 and Inx2 resulted in defects in the wrapping glia leading to disruption of the glia wrap. Of interest loss of Inx2 in the subperineurial glia also resulted in defects in the neighboring wrapping glia. Inx plaques were observed between the subperineurial glia and the wrapping glia suggesting that gap junctions link these two glial cell types. We found Inx2 is key to Ca pulses in the peripheral subperineurial glia but not in the wrapping glia, and we found no evidence of gap junction communication between subperineurial and wrapping glia. Rather we have clear evidence that Inx2 plays an adhesive and channel-independent role between the subperineurial and wrapping glia to ensure the integrity of the glial wrap. Gap junctions are critical for glia communication and formation of myelin in myelinating glia. However, the role of gap junctions in non-myelinating glia is not well studied, yet non-myelinating glia are critical for peripheral nerve function. We found the Innexin gap junction proteins are present between different classes of peripheral glia in Drosophila. Here Innexins form junctions to facilitate adhesion between the different glia but do so in a channel-independent manner. Loss of adhesion leads to disruption of the glial wrap around axons and leads to fragmentation of the wrapping glia membranes. Our work points to an important role for gap junction proteins in mediating insulation by non-myelinating glia.
胶质细胞对于保护和促进神经系统功能至关重要,其主要功能之一是在外周轴突周围形成胶质鞘。幼虫的每根周围神经都被三层胶质细胞包裹,这些细胞结构上支持和隔离外周轴突。然而,周围胶质细胞之间以及不同胶质层之间的通讯机制尚未得到充分阐明,我们研究了连接蛋白在介导周围胶质细胞功能中的作用。在这 8 种连接蛋白中,我们发现其中两种(Inx1 和 Inx2)对于外周胶质细胞的发育非常重要。具体来说,Inx1 和 Inx2 的缺失导致包裹胶质细胞的包裹缺陷,从而破坏了胶质包裹。有趣的是,亚神经胶质细胞中的 Inx2 缺失也导致相邻包裹胶质细胞的缺陷。我们观察到亚神经胶质细胞和包裹胶质细胞之间存在 Inx 斑,表明缝隙连接将这两种胶质细胞类型连接起来。我们发现 Inx2 对于周围亚神经胶质细胞中的 Ca 脉冲至关重要,但对于包裹胶质细胞则不然,并且我们没有发现亚神经胶质细胞和包裹胶质细胞之间存在缝隙连接通讯的证据。相反,我们有明确的证据表明,Inx2 在亚神经胶质细胞和包裹胶质细胞之间发挥着黏附和非通道依赖性的作用,以确保胶质包裹的完整性。缝隙连接对于胶质细胞通讯和形成髓鞘至关重要,但在非髓鞘形成胶质细胞中的作用尚未得到充分研究,然而,非髓鞘形成胶质细胞对于周围神经功能至关重要。我们发现,在果蝇的不同外周胶质细胞中存在连接蛋白间隙连接蛋白。在这里,连接蛋白形成连接,促进不同胶质细胞之间的黏附,但以非通道依赖性的方式进行。黏附的丧失导致围绕轴突的胶质包裹的破坏,并导致包裹胶质细胞的膜碎裂。我们的工作表明,间隙连接蛋白在介导非髓鞘形成胶质细胞的绝缘中起着重要作用。