Jin Ying, Ziemba Kristine S, Smith George M
Department of Physiology, Spinal Cord and Brain Injury Research Center, University of Kentucky, Lexington, KY 40536, USA.
Exp Neurol. 2008 Apr;210(2):521-30. doi: 10.1016/j.expneurol.2007.11.030. Epub 2007 Dec 23.
Our previous studies showed that axonal outgrowth from dorsal root ganglia (DRG) transplants in the adult rat brain could be directed toward a specific target location using a preformed growth-supportive pathway. This pathway induced axon growth within the corpus callosum across the midline to the opposite hemisphere. In this study, we examined whether such pathways would also support axon growth either through or around a lesion of the corpus callosum. Pathways expressing GFP, NGF, or FGF2/NGF were set up by multiple injections of adenovirus along the corpus callosum. Each pathway included the transplantation site in the left corpus callosum, 2.8 mm away from the midline, and a target site in the right corpus callosum, 2.5 mm from the midline. At the same time, a 1 mm lesion was made through the corpus callosum at the midline in an anteroposterior direction. A group of control animals received lesions and Ad-NGF injections only at the transplant and target sites, without a bridging pathway. DRG cell suspensions from postnatal day 1 or 2 rats were injected at the transplantation site three to four days later. Two weeks after transplantation, brain sections were stained using an anti-CGRP antibody. The CGRP+ axons were counted at 0.5 mm and 1.5 mm from the lesion site in both hemispheres. Few axons grew past the lesion in animals with control pathways, but there was robust axon growth across the lesion site in the FGF2/NGF and NGF-expressing pathways. This study indicated that preformed NGF and combination guidance pathways support more axon growth past a lesion in the adult mammalian brain.
我们之前的研究表明,在成年大鼠大脑中,背根神经节(DRG)移植产生的轴突生长可以通过预先形成的生长支持通路导向特定的目标位置。该通路诱导胼胝体内的轴突生长穿过中线到达对侧半球。在本研究中,我们检查了这样的通路是否也能支持轴突在胼胝体损伤部位穿过或绕过损伤部位生长。通过沿胼胝体多次注射腺病毒来建立表达绿色荧光蛋白(GFP)、神经生长因子(NGF)或成纤维细胞生长因子2/神经生长因子(FGF2/NGF)的通路。每条通路包括左胼胝体中距中线2.8毫米处的移植部位和右胼胝体中距中线2.5毫米处的目标部位。与此同时,在胼胝体中线处从前向后制作一个1毫米的损伤。一组对照动物仅在移植部位和目标部位接受损伤和Ad-NGF注射,没有桥接通路。出生后第1天或第2天大鼠的DRG细胞悬液在3至4天后注射到移植部位。移植后两周,使用抗降钙素基因相关肽(CGRP)抗体对脑切片进行染色。在两个半球中距损伤部位0.5毫米和1.5毫米处计数CGRP+轴突。在具有对照通路的动物中,很少有轴突生长越过损伤部位,但在表达FGF2/NGF和NGF的通路中,有大量轴突生长穿过损伤部位。这项研究表明,预先形成的NGF和联合引导通路支持成年哺乳动物大脑中更多的轴突生长越过损伤部位。