The Vanderbilt Eye Institute and Vanderbilt Brain Institute, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Proc Natl Acad Sci U S A. 2010 Mar 16;107(11):5196-201. doi: 10.1073/pnas.0913141107. Epub 2010 Mar 1.
An early hallmark of neuronal degeneration is distal transport loss and axon pathology. Glaucoma involves the degeneration of retinal ganglion cell (RGC) neurons and their axons in the optic nerve. Here we show that, like other neurodegenerations, distal axon injury appears early in mouse glaucoma. Where RGC axons terminate in the superior colliculus, reduction of active transport follows a retinotopic pattern resembling glaucomatous vision loss. Like glaucoma, susceptibility to transport deficits increases with age and is not necessarily associated with elevated ocular pressure. Transport deficits progress distal-to-proximal, appearing in the colliculus first followed by more proximal secondary targets and then the optic tract. Transport persists through the optic nerve head before finally failing in the retina. Although axon degeneration also progresses distal-to-proximal, myelinated RGC axons and their presynaptic terminals persist in the colliculus well after transport fails. Thus, distal transport loss is predegenerative and may represent a therapeutic target.
神经元变性的早期标志是远端运输损失和轴突病变。青光眼涉及视网膜神经节细胞 (RGC) 神经元及其视神经中的轴突变性。在这里,我们表明,与其他神经退行性疾病一样,远端轴突损伤在小鼠青光眼早期就出现了。在 RGC 轴突终止于上丘的地方,活性运输的减少遵循类似于青光眼视力丧失的视网膜拓扑模式。与青光眼一样,对运输缺陷的易感性随年龄增长而增加,并且不一定与眼压升高有关。运输缺陷从远端到近端进展,首先在上丘出现,然后是更近端的次要靶标,然后是视神经。运输在视神经头部通过,最后在视网膜失败。尽管轴突变性也从远端到近端进展,但髓鞘化的 RGC 轴突及其突触前末端在上丘中仍然存在,即使在运输失败之后。因此,远端运输损失是退行性前的,可能代表一个治疗靶点。