Wright J W, Copenhaver P F
Department of Cell and Developmental Biology L-215, Oregon Health Sciences University, 3181 SW Sam Jackson Park Road, Portland, Oregon 97201, USA.
Dev Biol. 2001 Jun 1;234(1):24-41. doi: 10.1006/dbio.2001.0247.
During the formation of the insect peripheral nervous system (PNS), the cell adhesion receptor fasciclin II has been shown to play a prominent role in axonal fasciculation and synapse formation during motor neuron outgrowth. In the moth Manduca, fasciclin II (MFas II) is expressed both as a transmembrane isoform (TM-MFas II) and a glycosyl phosphatidylinositol-linked isoform (GPI-MFas II). By using RNA and antibody probes, we have shown that these two isoforms are expressed in nonoverlapping patterns: TM-MFas II is expressed exclusively by neurons and becomes localized to their most motile regions, while GPI-MFas II is expressed primarily by the glial cells that ensheath the peripheral nerves. This cell-type specificity of expression allowed us to monitor the nature of neuronal-glial interactions during PNS development. The outgrowth of TM-MFas II-positive axons in many regions preceded the arrival of GPI-MFas II-expressing glial processes that enwrapped them. In a few key locations, however, GPI-MFas II-positive glial cells differentiated before the arrival of the first axons and prefigured their subsequent trajectories. Prior inhibition of GPI-MFas II expression disrupted the subsequent outgrowth of axons at these locations but not elsewhere in the PNS. Our results suggest that the two isoforms of MFas II play distinct roles with respect to cellular motility and nerve formation.
在昆虫外周神经系统(PNS)形成过程中,细胞黏附受体 fasciclin II 已被证明在运动神经元生长过程中的轴突成束和突触形成中发挥着重要作用。在烟草天蛾中,fasciclin II(MFas II)以跨膜异构体(TM-MFas II)和糖基磷脂酰肌醇连接异构体(GPI-MFas II)两种形式表达。通过使用 RNA 和抗体探针,我们发现这两种异构体以不重叠的模式表达:TM-MFas II 仅由神经元表达,并定位于其最活跃的区域,而 GPI-MFas II 主要由包裹外周神经的神经胶质细胞表达。这种表达的细胞类型特异性使我们能够监测 PNS 发育过程中神经元与神经胶质细胞相互作用的性质。在许多区域,TM-MFas II 阳性轴突的生长先于包裹它们的 GPI-MFas II 表达的神经胶质突起的到达。然而,在一些关键位置,GPI-MFas II 阳性神经胶质细胞在第一批轴突到达之前就已分化,并预先确定了它们随后的轨迹。事先抑制 GPI-MFas II 的表达会破坏这些位置轴突的后续生长,但不会影响 PNS 其他部位的轴突生长。我们的结果表明,MFas II 的两种异构体在细胞运动性和神经形成方面发挥着不同的作用。